GOALS: Parent Intervention to Reduce Binge Drinking
Sponsor
Penn State University (Other)
Overall Status
Completed
CT.gov ID
NCT01126164
Collaborator
(none)
800
1
3
46
17.4
Study Details
Study Description
Brief Summary
Parent and peer interventions to reduce student drinking
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Detailed Description
Parent and peer interventions to reduce student drinking:
Efficacy;
Mediation:
Moderation
Study Design
Study Type:
Interventional
Actual Enrollment
:
800 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Parent Intervention to Reduce Binge Drinking
Study Start Date
:
Sep 1, 2005
Actual Primary Completion Date
:
Jul 1, 2009
Actual Study Completion Date
:
Jul 1, 2009
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: parent handbook parent handbook |
Behavioral: Parent Handbook and Peer Basics
Parent and Peer delivered interventions
Other Names:
|
Experimental: peer basics peer delivered basics |
Behavioral: Parent Handbook and Peer Basics
Parent and Peer delivered interventions
Other Names:
|
Experimental: parent handbook and peer basics parent handbook and peer basics |
Behavioral: Parent Handbook and Peer Basics
Parent and Peer delivered interventions
Other Names:
|
Outcome Measures
Primary Outcome Measures
- heavy episodic drinking [6 months post baseline]
typical daily drinking
- heavy episodic drinking [9 months post baseline]
typical daily drinking
- heavy episodic peak drinking [6 months post baseline]
peak number of drinks in one night
- heavy episodic peak drinking [9 months post baseline]
peak number of drinks in one night
Secondary Outcome Measures
- drinking consequences [9 months post baseline]
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)
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- varsity athlete in high school
Exclusion Criteria:
- not a varsity athlete in high school
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Penn State University | University Park | Pennsylvania | United States | 16802 |
Sponsors and Collaborators
- Penn State University
Investigators
- Principal Investigator: Robert Turrisi, Ph.D., Penn State University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Robert Turrisi,
Professor of Biobehavioral Health and Prevention Research Center,
Penn State University
ClinicalTrials.gov Identifier:
NCT01126164
Other Study ID Numbers:
- R01AA012529
First Posted:
May 19, 2010
Last Update Posted:
Mar 16, 2021
Last Verified:
Mar 1, 2021
Keywords provided by Robert Turrisi,
Professor of Biobehavioral Health and Prevention Research Center,
Penn State University
Additional relevant MeSH terms: