| Literature DB >> 33353996 |
Anand Krishnan1, Rajesh Tandon2, Baridalyne Nongkynrih1.
Abstract
Community-based participatory research (CBPR) is an approach in which researchers undertake research in partnership with those affected by the issue being studied, for the purpose of taking action or effecting social change. It can also incorporate those who will use the results to change practice and inform policy. The practice of CBPR is primarily focused on "Knowledge for Change." Most research projects in such CBPR partnerships are funded through the academic partners. In many situations, academic and professional researcher institutions and researchers find it difficult to share the information and resources or to directly engage with local community and other local stakeholders. In practice, finding an intermediary partner who has good rapport with local community and local government can be very effective. While there are good initiatives in selected medical colleges for community orientation of medical undergraduates and postgraduates in community medicine, these are not immersive enough to cause an attitudinal change. It is time that we exposed our graduates and postgraduates to CBPR concepts and practice. Copyright:Entities:
Keywords: Community medicine; community-based participatory research; teaching
Year: 2020 PMID: 33353996 PMCID: PMC7745794 DOI: 10.4103/ijcm.IJCM_343_19
Source DB: PubMed Journal: Indian J Community Med ISSN: 0970-0218
Some examples of health-related participatory research methods in India and other developing countries
| Topic addressed | Participants | Study design | Areas of community involvement | Results |
|---|---|---|---|---|
| Menstrual hygiene[ | Female adolescents and young adults; Wardha district, Maharashtra, India | Quantitative and qualitative: Data collected through surveys and focus groups | Participated in needs assessmentReviewed health education materialsDelivered educational programParticipated in evaluation | Increased participation in community-based organizations and village-based health programs. Increased awareness of menstruation, use of readymade pads; increase in health-seeking behavior following symptoms of an STI or reproductive infection |
| Infant health[ | Women, female adolescents, other members of community; Maharashtra, India | Quantitative and qualitative: Data collected through surveys and focus groups | Participated in formative surveys and focus groups; review of health education materials; selection and supervision of CHWs; health education sessions; evaluation of the health education program | Women’s participation strengthened their social and health insurance status. Women had more knowledge regarding newborn danger signs. There was an increase in seeking healthcare for a sick newborn |
| HIV/AIDS[14] | Adult women (age 18 or greater) taking antiretroviral therapy; rural areas near Chennai, India | Qualitative: focus groups with women living with HIV/AIDS; healthcare providers, and ASHAs | Participated in Community Advisory Board; assisted in identifying women living with AIDS; participated in focus groups. Refined interview guide; helped shape the intervention program being designed. | Revealed several barriers to ART adherence including illness, financial, traveling long distances, lack of child care, stigma, psychological problems. Found that social support would be beneficial. Women would like to receive care at the primary health centers closer to their homes. |
| ORS use in Nicaragua[ | Mothers of children with diarrhea | Qualitative | A study in Nicaragua on people’s concept of diarrhea and dehydration in children | Mothers were reluctant to use ORS because they were disappointed that its usage did not lead to expected results of stopping diarrhea. The information that was given to the caretakers or mothers placed emphasis on how to use ORS and not on how it works and on its effects |
| Hypertension awareness, prevention, and treatment in Zimbabwe[ | The CIG included hypertensive patients, VHWs and community leaders | Community hypertension care was established through competence training of VHWs. The CIG members were involved in designing intended themes for outcomes and possible strategies to achieve the outcomes | A “CIG hypertension club” comprising all CIG members was designed to encourage all members to get their blood pressure recorded and publicly share their recordings. Group interpretation of readings would be done, and quantitative output variables such as pill pickup rate, attendance to reviews, compliance to treatment (pill counts), and blood pressure control were measured for PLWHT in the “club.” The “clubs” were decentralized to the community revolving around the VHWs to enable community screening, peer support, and health education | This project empowered the community and VHW was established as a key link between the community and the formal health delivery. This was a sustainable form of improving community hypertension health outcomes by positively influencing beliefs and behaviors. It was seen that there was an improvement in knowledge about awareness and primary prevention of hypertension. Pill pickup rate and treatment compliance improved and the community’s confidence in VHWs was restored |
PLWHT: Persons living with hypertension, VHWs: Village health workers, CIG: Cooperative inquiry group, ORS: Oral rehydration solution, ASHAs: Accredited social health activist, STI=Sexually transmitted infections, HW=Community health workers
Comparison between traditional and community-based research
| Traditional research | Community-based participatory research | |
|---|---|---|
| Research objective | Issues identified based on epidemiologic data and funding opportunities | Identifying issues of greatest importance to the community with their full participation |
| Study design | Design based entirely on scientific rigor and feasibility | Community representative involved with study design |
| Recruitment | Approaches based on scientific issues of random sampling and maintaining high response rate | Community representatives provide guidance on recruitment and retention strategies and aid in recruitment efforts |
| Instrument design | Instruments adopted/adapted from other studies; tested chiefly with psychometric analysis method | Instruments developed with community input and tested in similar populations |
| Needs assessment data collection | Academic institution’s responsibility | Academic institution and community’s responsibility |
| Intervention design | Researchers design interventions based on literature and theory | Community members help guide intervention development |
| Analysis and interpretation | Researchers own the data, conduct analysis, and interpret the findings | Data are shared; community members and researchers work together to interpret results |
| Sustainability | Usually sustainability plan is not included | Sustainability is a priority the begins at a program’s inception |
| Dissemination | Results disseminated in scientific forum, published in peer-reviewed academic journals | Community assists researchers to identify appropriate venues to disseminate results; community members involved in dissemination; results are also published in peer-reviewed journals |