Alcohol Consumption Clinical Trial
— GOALSOfficial title:
Parent Intervention to Reduce Binge Drinking
NCT number | NCT01126164 |
Other study ID # | R01AA012529 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2005 |
Est. completion date | July 2009 |
Verified date | March 2021 |
Source | Penn State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Parent and peer interventions to reduce student drinking
Status | Completed |
Enrollment | 800 |
Est. completion date | July 2009 |
Est. primary completion date | July 2009 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 25 Years |
Eligibility | Inclusion Criteria: - varsity athlete in high school Exclusion Criteria: - not a varsity athlete in high school |
Country | Name | City | State |
---|---|---|---|
United States | Penn State University | University Park | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Penn State University |
United States,
Turrisi R, Larimer ME, Mallett KA, Kilmer JR, Ray AE, Mastroleo NR, Geisner IM, Grossbard J, Tollison S, Lostutter TW, Montoya H. A randomized clinical trial evaluating a combined alcohol intervention for high-risk college students. J Stud Alcohol Drugs. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | heavy episodic drinking | typical daily drinking | 6 months post baseline | |
Primary | heavy episodic drinking | typical daily drinking | 9 months post baseline | |
Primary | heavy episodic peak drinking | peak number of drinks in one night | 6 months post baseline | |
Primary | heavy episodic peak drinking | peak number of drinks in one night | 9 months post baseline | |
Secondary | drinking consequences | frequency of blackouts, hangovers, vomiting, fights, unplanned sex, trouble with police, poor academic performance as measured by the rapi; yaapst (standard instruments used in all college alcohol prevention trials) | 9 months post baseline |
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