Actively Recruiting
Latinx Hazardous Drinkers With Clinical Anxiety: Effectiveness Trial of a Personalized Normative Feedback Intervention
Led by University of Houston · Updated on 2024-06-07
250
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Houston
Lead Sponsor
N
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying a brief, computer-based personalized feedback intervention designed specifically for Latinx adults who have hazardous drinking habits and clinical anxiety. The goal is to understand if this culturally adapted approach can improve knowledge about how anxiety and alcohol misuse relate, increase motivation to reduce drinking, and change attitudes toward using alcohol to manage anxiety. The study includes two phases: the first to refine the intervention with feedback, and the second to test its effectiveness through a randomized trial. In the second phase, participants are randomly assigned to receive either the culturally adapted Alcohol-Anxiety Personalized Feedback Intervention (AA-PFI 2.0) or a control intervention focusing on exercise and nutrition (C-PFI). Both interventions are brief, computer-delivered sessions lasting about 20 to 30 minutes. Initial screening is done by phone, while baseline and post-treatment assessments take place in person. Follow-up data is collected remotely at 1, 3, and 6 months after treatment. Participants will complete questionnaires and assessments measuring motivation to reduce drinking, attitudes toward alcohol use related to anxiety, and drinking motives, both before and after the intervention. Additional measures include anxiety severity and alcohol use disorder symptoms tracked up to six months later. The study monitors changes over time to evaluate the intervention's impact, and participation involves initial visits and several remote follow-ups over half a year.
CONDITIONS
Brief Title
Personalized Feedback Intervention for Latinx Drinkers With Anxiety
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be between 21 and 75 years old
- Self-identify as Latinx or Hispanic
- Be fluent in Spanish
- Meet criteria for current hazardous drinking
- Meet criteria for clinical anxiety
- Be able to provide written, informed consent
You will not qualify if you...
- Currently involved in an alcohol or other substance use program
- Currently pregnant
- Currently receiving psychotherapy for anxiety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 telephone screening visit
Duration - 1 day
Participants complete a brief, culturally adapted, computer-delivered personalized feedback intervention targeting alcohol misuse and anxiety, or a control intervention on exercise and nutrition.
1 baseline visit (in-person) to complete the intervention and baseline assessments
Duration - 6 months
Participants complete follow-up assessments remotely to monitor changes in alcohol use and anxiety over time.
3 remote follow-up assessments at 1, 3, and 6 months post-intervention
Trial Site Locations
Total: 1 location
1
RESTORE Laboratory: Research on Emotion, Substance Treatment Outcomes, and Racial Equity
Houston, Texas, United States, 77204
Actively Recruiting
Research Team
B
Brooke Y Kauffman, Ph.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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