Purpose

The purpose of this study is to develop, evaluate the acceptability/feasibility (Phase IA), and test (Phase IB) the effectiveness of a brief, integrated, single-session, computer-based, culturally adapted personalized feedback intervention (PFI) designed to enhance knowledge regarding adverse anxiety-alcohol interrelations, increase motivation and intention to reduce hazardous drinking, and reduce positive attitudes and intention regarding anxiety-related alcohol use among Latinx hazardous drinkers with anxiety.

Conditions

Eligibility

Eligible Ages
Between 21 Years and 75 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Being between the age of 21 to 75 years of age - Being self-identified as Latinx or Hispanic - Fluent in Spanish - Meeting criteria for current hazardous drinking pattern - Meeting criteria for clinical anxiety - Being able to provide written, informed consent

Exclusion Criteria

  • Being involved in alcohol or other substance use program - Currently pregnant - Current engagement in psychotherapy for anxiety

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Anxiety-alcohol personalized feedback intervention (AA-PFI 2.0)
Participants complete the brief (~20-30 minute) AA-PFI 2.0 at baseline.
  • Behavioral: Alcohol-Anxiety Personalized Feedback Intervention 2.0
    AA-PFI 2.0 is a culturally adapted, brief, computer-delivered, personalized feedback intervention to address alcohol misuse in the context of clinical anxiety.
    Other names:
    • AA-PFI 2.0
Active Comparator
Control personalized feedback intervention (C-PFI)
Participants complete the brief (~20-30 minute) C-PFI at baseline.
  • Behavioral: Control Personalized Feedback Intervention
    C-PFI is a brief, computer-delivered, personalized feedback intervention on exercise and nutrition.
    Other names:
    • C-PFI

Recruiting Locations

More Details

Status
Recruiting
Sponsor
University of Houston

Study Contact

Brooke Y Kauffman, Ph.D.
713-743-8056
bkauffma@central.uh.edu

Detailed Description

In the first phase, the investigators will collect qualitative and quantitative feedback from focus groups to refine intervention content and evaluate treatment acceptability and feasibility of a novel, brief, integrated, culturally adapted computer-based personalized feedback intervention (PFI). In the second phase, Latinx hazardous drinkers with clinical anxiety will be recruited and randomly assigned to either the refined culturally adapted anxiety-alcohol PFI (AA-PFI 2.0) or a control PFI (C-PFI). Initial screening will be conducted via telephone; baseline and post-treatment data will be collected in-person; and 1-, 3-, and 6-month follow-up data will be collected online remotely.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.