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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06416059
Other study ID # STUDY00004389
Secondary ID R41AA031398
Status Recruiting
Phase N/A
First received
Last updated
Start date May 15, 2023
Est. completion date August 31, 2024

Study information

Verified date June 2024
Source University of Houston
Contact Brooke Y Redmond, Ph.D.
Phone 713-743-8056
Email restorestudy94@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Investigators will develop a culturally adapted, brief, single-session PFI delivered via a mobile health application for the Android and iOS platform through an iterative approach using expert input and semi-structured interview sessions. Next, Black hazardous drinkers with clinical anxiety will assess program navigation and conduct usability testing. Finally, Black hazardous drinkers with clinical anxiety will be recruited to complete the final prototype of the mobile health application in order to evaluate the feasibility, acceptability, and initial effects. Initial screening will be conducted via Zoom; baseline and post-treatment data will be collected via Zoom and 1-week, 1-month, and 3-months follow-up data will be collected remotely.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date August 31, 2024
Est. primary completion date July 31, 2024
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Being 21 years of age or older - Self-identifying as Black or African American - Meeting criteria for current hazardous drinking pattern - Meeting criteria for clinical anxiety - Being able to provide written, informed consent - Owning a smartphone. Exclusion Criteria: - Current participation in alcohol or other substance abuse treatment - Engaged in psychotherapy for anxiety or depression - Concurrent use of medication for anxiety or depression - Being pregnant by self-report - Residence outside of the United States confirmed via survey geolocation - Inability to provide a valid United States-issued driver's license or identification card to verify identity.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mobile Application
The mobile application is a culturally adapted, brief, personalized feedback intervention (PFI) to address alcohol misuse in the context of clinical anxiety,

Locations

Country Name City State
United States RESTORE Laboratory: Research on Emotion, Substance Treatment Outcomes, and Racial Equity Houston Texas

Sponsors (2)

Lead Sponsor Collaborator
University of Houston National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Alcohol Use Disorders Identification Test The Alcohol Use Disorders Identification Test will be used to assess drinking quantity, craving, and related consequences to alcohol use. The 10 items are rated with various Likert-type scales. The measure produces a total score by adding all of the items of the measure with higher scores indicating greater problems with alcohol (possible range 0 to 40). A higher score indicates a worse outcome. Change from Baseline Pre PFI Completion to 3-months Post PFI Completion
Primary Overall Anxiety Severity and Impairment Scale The 5-item Overall Anxiety Severity and Impairment Scale will be used to assess anxiety symptom severity and impairment. Each of the items is rated on a Likert-type scale ranging from 0 to 4. Items are summed to produce a total score (possible range 0 to 20). A higher score indicates a worse outcome. Change from Baseline Pre PFI Completion to 3-months Post PFI Completion
Secondary Motivation to Reduce Alcohol Consumption Scale The 1-item Motivation to Reduce Alcohol Consumption Scale will be used to measure current motivation/intention to reduce alcohol. Participants will be asked to select the statement that best describes their motivation/intention to reduce drinking (e.g., "I really want to cut down on drinking alcohol and intend to in the next month"). Higher scores on this measure indicate greater motivation/intention to reduce alcohol consumption (possible range (0-7). Change from Baseline Pre PFI Completion to 3-months Post PFI Completion
Secondary Modified Drinking Motives Questionnaire-Revised The Modified Drinking Motives Questionnaire-Revised will be used to assess expectancies of drinking. For the current study, the 28-item questionnaire will be used as a measure of expectancies of drinking to reduce/cope with anxiety. The measure utilizes a 5-point Likert scale ranging from 1 (almost never/never) to 5 (almost always/always). Scores are averaged with higher scores indicating greater expectancies of drinking to reduce/cope with anxiety (possible range 1 to 5). Change from Baseline Pre PFI Completion to 3-months Post PFI Completion
Secondary Alcohol Attitudes Scale The 7-item Alcohol Attitudes Scale will be utilized to measure maladaptive attitudes for drinking (e.g., "Drinking alcohol is good"). Items are rated on a Likert-type scale from 1 (strongly disagree) to 7 (strongly agree). Scores will be averaged to create a composite score (possible range 1 to 7). Higher scores indicate greater maladaptive attitudes for drinking. Change from Baseline Pre PFI Completion to 3-months Post PFI Completion
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