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NCT02181881 Clinical Trial

DuoPACT Pilot Intervention

HIV/AIDS Clinical Trial

Official title:
Relationship Factors and HIV Treatment Adherence

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02181881
Other study ID # R01NR010187
Secondary ID R01NR010187
Status Completed
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date September 2014

Study information
Verified date February 2024
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators will pilot test the intervention by randomizing 30 couples to one of three conditions: 1) DuoPACT, the newly-developed couples intervention; 2) Life Steps, a standardized antiretroviral adherence intervention for HIV+ individuals; and 3) a treatment as usual (TAU) assessment-only control condition. After randomization, intervention sessions will be delivered weekly (6 DuoPACT sessions, or 3 Life Steps sessions). All couples will be assessed pre/post intervention to evaluate intervention acceptability and feasibility.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Gay male couple. 2. One or both partners must be HIV positive and on antiretroviral medications. Exclusion Criteria: Must be able to consent to and follow study protocol.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• DuoPACT
Intervention sessions are administered weekly by a counselor.
• Life Steps
Intervention sessions are administered weekly by a counselor.

Locations
Country Name City State
United States Center for AIDS Prevention Studies San Francisco California

Sponsors (2)
Lead Sponsor Collaborator
University of California, San Francisco National Institute of Nursing Research (NINR)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Satisfaction with the intervention All participants are assessed post intervention to evaluate intervention satisfaction and acceptability. 3 months
Secondary Feasibility All participants are assessed post intervention to evaluate the study's feasibility. 3 months
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