Improving HIV clinic environments to reduce stigma
Welcoming by Design Pilot: Reducing Structural Stigma by Changing Clinic Systems and Architectural Design to Make HIV Clinics More Friendly, Private, and Patient-Centric
This study is testing whether changing the look and feel of HIV clinics in Uganda can make patients feel more welcome and reduce stigma around HIV.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Minnesota Academic / other |
| Locations | 1 site (Minneapolis, Minnesota) |
| Trial ID | NCT05642676 on ClinicalTrials.gov |
What this trial studies
This study aims to assess the feasibility and acceptability of modifying clinic systems and architectural designs in Uganda to enhance the aesthetics, welcome, and privacy of HIV clinics. By implementing these changes, the study seeks to reduce stigma associated with HIV, improve patient retention in care, and enhance the overall patient experience. The evaluation will include surveys to determine if the modifications disrupt clinic operations or improve patient interactions. The pilot focuses on two specific HIV intervention clinics.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are enrolled in the participating HIV clinics.
Not a fit: Patients who are unable to provide consent or do not speak English or Luganda may not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly improve the experience of HIV patients, leading to better retention in care and reduced stigma.
How similar studies have performed: While this approach is innovative, similar studies focusing on reducing stigma through environmental changes have shown promise in other contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults 18 and older * Enrolled in the HIV clinics where we are working * Able to independently consent for interview, survey, or focus group. Exclusion Criteria: * Unable to provide consent * Does not speak English or Luganda (local language around Kampala and Entebbe)
Where this trial is running
Minneapolis, Minnesota
- University of Minnesota — Minneapolis, Minnesota, United States (Recruiting)
Study contacts
- Study coordinator: Sarah Lofgren, MD
- Email: lofg0020@umn.edu
- Phone: 6126244171
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.