Behavioral activation program for college freshmen to reduce alcohol use
A Cluster-randomized Trial of a Behavioral Activation Intervention Administered in a College Freshman Orientation Course
This study tests a new program for college freshmen that helps them manage stress and sleep better to see if it can also reduce their drinking habits.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Enrollment | 540 (estimated) |
| Ages | 17 Years and up |
| Sex | All |
| Sponsor | University of Kansas Academic / other |
| Locations | 1 site (Lawrence, Kansas) |
| Trial ID | NCT04038190 on ClinicalTrials.gov |
What this trial studies
This intervention focuses on college freshmen during their transition from high school, a critical period for increased alcohol use. It aims to engage students in a behavioral activation program integrated into their freshman orientation course, addressing their primary concerns such as stress and sleep, while indirectly reducing risky drinking behaviors. By encouraging students to set personal goals and participate in reinforcing activities, the program seeks to enhance their overall well-being and reduce alcohol-related problems. The study will evaluate the effectiveness of this approach compared to traditional methods that directly target alcohol consumption.
Who should consider this trial
Good fit: Ideal candidates for this study are college freshmen enrolled in UNIV 101 seminar courses at the University of Kansas.
Not a fit: Patients who are not college freshmen or those not enrolled in the specified seminar courses may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce alcohol-related problems among college freshmen by addressing their broader concerns.
How similar studies have performed: Previous studies have shown promise for behavioral activation approaches in reducing substance use, indicating potential success for this novel application in a college setting.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * College freshmen enrolled in UNIV 101 freshman seminar courses at the University of Kansas assigned to the study Exclusion Criteria: * None
Where this trial is running
Lawrence, Kansas
- University of Kansas — Lawrence, Kansas, United States (Recruiting)
Study contacts
- Principal investigator: Tera L Fazzino, PhD — University of Kansas
- Study coordinator: Tera L Fazzino, PhD
- Email: tfazzino@ku.edu
- Phone: 7858640062
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.