Heavy Drinking Clinical Trial
— BRAIOfficial title:
Brief Religious Alcohol Intervention
Verified date | August 2020 |
Source | University of Houston |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a trial of a brief alcohol intervention, a brief expressive writing intervention that incorporates religious identity.
Status | Completed |
Enrollment | 203 |
Est. completion date | August 11, 2020 |
Est. primary completion date | August 11, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 29 Years |
Eligibility |
Inclusion Criteria: - 18 to 29 years old - Have had a binge episode (4/5 drinks on one occasion for women/men) at least once in the past month - UH students Exclusion Criteria: - Participants who are currently enrolled in treatment for alcohol or other substances - Participants who have been diagnosed with and/or treated for verbal learning disabilities |
Country | Name | City | State |
---|---|---|---|
United States | University of Houston Psychology Department | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
University of Houston |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in the Timeline Follow-Back one month following the intervention | Participants report number of drinks consumed each day over the last month. | It will be assessed before the intervention and one month following the intervention. | |
Secondary | Chang in the Young Adult Alcohol Consequences Questionnaire one month following the intervention | Participants respond to a list of common consequences of alcohol use indicating whether or not they have experienced them. The scale name is the "Young Adult Alcohol Consequences Questionnaire" (Read, Kahler, Strong, & Colder, 2006). The construct of interest measured by this scale is the alcohol problems experienced by the participant. The total score is used, and the range for the total score is 0 to 48. | It will be assessed before the intervention and one month following the intervention. |
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