Evelyne Kestelyn
Biographic Data
| ID | 7033933 |
|---|---|
| NAME | Evelyne Kestelyn |
| GIVEN NAMES | Evelyne |
| FAMILY NAME | Kestelyn |
| SIGNATURE | KESTELYN E |
| AFFILIATIONS | Project Ubuzima |
| ORCID | 0000-0002-5728-0918 |
| VERIFIED | Yes |
| TOTAL WORKS | 5 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 5 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2012 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Data reuse in global health: Perspectives from actors in policy, funding and research
BACKGROUND: Data-sharing mandates from funders and journals have increased in recent years, but little is known about how shared data are used. Existing research has focused on access frameworks, with less attention to conditions that enable or hinder subsequent analyses and their impact on science and policy. METHODS: We conducted semi-structured interviews with 22 key informants with experience using clinical research data. Participants include…
Data sharing and reuse in clinical research: Are we there yet? A cross-sectional study on progress, challenges and opportunities in LMICs
Data sharing holds promise to accelerate innovative discoveries through artificial intelligence (AI) and traditional analytics. However, it remains unclear whether these prospects translate into tangible benefits in improving health care and scientific progress. In this cross-sectional study, we investigate current data reuse practices and explore ways to enhance the use of existing data in clinical research, focusing on low- and middle-income co…
Informed consent, community engagement, and study participation at a research site in Kigali, Rwanda
People enroll in medical research for many reasons ranging from decisions regarding their own or family members' health situation to broader considerations including access to health and financial resources. In socially vulnerable communities the choice to participate is often based on a risk‐benefit assessment that goes beyond the medical aspects of the research, and considers the benefits received. In this qualitative study, we examined the mot…
The ring plus project: Safety and acceptability of vaginal rings that protect women from unintended pregnancy
Clinicaltrials.gov NCT01796613 . Registered 14 February 2013
Joining and leaving sex work: Experiences of women in Kigali, Rwanda
Although sex work can bring significant economic benefit there are serious downsides, not least vulnerability to adverse sexual health outcomes. Focus-groups discussions and in-depth interviews were conducted with 70 female sex workers to explore the context in which they started sex work, their motivations to leave, and their experiences of trying to leave. The pathway to becoming a sex worker was underscored by poverty, with disruptive events l…
No prominent works on this page.
Joining and leaving sex work: Experiences of women in Kigali, Rwanda
Although sex work can bring significant economic benefit there are serious downsides, not least vulnerability to adverse sexual health outcomes. Focus-groups discussions and in-depth interviews were conducted with 70 female sex workers to explore the context in which they started sex work, their motivations to leave, and their experiences of trying to leave. The pathway to becoming a sex worker was underscored by poverty, with disruptive events l…
The ring plus project: Safety and acceptability of vaginal rings that protect women from unintended pregnancy
Clinicaltrials.gov NCT01796613 . Registered 14 February 2013
Informed consent, community engagement, and study participation at a research site in Kigali, Rwanda
People enroll in medical research for many reasons ranging from decisions regarding their own or family members' health situation to broader considerations including access to health and financial resources. In socially vulnerable communities the choice to participate is often based on a risk‐benefit assessment that goes beyond the medical aspects of the research, and considers the benefits received. In this qualitative study, we examined the mot…
Data sharing and reuse in clinical research: Are we there yet? A cross-sectional study on progress, challenges and opportunities in LMICs
Data sharing holds promise to accelerate innovative discoveries through artificial intelligence (AI) and traditional analytics. However, it remains unclear whether these prospects translate into tangible benefits in improving health care and scientific progress. In this cross-sectional study, we investigate current data reuse practices and explore ways to enhance the use of existing data in clinical research, focusing on low- and middle-income co…
Data reuse in global health: Perspectives from actors in policy, funding and research
BACKGROUND: Data-sharing mandates from funders and journals have increased in recent years, but little is known about how shared data are used. Existing research has focused on access frameworks, with less attention to conditions that enable or hinder subsequent analyses and their impact on science and policy. METHODS: We conducted semi-structured interviews with 22 key informants with experience using clinical research data. Participants include…
Medicine (4 works) · Family medicine (3 works) · Psychology (3 works) · Alternative medicine (2 works) · Data collection (2 works) · Data sharing (2 works) · Ethics in Clinical Research (2 works) · Focus group (2 works) · Qualitative research (2 works) · Research ethics (2 works)