MedTrace Logo

Mopati: A Pilot Hiv Treatment Partner Intervention In Botswana

NCT04796610 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2023-11-01

Study results available
· View outcomes & findings →

Summary

This study is a pilot test of the Mopati program ("partner" in Setswana), which is a multi-level intervention that guides healthcare providers and patients about treatment partner selection, and trains treatment partners on provision of effective support. The Specific Aims are: (1) To develop a multi-level treatment partner intervention with input from community and healthcare provider stakeholders in Botswana; and (2) To conduct a pilot test of the feasibility, acceptability, and preliminary effects on viral suppression.

Conditions

Interventions

BEHAVIORAL

Mopati

The intervention will provide training to health care providers on how to guide unsuppressed HIV patients in the selection of treatment partners. The Mopati program will provide education to patients and their treatment partners about HIV treatment and how treatment partners can support patients in treatment adherence.

Sponsors & Collaborators

  • Botswana Harvard AIDS Institute Partnership

    collaborator OTHER

  • Children's Mercy Hospital Kansas City

    collaborator OTHER

  • University of Botswana

    collaborator OTHER

  • RAND

    lead OTHER

Principal Investigators

  • Laura Bogart, PhD · RAND

  • Mosepele Mosepele, MD, MPH · University of Botswana & Botswana Harvard AIDS Institute Partnership

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-17
Primary Completion
2022-08-31
Completion
2022-08-31

Countries

  • Botswana

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04796610 on ClinicalTrials.gov