- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04491539
Adapting the Finding Respect and Ending Stigma Around HIV (FRESH) Intervention for the Dominican Republic
May 1, 2025 updated by: Henna Budhwani, Florida State University
This research has the potential to make important contributions toward HIV and intersectional stigma reduction across the Spanish-speaking Caribbean.
It will do so by adapting and testing a patient-provider, clinic-based intersectional stigma-reduction intervention -- Finding Respect and Ending Stigma around HIV (FRESH) -- for the Dominican Republic.
Preliminary results from this R21 study (e.g.
workshop satisfaction, stigma outcomes, HIV continuum of care outcomes, etc.) will inform the development of an investigator-initiated R01 proposal to conduct a full scale randomized controlled trial of the adapted FRESH intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The proposed study addresses the high level of stigma against people living with HIV (PLWH), particularly gender and sexual minorities, that is embedded in the Dominican Republic's HIV treatment system through the adaptation and testing of a patient-provider intervention -- Finding Respect and Ending Stigma around HIV (FRESH).
The Dominican Republic is a high priority setting with an increasing need for HIV stigma reduction studies.
The Caribbean holds the second highest regional burden of HIV in the world, yet receives insufficient HIV-related stigma research funding.
The Dominican Republic is 1 of 5 countries that accounts for over 95% of all Caribbean HIV infections; it also has a significant concentrated HIV epidemic, a deeply conservative society in which PLWH are stigmatized, and an exceptionally low national viral load suppression rate.
To accomplish this pilot study, three Specific Aims are proposed.
Aim 1 is to explore sources, characteristics, and consequences of HIV-related and intersectional stigmas experienced in healthcare settings to inform the adaptation of FRESH.
To accomplish Aim 1, we will conduct qualitative in-depth interviews with healthcare workers who provide HIV care, focus groups with MSM, and in-depth interviews with trans- women.
Aim 2 is to adapt FRESH to address stigmas experienced these individuals in the Dominican Republic.
We will apply the Aim 1 findings using the ADAPT-ITT framework to systematically adapt FRESH, an intervention that has been employed to reduce stigma in healthcare settings in Africa and the United States.
Through an iterative process, each revision of FRESH will be shared with both PLWH and healthcare workers to solicit and incorporate their feedback about each version of the adapted intervention.
Aim 3 will pilot-test the adapted intervention to obtain estimates of its ability to reduce stigmatizing attitudes and behaviors from HWs and experiences of stigma reported by sexual and gender minorities (SGM) and non-SGM clients living with HIV (primary); while exploring if FRESH has the potential to influence clinic-level outcomes.
By adapting and testing the FRESH intervention for the Spanish-speaking Caribbean, FRESH could become a validated, multi-region HIV and intersectional stigma reduction intervention designed specifically for healthcare settings in high-stigma, culturally conservative, resource-constrained communities; such a scientific development would be a significant contribution to HIV stigma reduction efforts in the Caribbean and globally.
Study Type
Interventional
Enrollment (Actual)
36
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Florida
-
Tallahassee, Florida, United States, 32306
- Florida State University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria for health worker participants:
- Minimally 18 years and 0 months of age
- Works at one of the three study sites
- Interacts with people living with HIV
- Spanish speaking
- Can read Spanish text
- Able and willing to provide informed consent
Inclusion Criteria for people living with HIV participants:
- Minimally 16 years and 0 months of age
- Is HIV-positive
- Spanish speaking
- Receives treatment at one of the three study sites
- Identifies as an SGM
- Able and willing to provide informed consent
Exclusion Criteria:
• Does not meet inclusion criteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Healthcare Workers or Providers
Healthcare Workers or Providers receiving the FRESH intervention.
Arm to test the intervention's effect on this specific population.
|
The Finding Respect and Ending Stigma around HIV (FRESH) intervention is theoretically informed by Social Cognitive Theory (SCT) and Interpersonal Contact theory (ICT) and was specifically designed for delivery in high-stigma settings, such as Dominican Republic.
FRESH was originally developed in Africa to address HIV-related stigma, and later was adapted to address intersectional stigmas experienced by sexual and gender minorities (SGM) living with HIV in the United States Deep South.
To our knowledge, FRESH will be the first intervention to address intersectional stigmas experienced by men who have sex with men, transgender women, and people living with HIV in clinical settings in the Spanish-speaking Caribbean.
|
|
Experimental: Clients
People with HIV Clients receiving the FRESH intervention.
Arm to test the intervention's effect on this specific population.
|
The Finding Respect and Ending Stigma around HIV (FRESH) intervention is theoretically informed by Social Cognitive Theory (SCT) and Interpersonal Contact theory (ICT) and was specifically designed for delivery in high-stigma settings, such as Dominican Republic.
FRESH was originally developed in Africa to address HIV-related stigma, and later was adapted to address intersectional stigmas experienced by sexual and gender minorities (SGM) living with HIV in the United States Deep South.
To our knowledge, FRESH will be the first intervention to address intersectional stigmas experienced by men who have sex with men, transgender women, and people living with HIV in clinical settings in the Spanish-speaking Caribbean.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HIV-related Stigma
Time Frame: Year 2
|
For providers, the results are reported for the Opinions about People with HIV sub-scale from the HIV-related stigma among health facility staff scale, 6 questions.
Response options are Strongly Agree, Agree, Disagree, and Strongly Disagree.
This scale does not include reverse coding.
Higher scores indicate higher levels of stigma.
The score can range from 5 (min) to 20 (max).
For clients, the results are reported for the Experiencing HIV-related Stigma in Healthcare Settings scale, 5 questions.
Response options are Never, Rarely, Sometimes, Usually, and Always.
This scale does not include reverse coding.
Higher scores indicate higher levels of stigma.
The score can range from 0 (min) to 20 (max).
|
Year 2
|
|
HIV Knowledge Index
Time Frame: Year 2
|
Results are reported for the HIV Knowledge Index from providers only.
This is not a validated scale but was being tested in the context of this study.
It included 13 homegrown questions.
Range was 0 (min) to 13 (max), with higher scores indicating greater knowledge.
|
Year 2
|
|
Empathy and Avoidance in Treating Patients Living With HIV/AIDS
Time Frame: Year 2
|
For providers, the results are reported for empathy and avoidance in treating patients living with HIV/AIDS, 11 questions.
Response options are Strongly Agree, Agree, Neutral, Disagree, and Strongly Disagree.
This scale includes reverse coding.
Higher scores indicate higher levels of stigma.
The score can range from 11 (min) to 55 (max).
|
Year 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Multiple Discrimination Scale - Orientation
Time Frame: Year 2
|
For clients, the results are reported for experiences of discrimination related to sexual orientation, 10 questions.
Response options are Yes and No. Higher scores indicate higher levels of stigma.
The score can range from 0 (min) to 10 (max).
|
Year 2
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 28, 2020
Primary Completion (Actual)
June 30, 2023
Study Completion (Actual)
June 30, 2023
Study Registration Dates
First Submitted
July 24, 2020
First Submitted That Met QC Criteria
July 28, 2020
First Posted (Actual)
July 29, 2020
Study Record Updates
Last Update Posted (Actual)
May 16, 2025
Last Update Submitted That Met QC Criteria
May 1, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 526497
- 5R21TW011761-02 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
All data gathered during the proposed study will be available to all participating investigators and institutions.
This includes the University of Alabama at Birmingham (UAB), Universidad Iberoamericana (UNIBE), and the Caribbean Vulnerable Communities Coalition (CVC).
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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