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Welcoming by Design Pilot: Reducing Structural Stigma by Changing Clinic Systems and Architectural Design

Not Applicable
Not yet recruiting
Conditions
Hiv
Interventions
Other: Clinics remodeling
Registration Number
NCT05642676
Lead Sponsor
University of Minnesota
Brief Summary

The purpose of this study is to test the feasibility and acceptability of implementing clinic system changes and physical structures in Uganda to improve aesthetics, welcome, and privacy to reduce HIV stigma, improve retention-in-care, and improve the patient experience.

To evaluate pilot/implementation outcomes, the outcomes of fidelity, feasibility, and acceptability will be assessed prior to intervention. After the changes are done to two HIV interventions clinics, the outcome surveys will assess if the changes were disruptive or impeded the workings of the clinics.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
100
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)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Interventions clinics to be remodeledClinics remodeling-
Primary Outcome Measures
NameTimeMethod
Feasibilitybaseline

An assessment of the practicality of a proposed idea or project, by assessing recruitment capacity, and ability to complete proposed modifications in clinics. The intervention will be judged feasible if enrollment and metrics can be completed.

Acceptability surveyBaseline

How well an intervention will be received by the target population and the extent to which the intervention meets the needs of the target population and organizational setting. This will be assessed through qualitative evaluation and a quantitative survey from patients and staff.

Fidelity to the Intervention6-months post intervention

Assesses whether the intervention was delivered as intended, using the intervention plan/checklist

Outcomes survey6-months post intervention

assesses if the changes were disruptive or impeded the workings of the clinics.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

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