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N/A N=151 Other

Addressing Drug Use Stigma in Human Immunodeficiency Virus (HIV) Care and Treatment Clinics in Tanzania

Drug Use Stigma in HIV Treatment Clinics

Enrolled (actual)
151
Serious AEs
Results posted
Feb 2024
Primary outcome: Primary: Modified Opening Minds Scale for Health Providers (OMS-HC) — 22.92; 16.82 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Drug-use stigma reduction intervention for HIV care and treatment clinic staff (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
RTI International
Primary completion
Jul 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Modified Opening Minds Scale for Health Providers (OMS-HC)
22.92; 16.82
PRIMARY
Feasibility of Intervention Measure
4.7
PRIMARY
Acceptability of Intervention Measure
4.72
PRIMARY
Appropriateness of Intervention Measure
4.82
SECONDARY
Knowledge About Drug Use and How to Provide HIV Services to People Who Use Drugs
3.4; 4.37
SECONDARY
Modified Bogardus Social Distance Scale
12.6; 8.34

Summary

The goal of this study is to adapt and pilot an effective health facility HIV stigma-reduction intervention to address drug use stigma in human immunodeficiency Virus (HIV) Care and Treatment clinics (CTCs) in Tanzania, a barrier to HIV care for People Living with HIV (PLWH) who use drugs. In Tanzania, there are an estimated 300,000 People Who use Drugs (PWUD), primarily heroin. HIV prevalence among PWUD who do not inject (18-25%) and those who do inject (35%) is 4-7 times higher than in the general population (5%). PWUD face high levels of stigma, including when they try to seek HIV treatment at HIV CTCs, presenting a barrier to linkage and retention in HIV treatment for this highly HIV vulnerable group. Reducing drug use stigma in HIV CTCs is critical to improving access to and retention in HIV treatment services for PWUD. In response to this need, the investigators will: 1) Adapt a health facility HIV stigma-reduction participatory training intervention to address drug use stigma in HIV CTCs (Aim 1). 2) Pilot test the adapted drug use stigma-reduction intervention for acceptability, appropriateness, and feasibility (Aim 2). The investigators will achieve Aim 1 through a systematic, multi-stage adaptation process that will include a formative phase of in-depth interviews with PLWH who use drugs and CTC staff to inform initial adaptation of the Health Policy Plus (HP+) intervention. Stakeholders, including PLWH who use drugs and CTC staff, will provide feedback on the initial materials through a participatory workshop, leading to a training manual that will be reviewed by topic experts and then finalized. Experienced Tanzanian HIV stigma-reduction trainers will deliver the intervention to CTC staff. The pilot test will include 150 staff (the study participants) based in seven CTCs in Dar-es-Salaam. A mixed methods evaluation will comprise pre-post surveys, observation of trainings, and post-training focus group discussions with staff (study participants) who complete the intervention and trainers. Changes in CTC staff (study participants) mean scores on stigma scales from pre- to post-intervention will be assessed, along with measures of intervention acceptability, appropriateness, and feasibility (measured at end line only). Post-intervention focus group discussions will explore themes around the experience of participating in the drug use stigma-reduction training.

Eligibility Criteria

Inclusion Criteria

Intervention pilot testing phase:

-This will include CTC staff and other staff within the medical facility where the CTC is physically housed who come into direct contact with clients attending the CTC (guards, receptionists, lab and pharmacy staff), who work in one of the seven clinics selected for this study.

Exclusion Criteria

  • Under the age of 18.
  • Refusal to Consent.
  • PLWH participants who appear to be too impaired to provide informed consent or answer questions accurately will be ineligible.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04863898). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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