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COMPLETED
NCT05829759
NA

Telehealth Delivery (Tele-B6)

Sponsor: Emory University

View on ClinicalTrials.gov

Summary

The research team has developed an interventional group program for young men living with HIV and will be adapting it for telehealth delivery. The purpose of the study is to determine whether or not this program can help improve social connections and the health of young men in online delivery and evaluate its potential for implementation in a community setting. The study has three phases: (1) engaging a community advisory board to create and adapt the intervention for online delivery, (2) a randomized clinical trial of the online intervention, and (3) evaluation of the program for community implementation with our partner organization. Participants in the second phase of the study will meet with a study team member to discuss the research process and provide informed consent. The community organization employees will provide consent online prior to completion of a survey and indicate whether they consent to be contacted further for in-depth interviews.

Official title: Brothers Building Brothers by Breaking Barriers for Telehealth Delivery (Tele-B6)

Key Details

Gender

MALE

Age Range

18 Years - 29 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2023-04-18

Completion Date

2024-11-05

Last Updated

2026-04-20

Healthy Volunteers

No

Interventions

BEHAVIORAL

Tele-B6

Participants will be part of the Tele-B6 intervention that includes five group sessions delivered over the course of five weeks. Survey assessments for the intervention group (first phase) will be conducted at enrollment (baseline), 2 months (immediate post-intervention survey), 4 months (interim-survey, post-intervention), and 6 months (endline).

BEHAVIORAL

Delayed intervention (waitlist control)

Wait-list control participants will be assigned to initiate the full intervention at month 2 after their enrollment (i.e., after they and their corresponding intervention group have completed their intervention and one follow-up survey). Wait-list control participants will complete surveys at enrollment (baseline), 2 months (pre-intervention), 4 months (immediate post-intervention), and 6 months (endline).

Locations (1)

Grady Infectious Diseases Program Clinic

Atlanta, Georgia, United States