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Behavioral Intervention
Cognitive Behavioral Therapy for Alcohol Use Disorder in HIV (TALC Trial)
N/A
Recruiting
Led By Karen Cropsey, Psy.D.
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
18 years of age or older
Be older than 18 years old
Must not have
Active suicidality or psychosis
Inability to use a mobile phone due to cognitive or physical impairments
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial will test if a cognitive-behavioral intervention can help people with HIV who struggle with unhealthy alcohol use and comorbid mental health symptoms.
Who is the study for?
This trial is for adults over 18 living with HIV in Alabama who drink alcohol at levels considered unhealthy. They must be getting care at certain clinics and able to use a mobile phone. People with active suicidal thoughts, psychosis, risk of severe alcohol withdrawal, or those who can't speak English well enough for therapy are not eligible.
What is being tested?
The study tests if adding cognitive-behavioral therapy (CETA) via telemedicine to a brief intervention helps reduce unhealthy alcohol use and improve mental health and HIV outcomes better than the brief intervention alone.
What are the potential side effects?
Since this trial involves behavioral interventions rather than medications, typical drug side effects are not expected. However, participants may experience discomfort discussing personal issues during therapy sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am not currently experiencing thoughts of suicide or psychosis.
Select...
I cannot use a mobile phone because of cognitive or physical issues.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change from Baseline Alcohol Use at 6 months
Secondary study objectives
Change from Baseline Anxiety at 12 months
Change from Baseline Anxiety at 6 months
Change from Baseline Depression at 12 months
+7 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Common Elements Treatment Approach (CETA) via TelemedicineExperimental Treatment2 Interventions
Participants will be provided with 6 to 12 weekly CETA sessions via telephone.
Group II: Alcohol Brief Intervention (BI)Active Control1 Intervention
At the time of trial enrollment, participants will receive a session of alcohol brief intervention (BI) via telephone.
Find a Location
Who is running the clinical trial?
National Institute on Alcohol Abuse and Alcoholism (NIAAA)NIH
835 Previous Clinical Trials
1,082,566 Total Patients Enrolled
457 Trials studying Alcoholism
823,786 Patients Enrolled for Alcoholism
University of Alabama at BirminghamLead Sponsor
1,645 Previous Clinical Trials
2,342,544 Total Patients Enrolled
4 Trials studying Alcoholism
1,854 Patients Enrolled for Alcoholism
Karen Cropsey, Psy.D.Principal InvestigatorUniversity of Alabama at Birmingham
1 Previous Clinical Trials
4 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 years old or older.I am not currently experiencing thoughts of suicide or psychosis.I cannot use a mobile phone because of cognitive or physical issues.
Research Study Groups:
This trial has the following groups:- Group 1: Alcohol Brief Intervention (BI)
- Group 2: Common Elements Treatment Approach (CETA) via Telemedicine
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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