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Personalized Feedback Intervention for Anxiety and Hazardous Drinking
N/A
Recruiting
Led By Michael J Zvolensky, Ph.D.
Research Sponsored by University of Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Being between the age of 21 to 75 years of age
Being between the age of 21 to 75 years of age
Must not have
Current engagement in psychotherapy for anxiety
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline pre pfi completion to 6-months post pfi completion
Awards & highlights
Summary
This trial will test a computer-based intervention to reduce hazardous drinking among Latinx people with anxiety.
Who is the study for?
This trial is for Latinx individuals aged 21-75 who drink hazardously and have clinical anxiety. Participants must be fluent in Spanish, not currently pregnant, not undergoing psychotherapy for anxiety, and not involved in substance use programs.Check my eligibility
What is being tested?
The study tests a computer-based intervention designed to educate about the risks of alcohol use with anxiety, motivate reduced drinking, and change attitudes towards using alcohol to cope with anxiety among Latinx drinkers.See study design
What are the potential side effects?
Since this is a behavioral intervention involving personalized feedback rather than medication or medical procedures, there are no direct physical side effects expected from participating.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 21 and 75 years old.
Select...
I am between 21 and 75 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently in therapy for anxiety.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline pre pfi completion to 6-months post pfi completion
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline pre pfi completion to 6-months post pfi completion
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Alcohol Attitudes Scale
Modified Drinking Motives Questionnaire-Revised
Motivation to Reduce Alcohol Consumption Scale
Secondary outcome measures
Alcohol Use Disorders Identification Test
Overall Anxiety Severity and Impairment Scale
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Anxiety-alcohol personalized feedback intervention (AA-PFI 2.0)Experimental Treatment1 Intervention
Participants complete the brief (~20-30 minute) AA-PFI 2.0 at baseline.
Group II: Control personalized feedback intervention (C-PFI)Active Control1 Intervention
Participants complete the brief (~20-30 minute) C-PFI at baseline.
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Who is running the clinical trial?
University of HoustonLead Sponsor
148 Previous Clinical Trials
47,348 Total Patients Enrolled
6 Trials studying Anxiety
1,166 Patients Enrolled for Anxiety
National Institute on Alcohol Abuse and Alcoholism (NIAAA)NIH
815 Previous Clinical Trials
1,159,621 Total Patients Enrolled
6 Trials studying Anxiety
3,177 Patients Enrolled for Anxiety
Michael J Zvolensky, Ph.D.Principal InvestigatorUniversity of Houston
5 Previous Clinical Trials
352 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You identify as Latinx or Hispanic.You are currently enrolled in a program for alcohol or substance use.I am between 21 and 75 years old.I am between 21 and 75 years old.I have been diagnosed with clinical anxiety.You are currently drinking alcohol in a dangerous or harmful way.I am currently in therapy for anxiety.I am fluent in Spanish.I am fluent in Spanish.I have been diagnosed with clinical anxiety.You identify yourself as Latinx or Hispanic.You currently drink alcohol in a dangerous or harmful way.
Research Study Groups:
This trial has the following groups:- Group 1: Anxiety-alcohol personalized feedback intervention (AA-PFI 2.0)
- Group 2: Control personalized feedback intervention (C-PFI)
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.
Anxiety Patient Testimony for trial: Trial Name: NCT05246202 — N/A
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