Skip to main content
Clinical Trials/NCT03238586
NCT03238586CompletedNot Applicable

HIV/AIDS & Alcohol-Related Outcomes: Translational Evidence-Based Interventions

Louisiana State University Health Sciences Center in New Orleans1 site in 1 country232 target enrollmentStarted: November 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
232
Locations
1
Primary Endpoint
Viral load

Study Overview

Brief Summary

A clinical study for patients with HIV that investigates the best way to reduce HIV transmission risk, and to improve the overall health of people living with HIV/AIDS. Participants will complete four assessments over the course of one year and will be randomly assigned to a five-week treatment program.

Detailed Description

The main purpose of this research study is to investigate the best way to reduce HIV transmission risk and to improve the overall health of people living with HIV/AIDS. This study tests an intervention program that aims to improve knowledge, motivation, and skills. The intervention program is designed to motivate participants to take their medications routinely, improve the quality of life for those living with HIV, and decrease risky behaviors that may lead to HIV transmission.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •HIV positive
  • •Recent alcohol use

Exclusion Criteria

  • Not provided

Arms & Interventions

Standard of Care

No Intervention

Five-week standard of care program.

WELL Program

Experimental

Five-week treatment program that aims to improve knowledge, motivation, and skills. It is designed to motivate participants to take their medications routinely, improve the quality of life for those living with HIV, and decrease risky behaviors that may lead to HIV transmission.

Intervention: WELL Program (Behavioral)

Outcomes

Primary Outcomes

Viral load

Time Frame: Change from baseline at 3 months, 6 months and 1 year

The primary outcome measure will be disease progression or more specifically, the proportion of patients achieving viral suppression.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Patricia Molina

Richard Ashman, PhD Professor and Head Department of Physiology; Director Alcohol and Drug Abuse Center of Excellence

Louisiana State University Health Sciences Center in New Orleans

Study Sites (1)

Loading locations...

Similar Trials