Developing an HIV Disclosure Intervention for Men in Uganda

N/ANot Yet RecruitingNCT05771519

Brigham and Women's Hospital70 enrolled

Overview

The goal of this clinical trial is to test an HIV disclosure intervention that the investigators are developing focused on men living with HIV in Uganda. The main questions the investigators are trying to answer is whether the HIV disclosure intervention the investigators develop will help men who receive this intervention to disclose their HIV status to a greater extent than men who receive standard care. Participants assigned to the intervention group will likely participate in the following: * Sexual health education * Cognitive behavioral therapy strategies * Problem-solving skills building * Motivational interviewing * Developing a personalized HIV disclosure plan * Communication skills building * Role-playing disclosure strategies

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

HIV Infections Sexually Transmitted Infections (Not HIV or Hepatitis)

Interventions

Eligibility

Sex: MALEMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

For all 3 Aims, "index participants" inclusion criteria will include: * men living with HIV * with sexually transmitted infection symptoms (e.g., urethral discharge, genital lesions) * either not accessing antiretroviral therapy (per self-report109 and/or clinic documentation) or accessing antiretroviral therapy without HIV viral suppression * age ≥18 years, * with at least one sexual partner in the past three months Aims 2 and 3 have the additional inclusion criteria: * men living with HIV without HIV disclosure to at least one partner. In Aims 2 and 3, male participants will be encouraged to invite sexual partners for enrollment. These "partner participants" will have the following inclusion criteria: * age ≥18 years * partnered with an enrolled man who reports HIV disclosure or plans for HIV disclosure with study support * referred by the male participant. Exclusion Criteria: * an inability to speak the local language (Runyankole) or English * an inability to provide informed consent

Outcomes

Primary Outcomes

HIV disclosure intervention acceptability

Of 35 intervention participants, ≥70% (25 participants) rate all 4 items on the Acceptability of Intervention Measure (a 5-point Likert scales) as "agree" or higher. I will also assess intervention acceptability through qualitative interviews with participants and counselors.

Time frame: 6 months

HIV disclosure intervention feasibility

Feasibility is defined by the Feasibility of Intervention Measure, intervention fidelity, and session completion. A) Feasibility of Intervention Measure: Of 35 intervention participants, ≥70% (25 participants) rate all 4 items on the Feasibility of Intervention Measure (a 5-point Likert scale) as "agree" or higher, B) Fidelity: Assuming a five-session intervention with 25% English-transcribed (44/175 sessions), intervention fidelity is attained when ≥70% (31 sessions) achieve ≥90% fidelity to the protocol adherence checklist, C) Session completion: Of the 35 intervention participants, ≥70% attend ≥50% of sessions. I will also assess intervention acceptability through qualitative interviews with participants and counselors.

Time frame: 6 months

Secondary Outcomes

Index participant-reported disclosure

Index participant-reported disclosure (measured by an expanded disclosure measurement tool and a Center For AIDS Research-funded HIV Disclosure Processes Model Measurement Scale in development.

Time frame: 6 months

Partner participant HIV study site/clinic testing and counseling

The investigators will measure the percentage of partners that participants bring to clinic for HIV testing.

Time frame: 6 months

HIV viral suppression

Participant HIV viral suppression measured by nucleic acid amplification testing.

Time frame: 6 months

Developing an HIV Disclosure Intervention for Men in Uganda

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts