Anusha Purushotham - Final Research Report - 171114.pdf
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Understanding the barriers experienced
by the people of an urban slum in
Bangalore to access the primary
diabetes and hypertension care
facilitated by the Institute of Public
Health (IPH)
Name: Anusha Purushotham
IPH Supervisors: Dr. Mrunalini Gowda, Dr. Narayanan Devadasan, Dr. Thriveni
BS
SOCHARA Supervisors: Dr. Rahul ASGR and Mr. Sabu KU
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Table of Contents
Study details…………………………………………………………………………………………………………………… 1
Background…………………………………………………………………………………………………………………….. 2 – 8
Aim and Objectives……………………………………………………………………………………………………...... 9
Methods………………………………………………………………………………………………………………………….. 10 – 11
Ethical Considerations……………………………………………………………………………………………………… 12 - 14
Results……………………………………………………………………………………………………………………………… 15 – 29
Discussion………………………………………………………………………………………………………………………… 30 - 33
Conclusions……………………………………………………………………………………………………………………… 34
Acknowledgments…………………………………………………………………………………………………………… 35
References……………………………………………………………………………………………………………………….. 36 - 37
APPENDIX 1: Topic Guide for in-depth interviews…………………………………………………………….. 38 - 40
APPENDIX 2: Participant Information Sheet……………………………………………………………………… 41 - 42
APPENDIX 3: Participant Consent Form…………………………………………………………………………….. 43 - 44
APPENDIX 4: Snapshots from the field..…………………………………………………………………………….. 44 - 47
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Study Details
Title:
Understanding the barriers experienced by the people of an urban slum in Bangalore to access the primary
diabetes and hypertension care facilitated by the Institute of Public Health (IPH)
Primary Investigator:
Anusha Purushotham
Supervisors:
Dr. Mrunalini Gowda (IPH), Dr. Rahul ASGR (SOCHARA), Dr. Narayanan Devadasan (IPH), Dr. Thriveni BS
(IPH) and Mr. Sabu KU (SOCHARA)
Name of the Field:
KG Halli, Bangalore, India
Duration:
August 2014 – October 2014
Affiliations:
Research report prepared as part of the Community Health Learning Program (CHLP) at SOCHARA (Society
for Community Health Awareness, Research and Action), Bangalore, India in collaboration with the
Institute of Public Health (IPH), Bangalore, India.
Funding Details and Budget:
The researcher was funded through the monthly stipend received in the Community Health Learning
Program (CHLP), SOCHARA. All travel costs to the field were covered using these funds.
Ethics Statement:
Research proposal was accepted and approved by the SOCHARA Institutional Scientific and Ethics
Committee in August 2014.
1
Background
The world is facing a recent epidemiological shift from communicable diseases to chronic noncommunicable diseases (NCDs), particularly diabetes and hypertension.In 2008, 36 million out of the 57
million deaths (53%) that occurred across the globe were caused due to NCDs and 80% of the NCD deaths
occurred in low and middle income countries (1). Out of the worldwide total of 970 million people with
hypertension and 382 million people suffering from diabetes, approximately 640 million hypertensive
patients (65.98%) and 305.6 million diabetic patients (80%) live in developing nations (2,3). Therefore, this
epidemiological trend is of particular interest in developing nations, especially India, where the disease
burden is consistently rising. The prevalence of hypertension in urban India is 25% and rural India is 1015% (4). With 65.1 million diabetics (prevalence 7.1%), India has the second highest number of people
with diabetes in the world (2). In urban south India prevalence of diabetes has risen from 5% in 1984 to
13.9% in 2000 (5).
This rise in the burden of chronic diseases has been complicated by another phenomenon, urbanization.
The rate of urbanization in India is proceeding at a very rapid pace with a quarter of the urban population
living in slum areas (6). The urban poor experience a very complex set of socio-economic, cultural, and
political barriers that lead to inequity in health care access (7, 8). Among all these reasons, even in the
general population, affordability is the second most common reason (first reason being people
considering the ailment not serious enough) for not seeking health care in India (9) and recent studies in
the Indian context have revealed that cost of care alone could be a driving factor to forego care altogether
among the poor (10). It is the second most frequently reported reason (after long waiting lines) that the
urban slum dwellers in India perceive as a barrier to health services (11).
Kadugodanahalli (KG Halli) is an urban neighbourhood classified as one of the 198 administrative units in
the city of Bangalore, the capital of the South Indian state of Karnataka. KG Halli has an area of 0.7 square
kilometers and a population of over 44,500 (12). It is a lower middle-class income area with over 75% of
the population earning less than $2 a day (INR 110) (8). A slum is generally an area where the urban poor
reside, typically characterized by poor living and sanitary conditions. In KG Halli, there are presently two
registered slums and one former slum, which was razed down in 2011 and replaced by a corporation
quarters with better housing facilities for the slum dwellers.
2
Figure 1: Map of KG Halli
(Ward 30)
KG Halli has been the site for the Urban Health Action Research Project (UHARP) of the Institute of Public
Health (IPH), Bangalore, since 2009. UHARP was launched with a mission to improve the quality of health
care of KG Halli residents by working with the community, the local health services (private and
government) and health authorities (13). Over the past five years the UHARP has been working with the
community to understand their needs with the help of trained Community Health Assistants (CHAs). CHAs
are trained by the UHARP team based on the ASHA modules, and they conduct regular house visits in the
community, disseminating information about basic health issues, nutrition, hygiene, immunization and
link people to the appropriate health services, under the supervision of UHARP staff when needed.
UHARP’s other activities include facilitating a dialogue between the various stakeholders in the
community to establish a common platform of health service provision, creating health awareness in the
form of school health programs/rallies and promoting youth empowerment by establishing a community
library and evening computer classes.
3
Figure 2: Community Health Assistant
(CHA) interacting with the community
Figure 3: CHA helping children with
their homework in the IPH
community library
Figure 4: Computer classes in the IPH
community center in KG Halli
4
An exhaustive census in the form of a house-to-house survey was conducted by UHARP in KG Halli
between June 2009 and March 2010 to understand the socio-economic status and health-seeking
behaviour of the urban community in the context of a pluralistic healthcare system. This self-reported
census data showed, among all diseases, a high prevalence (13.8%) of chronic conditions in the adult
population in KG Halli with 6.4% diabetes and 10% hypertension (16). KG Halli has a mixed healthcare
delivery system with 2 government and 32 private health care facilities, most of which are small clinics
run by general practitioners (GPs).
Figure 4: Community Health Center
(Government CHC)
Figure 5: A private clinic and an
adjacent pharmacy in KG Halli
5
69.6% of the surveyed households incurred high out-of-pocket (OOP) expenditures for chronic conditions
with 16% families facing financial catastrophe by spending more than 10% income on OOP (12). This
doubled the poverty rate every month (12). A subsequent study conducted in 2013 revealed that despite
the vicinity of abundant healthcare centers, one of the major barriers to care reported by diabetic patients
in KG Halli is financial hardship (8). The largest share of healthcare OOP has been on medicines, particularly
in chronic care where medication needs to be taken for a lifetime (14). Other reasons that drive up the
OOP are: the lack of medication and diagnostic services within government facilities, which forces patients
to visit different private facilities for different components of care (8). Hence, all these services need to
be integrated in one location in the public sector, the private healthcare sector costs should be regulated
and financial protection must be provided to patients against huge impoverishing OOP costs (8).
When details of the study were discussed with the community and health providers, both the stake
holders suggested that increasing the availability and accessibility of low-cost medicines would be the first
step in dealing with this issue. Several negotiations were conducted with both the private health providers
and the government facilities (CHC and UHC). However, the private health providers were reluctant to
prescribe low-cost generic medicines since pharmacies in the area either did not stock generics or sold
generics at the same price as brand medications. UHARP’s attempt to strengthen the existing government
facilities saw no success because the requisites recommended by the government health facilities were
not feasible for the project.
Therefore, the IPH Hypertension and Diabetes clinic (primary care clinic) was started by UHARP on January
6th 2014 as an experimental model to provide affordable, quality and patient-centric diabetes and
hypertension care to the residents of KG Halli. The clinic operates every Monday, between 2pm and 5pm
and offers free consultation and counseling services by trained medical doctors and nurses. The clinic also
dispenses generic diabetes/hypertension medicines at a subsidized rate. The clinic is equipped with a BP
monitor and finger-stick testing for random blood glucose monitoring. For the first three months, the
clinic was staffed by a doctor from a Christian mission hospital in the area while IPH was only involved in
procuring and dispensing medications. Presently, due to shortage of doctors from the mission hospitals,
two UHARP personnel, who are trained medical doctors, operate the clinic while the Christian mission
hospital continues to send nurses to the clinic.
6
Figure 6: IPH Diabetes
and Hypertension
Clinic
Figure 7: Doctor- patient
interaction in the clinic
Figure 8: Patient
counseling services
7
Among the slums in KG Halli, one particular slum, Slum A, was identified to be on the lowest rung of the
economic ladder, with residents unable to make ends meet (Snapshots of Slum A in Appendix 4).
Therefore, the UHARP team, along with the support from its funding agency, decided to offer free
medicines to the people of this particular slum in addition to the other free services at the IPH clinic. The
Community Health Assistants (CHAs) of UHARP who have worked closely with the community over the
past four years identified 22 residents (as of May 2013) in Slum A who have diabetes and hypertension.
The CHAs visited their houses, created awareness about the free services in the IPH clinic and gave “health
cards” that qualified them for free medicines and insulin in the IPH clinic. These cards have information
such as name of the patient, address, contact information and family member details.
Figure 9: IPH Health
Card and Patient Diary
Despite the expressed need by the community, awareness created by the CHAs in Slum A and the
utilization of the IPH clinic services by residents from various other areas of KG Halli, only 6 out of 22
diabetic/hypertension patients of Slum A have come to the IPH clinic as of August 2014. Even among these
6 patients who visited the IPH clinic, only 2 patients visited more than twice and none have returned since
March 2014. Currently, there are no patients from Slum A who are availing the services of the IPH clinic.
Therefore, there is a need for a systematic in-depth study to understand why the residents of Slum A,
despite being promised free medicines and treatment at the IPH clinic, are not availing these services.
Aim
8
This study aims to explore and understand the potential barriers experienced by the residents of Slum A
to access primary diabetes and hypertension care in the IPH clinic.
Objectives
•
To identify the socio-economic, cultural, physical, structural and political barriers that are unique
to residents of Slum A that prevent them from seeking diabetes and hypertension care in the IPH
clinic.
•
To understand the history of disease(s) in the diabetic and hypertensive residents of Slum A, their
health-seeking behaviour and healthcare expenditure.
•
To understand their perceptions regarding the quality of care at the IPH clinic and particularly
explore their attitudes regarding generic medicines dispensed in the clinic.
•
To list the learnings from the study that could benefit the UHARP team to modify the current
functioning of the IPH clinic and improve the accessibility of diabetes and hypertension care to
the residents of Slum A and KG Halli as a whole.
Methods
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Participants:
A qualitative approach using in-depth interviews was adopted for this study. The study population
comprised of people from Slum A who have diabetes and/or hypertension. The participants were
identified using the following inclusion criteria –
a) Must be a resident of Slum A.
b) Must have diabetes and/or hypertension (self-reported).
c) Must have the IPH Health Card prepared under their name.
An exhaustive sampling approach was adopted to obtain all the viewpoints of the problems since the
population size was small.
Materials and Procedure:
In-depth interviews were conducted in the households or any location within the neighbourhood of Slum
A that was convenient for the participants. Sixteen in-depth interviews were conducted. The first six
interviews were conducted by the Primary Investigator (PI) and one of the study supervisors. The next ten
interviews were conducted by the PI alone. In order to avoid unnecessary distractions to the participants,
the interviews were conducted in a relatively quiet location. Prior to the interview, verbal consent was
taken from the participant if they were comfortable having family members, neighbours or others present
during the interview. Apart from the participant, interviewer(s) and translator (CHA), all others were
instructed to not intervene during the interview unless they acted as a secondary source of information.
Informed consent was obtained from the family members who acted as a secondary source of
information. Interviews were carried out using one of the following local languages – Kannada, Tamil or
Urdu. A semi-structured interview format was followed using a topic guide (appendix 1). Prior to the
launch of the full study, three pilot interviews were conducted in a neighbouring slum – Slum B which is
also located in KG Halli and is comparable to Slum A. The final topic guide was evolved based on the
preliminary responses in the pilot. The PI conducted the interviews in Kannada and partly in Urdu.
Interviews in Tamil and Urdu were conducted with the assistance of a CHA who acted as a translator and
translated the interview between Kannada and Tamil/Urdu in situ. Details of the study were explained in
the language the participant could understand and the informed consent for participation was signed
prior to the interview. If the participant was illiterate, a thumb print was obtained in the presence of a
literate witness of the participant’s preference. With the consent of the participant, interviews were
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recorded using the SONY MP3 Digital Voice IC Recorder (Model: ICD-UX71F) owned by UHARP in KG Halli,
Bangalore. If the participant was uncomfortable with the audio-recording, the PI instead wrote down the
interview verbatim in a notebook after translating into English in situ. A soft-copy version of the English
transcript was then prepared post-interview. All audio-recordings of the interviews, on the other hand,
were translated from Kannada to English only after the interview and the soft-copy versions of the English
transcripts were simultaneously prepared.
The data was analyzed thematically using Atlas.ti software. First, all the transcripts were coded using
Atlast.ti and the preliminary codes were reworded/reviewed for any repetitions. Then, similar codes were
organized into categories. Several iterations of this categorization were done until the final themes were
recognized.
Ethical Considerations
11
Listed below are the four ethical principles for research and how the study addresses these principles –
1. The Principle of Non-Maleficence: The risks involved in this study were minimal and no harm to
the physical, mental and psychological health of the study participant or the community is
anticipated. The interviews were conducted in the comfort of the households or neighbourhoods
of the participants as per their preference and thus,no physical harm was expected. Researchers
were trained to conduct interviews with utmost respect to the participant’s emotional, mental
and psychological wellbeing so as to not cause any unnecessary harm or distress.
2. The Principle of Beneficence: This study was undertaken with the intention of understanding the
barriers to accessing free diabetes and hypertension care in the IPH clinic and in turn, proposing
measures to address these barriers to improve the clinic accessibilityto the Slum A community.
Although there were no direct monetary benefits from participating in the study, the information
participants provide will aid in future research and activities that will contribute to improving the
overall quality of care in their neighbourhood.
3. The Principle of Autonomy: Protecting the rights and dignity of the participants wasthe top
priority throughout the duration of the study. Participantshad complete autonomy over the
decision to participate in the study or withdraw their participation at any point during the study.
At the beginning of the study, participants were provided with a written informed consent and
details of the study were explained verbally in the local language. Even after the completion of
the study, at any time in the future, participants will have the right to revoke their consent to use
information obtained from them for present or future research purposes. Participants were
clearly informed that they are not required to provide any reasons for these decisions and none
of their decisions would jeopardize their relationship with IPH.
4. The Principle of Justice: All study participants were treated fairly and no discrimination was made
on the basis of gender, age, color, socio-economic status, religion, language, caste or creed. The
study protocol remained the same across the study population and no individuals or groups of
people received unfair treatment. The risks and benefits of the study will be equally distributed.
Additional details
12
Relationship with Participants: Participants were treated as indispensable partners in research and their
dignity was upheld at every stage of the study. Participants were chosen based on inclusion criteria that
did not unfairly exclude any group of people from participating or receiving benefits of the study.
Participation was completely voluntary and no methods of coercion or false promises were adopted to
ensure participation. Participants’ time was respected and the duration of interviews did not exceed than
what was necessary.
Informed Consent: Participants were provided with a written information sheet (appendix 2) detailing the
study purpose and objectives, and their rights as autonomous voluntary participants. Information on what
data will be collected, how it will be used and the risks/benefits of the study are also included. If the
participant was unable to read, the information sheet was read out to the participant. Informed consent
for participation in the interview, audio-recording and publishing the interview verbatim (appendix 3) was
obtained prior to the interview. If the participant was illiterate, a thumb print was obtained in lieu of the
signature in the presence of a witness who was of the participant’s choosing.
Confidentiality: Interviews were conducted in a location of the participant’s preference. To protect the
privacy of the participant, apart from the PI and CHA, only those family members, neighbours or others
identified by the participant were present during the interviews. Verbal consent was taken from the
participant to allow them to be present in the interview. Audio recordings were made using the SONY
MP3 Digital Voice IC Recorder (Model: ICD-UX71F) owned by UHARP in KG Halli. All audio-records were
securely stored and accessed only by the UHARP team for research purposes. In cases where the
interviewee declined to be audio-recorded, the hand-written interview transcripts were securely stored
and access was restricted to the UHARP staff. At all times during the project, confidential data was handled
only by the PI and the UHARP team. If the study results are published, any information that identifies the
participants will not be made public. If the participant chooses not to have their words published verbatim
(option provided in informed consent), measures will be adopted to refrain from quoting the participant
in any publications. The participants retain their right to view at any time the information that is collected
from them and the right to deny usage of their details.
Serious Adverse Events: While risks involved in this study are minimal, the only possible adverse event
that could possibly occur is the breach of confidentiality of the study participant. Protecting the identity
of the participants was of utmost priority during the entire study period and after. If any instance of
violation of confidentiality is brought to the PI’s attention, the PI will consult with the supervisors and
potential actions for recourse will be implemented immediately.
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Indemnity Issues:
No monetary compensation was provided to the participants for partaking in the study. The study involves
in-depth interviews conducted in the homes or neighbourhood of the participants. Due to the nature of
the study, no physical risks were expected. Therefore, there was no necessity for insurance to compensate
the participants.
Statement of Conflict of Interest:
There are no conflicts of interest to the best of the researchers’ knowledge. The researchers agree to
comply with the relevant national and applicable international guidelines. The PI was not involved in any
ongoing projects during the study period.
Results
The details of the sixteen interview participants are mentioned in Table 1. For the column titled “Attended
IPH clinic” the number in parenthesis indicates the number of times the people have attended the clinic.
Out of the 22 people identified by the CHAs to be eligible for the IPH health card, 6 were not included in
the study for the following reasons –
14
•
•
•
1 resident was not available for interview
2 residents were deceased
3 residents were wrongly identified as having diabetes or hypertension
The in-depth interviews were used to first understand issues related to the history of the disease, healthseeking behaviour and health expenditure of the participants in order to set up the context before
exploring the constraints residents of Slum A faced in accessing the IPH clinic.
History of disease and health-seeking behavior
All the 16 participants interviewed had been diagnosed with either diabetes or hypertension for at least
1 year. The duration of disease ranged from 1.5 – 20 years with 4 participants having the disease for more
than 10 years. All but 2 participants reported symptomatic disease detection i.e. they were diagnosed
with the disease only after they experienced symptoms.
“First I had dizziness and they took me to a private hospital. There they told me I had BP. There they gave
me tablets for BP. I took BP tablets for 4-5 years. It was normal after that. Suddenly I had problems with
my eyes and they took me to Bowring hospital. There they told me I had BP and sugar.” [P5, female 77
years]
There was mix of healthcare facilities where the disease was first detected – participants went to both
government and private clinics when they were first diagnosed. However, very few participants chose to
continue treatment at government facilities and instead switched over to private providers either due to
their own experiences at government hospitals or due to reviews they heard about private providers
from others.
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Table 1: Details of the interview participants
Particip Age Sex
ant No. (yrs)
Diseases
Duration of Interviewer
disease
(yrs)
Language
interview
of Religion
Occupation
Attended
IPH Clinic
P1
45
F
DM
15-20
AP and MG
Kannada
Hindu
None
Y (2)
P2
43
F
DM
6
AP andMG
Urdu
Muslim
Beedi-maker
Y (1)
P3
55
F
DM and HTN 15
AP andMG
Urdu
Muslim
None
Y(4)
P4
56
F
HTN and DM 5
AP andMG
Kannada
Christian
Rag-picker
N
P5
77
F
HTN and DM 2 (DM) 5 AP andMG
(HTN)
Urdu
Muslim
None
N
P6
50
M
DM
2-3
AP andMG
Urdu
Muslim
Faith-healer
N
P7
55
M
DM
3
AP
Kannada (primary) Hindu
Tamil (secondary)
Construction
worker
Y (1)
P8
60
F
DM and HTN 1.5
(both under
control)
AP
Kannada
Christian
Hospital cleaning Y(2)
staff
P9
59
F
DM and HTN 2
(HTN under
control)
AP
Urdu
Muslim
None
N
P10
50
F
HTN
6
AP
Urdu
Muslim
Clinic
staff
cleaning N
P11
48
F
HTN
16
AP
Kannada
Hindu
Beedi-maker
P12
42
F
HTN
7
AP
Kannada(primary)
Tamil (secondary)
Hindu
Office
staff
P13
38
M
DM
8
AP
Kannada
Hindu
Domestic worker N
P14
70
M
HTN
20
AP
Urdu
Muslim
None
P15
70
F
HTN
4-5
AP
Urdu
Muslim
None (begs alms) N
P16
55
F
DM and HTN 5
AP
Urdu
Muslim
None
N
cleaning N
N
Y (2)
DM – Diabetes Mellitus, HTN – Hypertension, AP – AnushaPurushotham, MG – Mrunalini Gowda
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Following their diagnosis, participants exhibited diverse health-seeking behaviours. Some took
medications daily and visited their doctors for regular checkups (once in 1-3 months) but most saw their
doctors only when they experienced severe symptoms. Adherence to medications depended on many
factors, predominantly the availability of money to buy medicines or the presence of symptoms. Such
patients chose to either alter the dose of medication or completely stop taking medications on their own
without consulting a doctor. Some missed taking medications at times because of forgetfulness.
“1-2 days I miss until they give me money for the tablets.” [P16, female 55 years]
“When he gets dizzy, he eats. When he does not get dizzy, he won’t eat.” [daughter-in-law of P14, male 70
years]
Another interesting theme that emerged was many people reported that they had little awareness about
the disease when they were first diagnosed and thus, neglected taking medicines properly. Once their
symptoms became severe, they realized the consequences of not complying with treatment and later
started taking medicines regularly.
“I took tablets. I did not know much about the tablets that time. I did not know what problems could arise.
Very carelessly I stopped. I used to take it when they gave the tablets and then stop. Only after I started
having problems, I took some care and started taking insulin.”(P13, male 38 years)
Healthcare expenditure
Patients spent approximately between Rs.100 and Rs. 500 per month for diabetes or hypertension
medications alone, with the highest expenditure being Rs.2000 per month. Only 2 of the 16 participants
were using free medicines from the government. In addition to medications, patients spent between Rs.
70 and Rs. 500 for doctor’s fees and lab tests. Some patients reported that their family doctors sometimes
waived consultation fees or lab fees in consideration of their financial difficulties.
“Sometimes they take Rs.50 also from me. They know us, poor people. He doesn’t take from us.” [P2,
female 43 years]
People had several ways for bearing their healthcare expenses, the most common being financial support
from their family members. The second most common source of payment was through their earnings.
Since most participants worked in the unorganized labour sector and earned daily wages depending on
17
the availability of work, this income flow was variable. The last source of finances people resorted to was
borrowing loans, especially during episodes of hospitalization when huge expenses were incurred.
“What to do, my kids give me and I take it. I have 3 sons. If they give me, then it will be enough for our
spending.”[P6, male 50 years]
“I go to the clinic for work, right? They give me 500 rupees per month. I use that for tablets and all.” [P10,
female 50 years]
“I beg for alms in the masjid. I don’t have anyone to take care of me.” [P15, female 70 years]
“We had to take loans from here and there. We have to. What else to do?” [Wife of P7, male 55 years]
Most people expressed that the financial burden of their diabetes or hypertension care placed a huge
strain on themselves and their families. With this understanding of the residents of Slum A, the interviews
proceeded further to explore the constraints they experienced in accessing the IPH clinic that provided
them with free primary diabetes and hypertension care.
Barriers to accessing the IPH clinic
The findings that emerged from the analysis of the 16 in-depth interviews in exploring the barriers to
accessing the IPH clinic have been divided into 7 main themes. Relevant sub-themes under these main
themes are also included.
1. Inadequate awareness about IPH clinic
Patient does not know anything about the clinic
Lack of awareness about the IPH clinic was a significant theme that emerged during the interviews. When
asked about the clinic, patients were either completely unaware of the clinic or they had partial/wrong
information about the clinic. Out of the 16 people we interviewed, 4 people reported having absolutely
no knowledge about the IPH clinic. It was the first time that they had even heard of the clinic or that it
provided free medicines/services. 3 of these 4 were not given IPH health cards and thus, this could be the
most probable reason for their lack of awareness about the clinic.
“No, I did not know. I found out just now.” (P13, male 38 years)
Patient does not know where the clinic is located or does not know the timings of the clinic.
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People, who had heard about the clinic and had the card, did not know where it was located. They were
confused about the location of the clinic or stated other primary reasons that prevented them from taking
the effort to know about the location of the clinic. Some people also were unsure about the timings of the
clinic.
“I came twice to the address you told me and I looked there. I did not find the clinic, so I went again to
Bowring.” (P5, female 77 years)
“She told me and gave me the card and all. I myself have not gone. I didn’t get time and didn’t know how
to go there.” (P12, female 42 years)
Patient confused about IPH clinic and other organizations
There are several NGOs that work in Slum A on health and other related issues. Hence, people tended to
confuse IPH with these other organizations. Due to the proximity of the government Community Health
Center (CHC), which is located less than a kilometer away from the IPH clinic, some patients also confused
the IPH clinic with the CHC.
“No, my daughter went there for delivery. Also took the kids for checkup. Near the police station. They
check the weight of the kids.” (Participant talking about the CHC when asked about what she knows about
the IPH clinic) [P10, female 50 years]
2. Inadequate follow-up/misidentification of patients by Community Health Assistants (CHAs)
Timings of the CHAs not matching with the availability of patients
Lack of communication between the CHAs and some sections of the community was a critical barrier that
emerged during analysis of the interviews. Mismatch in the work timings of the CHAs and the people
proved to be a major reason for this inadequate communication. The CHAs visited the community
between 10am and 5pm on weekdays and therefore, missed out on interacting with many people who
went out for work during the day.
“They [pointing to CHA] also come and when they come to check, I am not there. That is the problem.”
[P11, female 48 years]
No health card given to some patients
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6 out of the 22 identified patients were not given the IPH health cards primarily due to the reasons
mentioned above. Although the cards were printed with their names, they were not distributed to the
patients. Among the 6 patients with no cards, 1 reported partial awareness about the clinic since the CHAs
spoke to her while surveying the area, 1 patient was deceased and 1 patient was not available for the
interview. The remaining 3 patients said they had no knowledge about the clinic. These were the same
patients mentioned in the theme titled “Patient does not know anything about the clinic.”
Interviewer: “Did you get a card? [Pointing to a IPH health card that we had] Like this, did someone give
you a card?”
[P10, female 50 years]: “No, no. No one gave.”
Lack of follow-up by CHAs
Although a majority of the people mentioned that they recognized the CHAs and that they visited them
many times, few people reported rarely seeing or interacting with the CHAs.
Interviewer: “You did not find the clinic. Did you tell anyone among the three of them (CHAs) that you did
not find the clinic?”
(P5, female 77 years): “No, no one came.”
Wrong identification of patients
3 of the 22 patients were wrongly identified as having the disease (DM and/or HTN). This was due to the
inadequate understanding of the disease symptoms by both the patients and the CHAs.
3. Perception of medications
The 6 participants who had been to the IPH clinic at least once had a general positive opinion about the
clinic and the staff. Most of them recounted that they were counseled about their disease and information
was given about self-care, exercise and diet. They also said that the doctors and nurses were friendly.
Overall, when asked about their experience in the clinic, people mostly said “good.”
“The doctors come and check sugar and BP. They tell this and that. They tell that it will become better…
Yes, the computer is there no. In that they told me to see. They show for 15-20 mins and I have seen it…
20
“You have the disease. Do this, be proper and take care of yourself. Take care of your health,” it says all of
this.” [P15, female 70 years]
However, when probed further, people felt that although the clinic was “good”, they had a problem with
the medicines dispensed. Perception of the generic medications dispensed in the IPH clinic was one of the
major reasons that people cited for not accessing the clinic. People formed different opinions about the
medicines either through their own experience of consuming the medicines or were influenced by others.
“It (IPH clinic) was good. There were a lot of people. I thought, “Let me go see.” So I went there. When the
(private) doctor told me that the medicine did not suit me, “Don’t eat this, ma, this other medicine. Use
whatever you used before.” I stopped taking it and I am using this only.”[P1, female 45 years]
Experiencing side-effects
Of the 6 patients that came to the IPH clinic, 2 patients reported side-effects from the medicines. Patients
reported taking the medicines for at least one month before they started experiencing side effects and
felt that their disease was not under control.
“I took for one month. Nothing happened. I took the next month. After eating, BP and diabetes both
became high. I became weak – hands and legs. ……There was burning here. And then the whole feet. I put
on vicks, I put on iodex. I put on a turmeric cloth. Afterwards, with iodex it became less. The pain.”[P3,
female 55 years]
Family doctor’s perception about the effectiveness of the medicines
When patients showed IPH medicines to their family doctors, the doctors informed them the medicines
were ineffective and they needed to revert back to their old medicines. The trust in their family doctor’s
opinion influenced patients to stop coming to the IPH clinic.
“I went to [Private] Clinic and they said, “Power is less in these tablets. You take this only. That does not
suit you.” [P3, female 55 years]
Poor quality of medicines
21
One patient reported that the medicine became powdery when she tried to open it. She complained of
no side-effects, however. The patient insisted that this was the main reason for not coming to the clinic
and she would come if the clinic gave “good medicines.”
“No pain or anything.That medicine, it would become just like a powder. Like a powder. When I ate, I didn’t
feel right…. If you give good medicines, I will come.” [P16, female 55 years]
Experience of neighbours
One person in the community fell ill and was hospitalized. Word spread in the community that the IPH
medicine was the cause of this incident. People began discussing among themselves about the
experiences they had or heard from others about IPH medicines and came to the conclusion that the
medicines were not suitable for anyone.
“They all ate no. It became more for all of them. That old lady was admitted for 5 days in the hospital.
Then I thought we don’t have money with us right now to get admitted. All our money went away. We
don’t have anything. We earn money and eat. That is why I didn’t eat any tablets because I was scared.”
[P2, female 43 years]
Fear of changing to a new healthcare facility or medication
Among the people who had heard about the IPH clinic but had never been to the clinic, their preference
and trust in their current healthcare provider far outweighed the monetary benefits of trying a new free
clinic. People went on to say that they would only come to the IPH clinic if they received the same brand
of medicines that they are currently taking.
“My mind tells me, “Don’t take any other medicines. Continue this tablet only.” That is why I take this
only… I have been going since 20-30 years to [Private] clinic. That is why I will not take it anywhere else. If
I eat anything else, after eating my face becomes like this [puffs up her cheeks]” [P15, female 70 years]
“If you give us tablets, I will come. If you give us our tablets, we will come.” [P2, female 43 years]
Mistrust in government health facilities and confusion about IPH clinic as a government facility.
22
Most people expressed mistrust in government facilities either based on their own experiences or
experience of others. Due to the inadequate awareness about IPH clinic and the perception in people’s
minds that “free medicine” is synonymous with “government medicine,” people were skeptical that the
clinic dispenses poor quality “government medicines.” Therefore, they refrained from coming to the clinic
altogether.
“…thinking that government tablets don’t suit me either, even I didn’t eat. I never take government tablets.
My stomach starts burning and my health gets bad….. The old lady said that “It is free, government
medicines.””[P2, female 43 years]
4. Distance
Unable to walk the distance to the clinic and afford extra cost of travel
Distance was a physical barrier that people reported in accessing the clinic. The clinic is located about <2
kms away from the neighbourhood and while some felt that this was within walking distance, many said
that they need to take the bus or the auto to come to the clinic. Most of the diabetic patients complained
of pain in their feet which made it even harder for them to walk the distance to come to the clinic. People
who felt that the clinic was too far cited the extra money for traveling was a constraint from coming to
the clinic.
“I came back and told her [looking at the CHA] that “I am not coming. I can’t go that far. If I go walking
then my feet hurt. My feet hurt all night.”[P3, female 55 years]
“I will come to get the tablets if you can help with the travel to and from there.”[P14, male 70 years]
Other health facilities are closer
Due to the abundance of many private clinics in the vicinity that had established trust with the community,
some people preferred continuing to seek care in those clinics as they found the location of the IPH clinic
inconvenient.
“I go walking. It is close by. Behind.”(when talking about her current clinic)[P3, female 55 years]
5. Restricted Timings
23
Clinic timings conflicting with work timings
In addition to the distance, timing of the clinic was an important limiting factor that decreased the
accessibility. The clinic is open only on Mondays, between 2pm and 5pm. This restrictive timing prevented
people who go to work during the day from accessing the clinic. Majority of the patient population who
work were daily wage labourers and hence, taking even a day off amounts to the loss of a day’s pay.
“The timing doesn’t match. If I don’t go to work for a day, they cut the wages. That is why. There if my
wages get cut..” (P12, female 42 years)
Other health facilities with more convenient timings
Other private health facilities in the area were open for longer hours - during the evenings and sometimes,
even on weekends. This made it convenient for people to access the clinic after work and thus, they
preferred these clinics over IPH clinic.
Interviewer: “What time do you go to [private] clinic?”
[P11, female 48 years]: “I go in the evening, amma…. I have not gone (to IPH clinic) because I don’t have
time, that’s all.”
6. Health-seeking behaviour
Attitude about own disease
The past health-seeking behavior of the respondents gives some insight into why they decided against
coming to the IPH clinic. Many people felt that they needed to go to the doctor only when they had
symptoms and there were long periods of time (6months – 3 years) when they would not see any doctor.
Some of them did not have a preference for any particular doctor and would seek treatment at any facility
that was convenient at the time of illness. Therefore, since such patients had not experienced any severe
symptoms recently and did not feel the need to go to a doctor, they might not have come to the IPH clinic.
“I go anywhere and everywhere…. I have it (tablets), I buy that and eat…..If I get fever, cold or body aches,
I would go. If not, I would not go.” [P12, female 42 years]
24
Among the others who exhibited irregular health-seeking behaviors, some had accepted that death was
inevitable, so they did not feel the need to comply with their doctor’s instructions or take medications
regularly.
“Anyway, one day we all should die, so leave it” thinking that I stopped (taking tablets).” [P7, male 55
years]
Among the 16 participants, only 1 mentioned that her diabetes and hypertension were currently under
control and since she was told by several doctors that she did not need any medications, she stopped
coming to the IPH clinic. This patient showed a high level of understanding about the disease and strictly
adhered to the treatment regimen and diet. She continues to get her sugar and BP levels monitored
monthly.
“After I got diabetes I became very scared. After that I went to so many places and got my blood checked,
do you know? Any place people told me I went. Even when they say pay Rs.50 and get it checked, I would.
The reason being, in (private) hospital I see, right? Hand amputation, leg amputation and all that! That is
why I used to get it checked regularly. I was afraid. That is why now I don’t have anything. It is normal.”
[P8, female 60 years]
Source of payment of health expenditure
Some patients said that the only reason that they were able to afford the cost of the medications and
treatment in private clinics was because they were receiving financial assistance from their family
members or from their place of work. If they did not receive this support, they would have come to the
IPH clinic for the free medicines.
“I don’t pay. The people whom I work for, they pay... They give me money and I buy it. Fees whenever I go
to the doctor I only pay 100 rupees. For tablets they give…
[Speaking about what she will do if her employer doesn’t pay for medicines]
I have to pay or my kids have to. Otherwise I have to go to this [IPH] clinic. That is what. I am talking about
it openly. If they did not give me, my kids get salary every month otherwise I have to go to this clinic. To
them only [pointing at the CHA].”[P11, female 48 years]
25
Alcoholism
One of the respondents reported that his habit of drinking alcohol was the main reason that prevents him
from coming back to the IPH clinic. Although he did not admit it himself at first, after much discussion, his
wife informed us that he is afraid to take diabetes medication while drinking alcohol as he is aware of the
ill-effects of mixing the two. Despite being hospitalized twice due to complications from diabetes, he
chooses to not comply with the treatment.
P7’s wife: “If he takes the medicine, he won’t be able to drink liquor. So that is why he stops.”
[P7, male 55 years]: “Yeah, that is the reason. Nothing else.”
The wife went on to tell us the various measures, including faith healing that they have taken to stop his
alcoholism in vain. The entire family, including the children, has supported him to rid himself of the habit
and convinced him to take care of his health.
“We have tried so much, madam. He promises on all of us. He even promises to God. When he goes to the
hospital what he tells, “From today onwards I won’t drink. There are a lot of difficulties at home.” He thinks
about all of this when he is on the hospital bed. When he comes back home, he goes back to it. What to
do? That is why we don’t send him to work, we ask him stay at home itself. If he goes out for work and
earns money, he will drink. That is why we don’t send him.” [P7’s wife]
The patient on the contrary feels like he can stop drinking whenever he wants if he makes up his mind.
He states that he has stopped drinking in the past for as long as 6 months when he was hospitalized.
Therefore, he can stop anytime and come to the clinic.
“I don’t have anything like that, madam. For everything it is my mind that is the reason. If I want to stop
then I can stop, I am like that…. When I take medicines, I will be afraid that I can’t drink, right. If I stop
taking meds only then I drink. If I take meds, I can’t drink right.”
Despite the patient’s confidence, his wife felt less assured about the promise because the patient had
been recently discharged from the hospital but had already returned to his drinking. His alcoholism was
deeply rooted and she felt they needed more assistance to tackle the problem effectively.
7. Family Structure
Family dynamics also played an important role in the decision-making of the patients when it came to
choosing their health-care facilities. Majority of the patients said that they had very supportive families
26
who gave them complete autonomy over any decisions they made regarding their health. Their families
did not influence them to choose one health care facility over the other or discourage them from going to
the IPH clinic. However, there were other subtle familial factors that indirectly became barriers to
accessing the clinic.
Need someone to accompany to the clinic
This was a significant theme that emerged among the elderly patients we interviewed. Older patients
depended on family members to take them to the clinic and if no one was available to accompany them,
they would not be able to go anywhere. If the clinic was too far, they would instead prefer a closer clinic
so that it would be more convenient for their family members. Thus, these patients did not have complete
independence to choose when and where they wanted to go for treatment.
“I have pain in my feet, so I can’t go anywhere. Also, my grand-daughter is too young to take me to the
clinic. My daughter stays at home with her 5 children and she cannot take me. My son goes to work and
my daughter-in-law also has 5 kids. I went in auto 2-3 times to the clinic with 2-3 people. Because they
stopped, I also stopped going. That is why I stay at home itself.”[P16, female 55 years]
Lack of communication between family members
When the CHAs distributed the IPH health cards, some cards were given to the patients’ family members
and not directly to the patients (if they were unavailable or at work). This sometimes resulted in the
message not being conveyed to the patients because of the lack of communication within the family and
thus, the patient had little or no awareness about the IPH clinic.
“No, she (wife) did not tell me. She has her own tension at work. In the morning she has to take care of the
kids. I only come at 9-9:30 at night. I eat dinner and sleep. That’s all.” [P13, male 38 years]
27
Figure 10- Schematic diagram representing the major themes of why people are not accessing the IPH
clinic: Thematic analysis of the 16 in-depth interviews showed seven main barriers that prevent people
from accessing the IPH clinic. The major themes are represented in yellow and the sub-themes under
each major theme are represented in green.
28
Figure 11 - Pathways elucidating why people from Slum A are not coming to the IPH Clinic: This diagram captures the various pathways from the
starting point – IPH health card is prepared to final point – Patient does not come to the IPH clinic. These are tentative pathways that explain why
people from Slum A who were identified to have diabetes and/or hypertension are not coming to the IPH clinic. The two main scenarios are that the
patient either receives the IPH health card or does not receive the health card. Based on these two situations, different pathways can be traced. The
seven major themes – lack of awareness about the clinic, inadequate follow-up by the CHAs, negative perception of the IPH medicines, timings, distance,
health-seeking behaviour and family structure are highlighted. This diagram illustrates that the 7 themes are not acting in isolation but are interlinked.
29
Discussion
With the intention of addressing the financial burden of medications and thereby increasing compliance
and continuity of treatment in diabetes and hypertensive patients, IPH set up a clinic in January 2014.
Despite their eligibility to receive free medicines and treatment, the residents of Slum A reported several
constraints that prevented them from coming to the clinic. This study describes these barriers: lack of
awareness about the IPH clinic, inadequate follow-up/misidentification by CHAs, perception of IPH
medications, distance, restricted timings, health-seeking behaviour and family structure.
Lack of awareness about the IPH clinic was one of the major themes that emerged in the study. This goes
hand-in-hand with the next barrier - inadequate communication between the CHAs and the community.
Some patients said that they did not know specific details like timings/location of the clinic while others
stated they had never heard of the clinic. In order to further understand this implementation gap,
informal discussions were conducted with the three CHAs who worked in Slum A. All three CHAs (including
a fourth one who is no longer with IPH) had surveyed Slum A in September 2013 to identify the diabetes
and hypertensive patients in the area but only 2 of the CHAs went in January 2014, just before the opening
of the clinic, to distribute the health cards. Some houses were missed since they were locked during the
survey and/or card distribution. The CHAs reported that these houses belonged to daily wage labourers
who worked during the day. Although they went back again 2-3 times to the same houses, even during
the weekends, they were still locked. Therefore, 6 patients who were identified during the survey were
not given health cards because the CHAs only went to Slum A during the daytime. These patients with no
cards mentioned that had they been aware, they would have come to the clinic to receive the free
medicines.
A possible suggestion to tackle this problem of mismatched timings between the CHAs and the community
would be for the UHARP team to consider modifying the work timings of the CHAs such that they can visit
Slum A in the evenings for few days a month so as to reach out to this section of Slum A. This could also
address the issue of lack of awareness about the IPH clinic and inadequate follow-up by CHAs since the
CHAs would have more opportunities to periodically interact with the all/or most of the patients from
Slum A in the evenings, receive their feedback and listen to their concerns.
During the study, it was also discovered that 3 patients were wrongly identified by the CHAs to have the
disease(s). The CHAs stated that when they conducted the survey, patients who reported that they had
the disease(s) gave a different answer when they were interviewed for this study. Upon further probing,
we attributed this oversight to the lack of understanding of disease identifiers by the CHAs and patient
confusion about their own disease. Therefore, there is a need for further training and monitoring of the
CHAs so that they are able to spend more time with patients and have better knowledge about the specific
questions they need to ask before identifying patients.
Perception of IPH medications was another significant constraint. Experiences of neighbours or personal
experiences of side-effects from IPH medications made a huge impact in people’s minds and thus, patients
30
refrained from taking IPH medicines. Further investigation is needed on this topic to understand why
these patients experienced unpleasant symptoms, if these symptoms are truly side-effects of the generic
medicines and what the quality of the generic medicines was in comparison to their branded counterparts.
A possible explanation, if the side-effects are confirmed to be true, is that the generic drugs may have
inactive ingredients that are not suitable for these particular patients (17).
The poor opinion of other general practitioners’ in the locality regarding the effectiveness of generic
medicines dispensed in the IPH clinic played a huge role in influencing patients’ perception about the
medications. Informal discussions with the CHAs revealed that these physicians were usually linked to
local pharmacies that sold only branded medications and thereby, generic medicines were not preferred
by either the pharmacists or the physicians. This finding is consistent with another study conducted in
South India, which showed that community pharmacists and drug retailers had negative perceptions of
generics either due to low understanding about generics or preference to dispense branded medicines
that met the largest profit or incentive payments (18). The attitude of these professionals proves to be a
critical barrier to generic drug usage and calls for effective policies at a state or national level to tackle this
issue and promote the use of affordable rational therapeutics. At the community level, innovative efforts
can be re-initiated with health practitioners to support the use of generic drugs.
Most people who never came to the clinic confused IPH medications with “government medicines.” They
had pre-conceived notions that “free medicines” were “government medicines” and thereby, were of
“poor quality” and did “not suit them.” The CHAs too recognized this issue during their field visits and
stated that patients do not value the medicines because they are given free of cost. Patients have told
them repeatedly that they are willing to come to the IPH clinic only if they are given branded medicines.
None of the patients identified these medicines as “generic” and this could be possibly due to the lack of
knowledge regarding generics. Among those we interviewed, only two patients and their family members
felt that “government” and “private” medicines were equally effective.
Some of the older patients were afraid of switching over from a known drug that they had been using for
several years to an unknown drug. All these patients, despite their financial difficulties, were willing to
spend money and buy what they called “good” medicines instead of risking eating other medicines. When
asked how we could help, they asked that we provide them with either these “good” medicines or give
them money to buy those medicines. Therefore, this suggests a pressing need to remove the stigma
around government/generic medicines and create more awareness and trust among people regarding
their benefits. There are very few studies in the Indian context that explore patient’s perception of generic
medicines (17) and the findings presented in this study from a patient’s perspective is an important
contribution to this growing database of knowledge.
The work timings of many people conflicted with the clinic timings (Monday 2pm – 5pm). Since taking a
day off to come to the clinic would mean the loss of a day’s pay, accessing the clinic was out of question
for such patients. These patients requested that the clinic be open past 5pm, like the other private clinics
in the locality. Previous studies also show that limited opening hours is an important barrier in accessing
health services (19). Therefore, this problem could be addressed by opening clinics in the evenings to
accommodate more patients.
31
Distance of the clinic was another constraint that was mentioned, particularly by the older diabetic
patients. A common complaint they had was that the pain in their feet restricted their daily activities
including walking and therefore, they could not walk to the clinic on their own. They had to rely on family
members to come to the clinic. Some patients said they had to use an auto/bus and this extra expense of
traveling was a concern. Instead, they preferred going to clinics that are closer to their homes. CHAs
reported that patients had asked if they could bring medications to their houses instead. This is a possible
option that could be explored to make the free medicines more accessible to the elderly.
The role of family dynamics was also explored in the study. Many elderly patients were dependent on
their family members for financial support and also needed them to physically accompany them to
healthcare facilities as mentioned earlier. This limited their decision making power with regards to their
own health. Some elderly patients had no family support or government welfare options (pension cards),
and thus relied on begging for alms. Extra attention could be given to such patients and address their
unique needs like helping them with getting pension cards or travel assistance.
The complex health-seeking behaviour of patients is also critical in understanding why they chose not to
come to the IPH clinic. Some patients felt that since death was unavoidable, health was not priority for
them. CHAs too expressed similar accounts of their interactions with patients who preferred spending
money on eating meat rather than spending on medicines. These patients did not have any problems
specific to the IPH clinic, but had a general attitude that prevented/restricted them from going to any
healthcare facility regularly. Certain habits like alcoholism were also explored in this study and
necessitates the need to look into such behaviours.
It is important to note that the 7 themes identified in the study are not working in isolation, but are interrelated as represented in Figure 11. Various factors come together and act in different pathways to
produce the final effect: preventing residents of Slum A from accessing the IPH clinic.
In addition to the seven themes that emerged from the interviews, there are other issues that came to
light during the study. There are several organizations that work in Slum A on several aspects including
health and livelihood and unfortunately, people have been subjected several ethically questionable
practices. People have been recruited for clinical trials without their complete knowledge and sometimes,
organizations also make false promises that they ultimately don’t deliver. One of the CHAs who has
worked in Slum A for the past 4 years also described several instances where institutions bring their
students to conduct studies/surveys in the community for a short period of time and disappear without
any follow-up activities that benefit the people. This has also been recognized in an earlier study
conducted in KG Halli by IPH in 2013 (8). Despite the rapport and trust the CHAs have established with the
community in Slum A, these past experiences have understandably left some people in Slum A very
skeptical about the motives of any organization that works in the area. Therefore, stronger positive
relationships need to be established with the community and the UHARP team. Measures can also be
adopted to collaborate with some of the trustworthy organizations (NGOs) that work in the area and
create a more amiable environment for both the people and the organizations.
32
In order to gain a better insight about what the community wanted and expected, participants were asked
about how IPH could help them. While many people spoke about health-related issues like free medicines
or medical attention for other diseases, some requested help for the elderly, getting ration cards and
pension cards, help with the education of disabled children and monetary assistance. This threw light on
other concerns the community had that were not related specifically to diabetes and hypertension. Since
people felt like these issues were significant enough to mention in their interviews, it could allude to the
possibility that people considered these problems to be of high priority. This was consistent with the
conclusion of the informal discussions we conducted with the CHAs - the community had other more
pressing needs than diabetes and hypertension. Thus, if the UHARP team is able to address these concerns
effectively and in turn help with their overall well-being, trust will be built in the community about IPH
and they will take more interest in the health promotion activities conducted by CHAs and access the
clinic.
Another important learning from the study is that some people spoke about many health issues that they
or their family members faced. Therefore, if the clinic is able to provide overall primary health care in
addition to diabetes and hypertension, patients might be willing to come to the clinic as it would be a onestop shop for all their basic healthcare needs. An alternate option would be to re-instate efforts to
strengthen the existing CHC and UHC as a first-step, make generic medicines (particularly diabetes and
hypertension medications) available in the CHC/UHC to meet the demands of the patient population and
introduce counseling services in partnership with the Christian mission hospital. The CHC/UHC can then
take over both the tasks of procuring medications and provide counseling services when they see the
benefit of such services to the patient population.
The overall objective of the study was to understand the barriers faced by residents of Slum A from a
socio-economic, cultural and political perspective. During the initial interviews, we did not get a sense of
any political constraints that people felt in accessing the clinic. Perhaps, repeated interactions with the
people by the PI would have increased the comfort level of the participants and this might have helped
them talk about any political reservations they had about the clinic. Another study limitation was that the
participants were interviewed in the presence of a CHA from IPH who acted as a translator. This might
have affected the response of those patients who recognized the CHA and could have influenced them to
speak about the clinic in a more positive light. It also needs to be acknowledged that few interviews were
of relatively shorter duration (15 mins) due to either the participants’ busy schedule or in the case of some
elderly patients, their inability to concentrate for longer periods of time. This might have compromised
the results to a small extent. Due to the small scale of the study, the results may not be applicable to the
general population of the urban poor in India.
33
Conclusions
This study shows that despite the availability of free medicines and primary diabetes and hypertension
care facilitated by the IPH, residents of Slum A experienced several barriers to access the clinic. This
experimental model in providing free healthcare for NCD (diabetes and hypertension only) patients
revealed many critical factors that need to be considered before implementing a similar program in the
future. The foremost learning is that extensive awareness about the particular program must be created
and the program must be designed such that it addresses the community needs. Due to the complex
environment in Slum A created by some organizations, more efforts are needed to establish a positive
trusting relationship between the community and the UHARP team so that the community can express
their interests freely to the UHARP team and they can work together to meet the needs. CHAs need
further training and supportive supervision so that they are able to reach out to all sections of the
community. Structural barriers like timings and transportation should be accounted for.
This study demonstrates the important role of family support and extra assistance needed for the
especially vulnerable elderly patient population. It also shows that perception of generic medicines and
attitude about one’s own health are crucial factors in utilization of health services. Therefore, this calls for
extensive efforts from all sectors (private and public) to change the mindset of not only the patient
population but also the healthcare providers.
34
Acknowledgments
I would like to first thank the participants for welcoming me to their homes and sharing their stories with
me. This study would not have been possible without the cooperation of the participants, their families
and the Community Health Assistants (CHAs) of IPH – Mrs. Nagarathna, Mrs. Leelavathi and Mrs.
Tabassum. I would like to specially thank Mrs. Nagarathna, who accompanied me to the field every day,
including weekends, helped me translate the interviews and gave me crucial insights into the community
dynamics.
I would like to extend my gratitude to my supervisors at IPH, Dr. Narayanan Devadasan and Dr. Thriveni
BS, for giving me an opportunity to learn from their diverse public health experience. I am especially
thankful to the research coordinator of the Urban Health team, Dr. Mrunalini Gowda, who helped me at
every step of the way. She spent hours helping me trouble shoot unexpected problems that occurred
along the way – both on the field and behind the desk. Her constant support and encouragement was
integral to this project.
I would like to thank Ms. Maya Anne Elias (IPH) for her guidance with the analysis of qualitative data. I
would also like to thank Dr. Prashanth NS (IPH) and Dr. Upendra Bhojani (IPH) for their thought-provoking
comments that helped me better understand the present study in a larger context. I would like to
acknowledge the entire IPH team for welcoming me and fostering a supportive and friendly work
environment.
I am thankful to my supervisor at SOCHARA, Mr. Sabu KU, who helped me with the data analysis and Mr.
Chander SJ who introduced me to IPH. I would like to specially thank, Dr. Rahul ASGR, who helped me at
various stages of the research study, including meticulously reviewing the research topic guide, consent
forms and the final research report. I am grateful to the entire SOCHARA family, including Dr. Adithya
Pradyumna and Mr. Prasanna Saligram, for their valuable inputs that helped steer me in the right
direction.
Lastly, I would like to express my deep gratitude to Dr. Thelma Narayan (SOCHARA) for not only giving me
an opportunity to be part of the Community Health Learning Program (CHLP) but also encouraging me to
challenge myself and explore new perspectives to better understand complex scientific/social problems.
35
References
1. WHO. Global status report on noncommunicable diseases 2010 [Internet]. Description of
the Global Burden of NCDs Their Risk Factors and Determinants Geneva World Health
Organization. 2011 p. 176. Available from:
http://www.who.int/nmh/publications/ncd_report2010/en/
2. International Diabetes Foundation (IDF). IDF Diabetes Atlas, 6th Edition.
http://www.idf.org/diabetesatlas/download-book (accessed 8 August 2014).
3. World Heart Foundation. Cardiovascular disease risk factors: Hypertension.
http://www.world-heart-federation.org/cardiovascular-health/cardiovascular-disease-riskfactors/hypertension/ (accessed 8 August 2014).
4. Anand MP. Epidemiology of Hypertension. In: Anand MP and Billimoria AR eds.
Hypertension an international monograph 2001. New Delhi. IJCP 2001;10-25.
5. Ramachandran A: A breeding ground for diabetes. Diabetes Voice 2002, 47(1):18-20.
6. National Building Organisation: Report of the committee on slum statistics/census. New
Delhi: Ministry of Housing and Urban Poverty, Government of India; 2010
[http://www.mhupa.gov.in/W_new/Slum_Report_NBO.pdf], (accessed 8 August 2014).
7. Agarwal S: The state of urban health in India: comparing the poorest quartile to the rest of
the urban population in selected states and cities. Environment & Urbanization 2011,
23(1):13-28.
8. Bhojani U, Mishra A, Amruthavalli S, Devadasan N, Kolsteren P, De Henauw S, et al.
Constraints faced by urban poor in managing diabetes care: patients’ perspectives from
South India. Glob Health Action [Internet]. 2013 Jan;6(6):22258. Available from:
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3790910&tool=pmcentrez&ren
dertype=abstract
9. Selvaraj S, Karan AK. Deepening Health Insecurity in India: Evidence from National Sample
Surveys since 1980s. Econ Polit Wkly. 2009;44:55–60.
10. Balarajan Y, Selvaraj S, Subramanian S. Health care and equity in India. Lancet.
2011;377:505–15.
11. Banerjee A, Jadhav S, Khedkar D, Bhawalkar J, Rathod H. Access to health services among
slum dwellers in an industrial township and surrounding rural areas: A rapid epidemiological
assessment. Journal of Family Medicine and Primary Care. 2012. p. 20.
12. Bhojani U, Thriveni B, Devadasan R, Munegowda C, Devadasan N, Kolsteren P, et al. Out-ofpocket healthcare payments on chronic conditions impoverish urban poor in Bangalore,
India. BMC Public Health [Internet]. BMC Public Health; 2012 Jan [cited 2014 Jul
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20];12(1):990. Available from:
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3533578&tool=pmcentrez&ren
dertype=abstract
13. Institute of Public Health. Urban Health Project. http://www.iphindia.org/urban-healthproject/ (accessed 9 August 2014).
14. Ghosh S. Catastrophic Payments and Impoverishment due to Out-of-Pocket Health
Spending. Econ Polit Wkly. 2011;xlvi:63–70. hosh S.
15. Garg CC, Karan AK. Reducing out-of-pocket expenditures to reduce poverty: A
disaggregated analysis at rural-urban and state level in India. Health Policy Plan.
2009;24:116–28.
16. Bhojani U, Beerenhalli TS, Devadasan R, Munegowda CM, Devadasan N, Criel B, et al. No
longer diseases of the wealthy: prevalence and health-seeking for self-reported chronic
conditions among urban poor in South India. BMC Health Serv Res 2013; 13: 306.
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generic and branded medicines. International Journal of Pharmacy and Pharmaceutical
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Among Drug Retailers and Community Pharmacists. Indian J Pharm Sci. 2012;74(6): 571–
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Among Drug Retailers and Community Pharmacists. Indian J Pharm Sci. 2012;74(6): 571–
575.
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APPENDIX 1: Topic Guide for in-depth interviews
1. Self Introduction
Introduce myself and briefly explain the study. Inform them about their rights as
voluntary participants of the study and make sure they are comfortable to start the
interview.
2. Patient history of diabetes and hypertension
Question: I am aware that you have diabetes (and/or hypertension). Can you tell me more
about it?
Probes:
• For how long have you had the disease?
• What were your initial symptoms?
• Who diagnosed you and where?
• How many doctors did you go to before being diagnosed?
• Which clinic do you go to?
• Who is your doctor?
• Where do you get your blood sugar levels checked?
• How far is the clinic/diagnostic center from your house?
• Do you go to the same clinic/doctor/diagnostic center everytime?
• How often do you see the doctor?
o When was the last time you saw the doctor?
Do you go to the doctor for follow up as suggested by her or him?
• Are you currently taking any medicines?
o If not, what are the reasons?
o If yes, what are the medicines? If you have the necessary medicines with you
NOW, can you please show them to me?
• Do you take the medicines regularly?
o If not, what are the reasons?
• Where do you buy the medicines?
• How much do you spend on the medicines per week/per month?
• How do you manage to pay for these medicines? Where do you get this money?
• How much do you spend per month in total for your diabetes/hypertension care? This
includes consultation fees, lab tests, travel costs and other miscellaneous expenses.
• Have you been admitted to any hospital with diabetes or hypertension? If yes, please
provide the details.
• Does anyone in your family have the disease?
• How often do you eat in a day? (explore diet)
38
•
•
o At what times do you eat breakfast, lunch and dinner?
o Do you eat in-between?
o How often do you eat non-veg food/fried food/sweets?
o What do you usually eat and what do you avoid?
What do you do for exercise?
o How often do you exercise?
o For how long?
What do you do when you are stressed?
3. Awareness about the IPH clinic
Question: Have you heard of the IPH clinic? Can you tell me what you know about it?
Probes:
• Who told you about the clinic? Where did you find out about the clinic?
• Where is the clinic located?
• What are the timings?
• Who treats you there? (doctors, nurses etc)
o What do you know about the doctors at the clinic? (MBBS, Ayurvedetc)
• What are the services offered in the clinic?
o Do you know that you will be given a health card?
▪ If yes, what do you know about the benefits of the health card?
o Do you know that medicines are also dispensed?
▪ If yes, what do you know about the medicines that are dispensed?
(Branded, generic etc)
o Do you know if counseling is provided?
• Do you know that you are entitled to get all this for free?
4. Reasons for not utilizing the IPH clinic:
Question: It looks like you are not coming to the IPH clinic. Are there any reasons for not
utilizing the services?
Probes:
• How far is the IPH clinic from your house? (Explore physical barriers)
o (if they say distance is a problem) If the Community Health Workers (CHWs)
deliver the medicines every month to your house and you come to the clinic
ONLY once in 3 months, what do you think about it?
• What do you feel about the IPH clinic timings?(Explore physical barriers)
• What do you feel about the medicines that are dispensed in the IPH clinic?
39
•
•
•
•
o What is your opinion on low-cost medicines?
o What do you know about generic medicines?
o Have you used generic medicines before? If yes, what has been your
experience?
Do you know the building in which the IPH clinic is located? (If yes, ask the following)
o Do you know who is in charge of the building? (Explore political/cultural
barriers)
o Do you know that there is a dialysis center in the same building?
o What do you feel about having two centers – the IPH clinic and the dialysis
center in the same building?
(If patient is going to another clinic) What are the reasons that you go to ‘x’ clinic and
not go to the IPH clinic?
(If patient had been to IPH clinic before and is now going to another clinic) What made
you shift from the IPH clinic to your current clinic?
o What do you feel about the IPH clinic when compared to your current clinic?
o What do you like and dislike about your current clinic?
o What do you feel about the doctors in your clinic when compared to the IPH
clinic?
o What are the services in your current clinic that are not available in the IPH
clinic? What do you like about these services?
o What are the services in the IPH clinic that are not available in your current
clinic? What do you like about these services?
o How do you cope with the extra expenses of your current clinic when compared
to the IPH clinic?
What does your family feel about the IPH clinic? (Explore familial barriers)
o Does your husband/children/other family member approve of you going to the
IPH clinic?
5. Suggestions
•
Question: You mentioned certain positives and certain negatives about the IPH clinic
(Summarize them). Can you please tell us how we can improve the clinic?
Probes:
• What should we do in the community to increase awareness about the clinic?
• What other services would you like? (Ask for suggestion both inside and outside the
clinic)
• How can we help you in the long-term to manage your disease?
• Is there anything else we can do at the community level to help people with diabetes
and hypertension?
40
APPENDIX 2: Participation Information Sheet
Title: Understanding the barriers experienced by the people of an urban slum in
Bangalore to access primary diabetes and hypertension care in the Institute of Public
Health (IPH) Clinic
My name is AnushaPurushotham. I am a student of the Community Health Learning Programme in
an NGO called SOCHARA (Society for Community Health Awareness, Research and Action) in
Bangalore. As part of this programme, I am conducting a research study along withthe Institute of
Public Health (IPH) in your area to understand more about people living with diabetes (“sugar”) and
hypertension (“BP”). I would like to kindly request your permission to participate in this study.
This note provides an explanation of the nature of the research. This sheet may contain words that
you do not understand. If there is anything you need clarity on, please feel free to ask me. At the end
of this information sheet you will find my contact details.
Non-communicable diseases (NCDs) like diabetes (“sugar”) and hypertension (“BP”) have increased
over the past few years. People with these diseases face many problems in managing their care because
of several reasons. One such reason is the high-cost of treatment. I would like to understand why
people who are eligible for free services and medicines for diabetes and hypertension in the IPH clinic
are still not going to the clinic.
I would like to ask you a few questions about the history of your disease, your past and current
experiences in different clinics/hospitals and your opinions about the IPH clinic. Your answers will
be extremely important in helping us understand the reasons that prevent people from accessing health
care.
The questions can be very personal in nature and you can refuse to answer them if you do not feel
comfortable. Your participation in the study is voluntary and you can withdraw at any time during the
interview. You do not have to give any reasons for not answering questions or withdrawing from the
interview.
The interview will be approximately 15-20 minutes long. With your permission, I will record the
interview on a digital voice recorder. If you are not comfortable with this, please let me know and I
can record the interview in writing instead. Also, with your consent, your words will be reproduced
verbatim for the purposes for creating a report that may be published. I assure you that everything
you say will be confidential and your identity will be protected. All confidential data will be handled
only by me and the research team at the Institute of Public Health. All the information you provide
will be used only for present and future research purposes. If the information is published, any details
that identify you will not be made public. You have the right to view the information we collect from
you and also the right to deny usage of your details at any time.
41
There are minimal risks in participating in the study. Absolutely no physical risks are involved and the
interview will be conducted with utmost respect to your privacy.You will not receive any resource
benefits for participating in the study. However, the information you provide might help us offer
suggestions to improve the services in your area.
Your consent is required for your participation in the study. You can decide to participate or not. You
will be given a consent form to sign before the interview. Please let me know if you have any questions
or concerns. I will happy to answer them.
For further information or clarification, please contact us as follows –
AnushaPurushotham, Phone: +91- 9740396872
Dr.Mrunalini, Phone: +91-9611260563
Email: mail@iphindia.org
Postal address: 250, 2C Main Road, 2C Cross, Girinagar 1st phase, Bangalore - 560062
Thank you for your time. This sheet is for you to keep.
42
APPENDIX 3: Participant Consent Form
Title:Understanding the barriers experienced by the people of an urban slum in
Bangalore to access primary diabetes and hypertension care in the Institute of Public
Health (IPH) Clinic
I have read and understood the participation information sheet (or it has been read to me). I understand
that it involves me taking part in an interview. I have been explained the purpose and procedure of the
study. I have been informed that there will be no direct benefits for me. I understand that the information
I will provide is confidential and will not be disclosed to any other party or in any reports that could lead
to my identification. I also have been informed that the data from study can be used for preparing reports
and that reports will not contain my name or identification characteristics. I have been provided with the
name and contact details of the researcher whom I can contact. All my questions have been answered to
my satisfaction. I had enough time to decide whether I am going to participate or not. I know that I am
participating as a volunteer and I can step out of the program whenever I want and it is not necessary to
give an explanation. I know that research team will see my details. I give consent for my details to be used
for the research purposes mentioned in this form. All information regarding consent and purpose of the
study has been explained to me in the language I understand.
I provide consent to the following•
Participation in the in-depth interview:
Yes □
No □
•
Audio-recording of the in-depth interview:
Yes □
No □
•
Publishing of words/sentences spoken in interview verbatim:
Yes □
No □
………………………………………………
Name of Research Participant
………………………………………………
Name of Researcher
…………………………………………………
………………………………………………
Signature of Research Participant
Signature of Researcher
_____________________
Date
______________________
Date
43
If illiterate
I have witnessed the accurate reading of the consent form to the potential participant, and the individual
has had the opportunity to ask questions. I confirm that the individual has given consent freely.
Name of witness___________________________
Thumb print of participant
Signature of witness__________________________
Name of participant
___________________________
Date________________________
REVOCATION OF CONSENT
I hereby wish to WITHDRAW my consent to participate in the study described above and understand
that such withdrawal WILL NOTjeopardise my relationship with the Institute of Public Health.
Signature of participant
Name of Participant
______________________
_____________________
Date
______________
OR
Thumb print of participant
Name of Participant
Name of Witness
_____________________
__________________
Signature of Witness
Date
_____________________
________________
44
APPENDIX 4: Snapshots from the field
Snapshots of Slum A
45
Generic medicines stock in
the IPH Clinic
Dispensing generic
medicines in the IPH
clinic
A private School in KG Halli
46
Aerial view of a neighbourhood in KG
Halli
Street view of a neighbourhood in KG
Halli
Corporation quarters: A former slum
in KG Halli that was razed down and
replaced by building quarters
47
Position: 3923 (1 views)