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NCT03238586 Clinical Trial

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

HIV/AIDS Clinical Trial

— WELL  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03238586
Other study ID # WELL
Secondary ID 1U01AA021995-01
Status Completed
Phase N/A
First received
Last updated
Start date November 2012
Est. completion date August 2019

Study information
Verified date February 2020
Source Louisiana State University Health Sciences Center in New Orleans
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 232
Est. completion date August 2019
Est. primary completion date July 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- HIV positive

- Recent alcohol use

Exclusion Criteria:

-

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• WELL Program

Locations
Country Name City State
United States University Medical Center New Orleans Infectious Disease Services New Orleans Louisiana

Sponsors (2)
Lead Sponsor Collaborator
Louisiana State University Health Sciences Center in New Orleans National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Viral load The primary outcome measure will be disease progression or more specifically, the proportion of patients achieving viral suppression. Change from baseline at 3 months, 6 months and 1 year
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