- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01126164
Parent Intervention to Reduce Binge Drinking (GOALS)
March 12, 2021 updated by: Robert Turrisi, Penn State University
Parent and peer interventions to reduce student drinking
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Parent and peer interventions to reduce student drinking:
Efficacy;
Mediation:
Moderation
Study Type
Interventional
Enrollment (Actual)
800
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
University Park, Pennsylvania, United States, 16802
- Penn State University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- varsity athlete in high school
Exclusion Criteria:
- not a varsity athlete in high school
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: parent handbook
|
Parent and Peer delivered interventions
Other Names:
|
|
Experimental: peer basics
peer delivered basics
|
Parent and Peer delivered interventions
Other Names:
|
|
Experimental: parent handbook and peer basics
|
Parent and Peer delivered interventions
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
heavy episodic drinking
Time Frame: 6 months post baseline
|
typical daily drinking
|
6 months post baseline
|
|
heavy episodic drinking
Time Frame: 9 months post baseline
|
typical daily drinking
|
9 months post baseline
|
|
heavy episodic peak drinking
Time Frame: 6 months post baseline
|
peak number of drinks in one night
|
6 months post baseline
|
|
heavy episodic peak drinking
Time Frame: 9 months post baseline
|
peak number of drinks in one night
|
9 months post baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
drinking consequences
Time Frame: 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)
|
9 months post baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2005
Primary Completion (Actual)
July 1, 2009
Study Completion (Actual)
July 1, 2009
Study Registration Dates
First Submitted
May 17, 2010
First Submitted That Met QC Criteria
May 18, 2010
First Posted (Estimate)
May 19, 2010
Study Record Updates
Last Update Posted (Actual)
March 16, 2021
Last Update Submitted That Met QC Criteria
March 12, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01AA012529 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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