RECRUITING

A Mobile Intervention for Black Individuals Who Engage in Hazardous Drinking

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to develop and examine a culturally adapted, mobile health application for the Android and iOS platform. The application uses a 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 Black hazardous drinkers with clinical anxiety.

Official Title

A Mobile-Delivered Personalized Feedback Intervention for Black Individuals Who Engage in Hazardous Drinking

Quick Facts

Study Start:2023-05-15
Study Completion:2024-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06416059

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Being 21 years of age or older
  2. * Self-identifying as Black or African American
  3. * Meeting criteria for current hazardous drinking pattern
  4. * Meeting criteria for clinical anxiety
  5. * Being able to provide written, informed consent
  6. * Owning a smartphone.
  1. * Current participation in alcohol or other substance abuse treatment
  2. * Engaged in psychotherapy for anxiety or depression
  3. * Concurrent use of medication for anxiety or depression
  4. * Being pregnant by self-report
  5. * Residence outside of the United States confirmed via survey geolocation
  6. * Inability to provide a valid United States-issued driver's license or identification card to verify identity.

Contacts and Locations

Study Contact

Brooke Y Redmond, Ph.D.
CONTACT
713-743-8056
restorestudy94@gmail.com
Michael J Zvolensky, Ph.D.
CONTACT
713-743-8595
restorestudy94@gmail.com

Principal Investigator

Michael Zvolensky, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Houston

Study Locations (Sites)

RESTORE Laboratory: Research on Emotion, Substance Treatment Outcomes, and Racial Equity
Houston, Texas, 77204
United States

Collaborators and Investigators

Sponsor: University of Houston

  • Michael Zvolensky, Ph.D., PRINCIPAL_INVESTIGATOR, University of Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-05-15
Study Completion Date2024-08-31

Study Record Updates

Study Start Date2023-05-15
Study Completion Date2024-08-31

Terms related to this study

Keywords Provided by Researchers

  • African American
  • Black
  • Personalized Feedback Intervention

Additional Relevant MeSH Terms

  • Alcohol Abuse
  • Anxiety