CHIPs or College Health Intervention Projects
The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by University of Wisconsin, Madison.
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
University of Wisconsin, Madison
Collaborator:
Information provided by:
University of Wisconsin, Madison
ClinicalTrials.gov Identifier:
NCT00244049
First received: October 21, 2005
Last updated: March 2, 2009
Last verified: March 2009
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Purpose
The goal of the study is to test the efficacy of brief clinician advice in reducing the frequency of high-risk drinking and alcohol-related harm in a population of college students seeking care at five university health care clinics. High-risk drinking is defined as 1) 8 or more episodes of heavy drinking (5 or more drinks in a row) in the past 28 days for male and female students, and/or 2) 50 drinks for male and 40 drinks for female students in the past 28 days, and/or 3) 15 drinks for male and 12 drinks for female students in the past 7 days, and/or 4) One or more episode(s) of heavy drinking which includes 15 or more drinks in a row.
| Condition | Intervention | Phase |
|---|---|---|
|
Alcohol Abuse |
Behavioral: counseling Other: Brief Intervention |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind (Subject) |
| Official Title: | "Primary Care Alcohol Intervention in College Students" |
Further study details as provided by University of Wisconsin, Madison:
Primary Outcome Measures:
- Reduction in binge/high-risk drinking in college-aged students. [ Time Frame: 6-months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- c) fr. of accidents, d) fr. of campus vandalism and interaction police; e) academic perf; f) fr. of unwanted sex; g) fr. of high-risk sex; h) fr. of physical altercations i) ER visits and hospital days; and j) cost vs. benefit of the intervention. [ Time Frame: 6-months ] [ Designated as safety issue: No ]
| Enrollment: | 1000 |
| Study Start Date: | May 2004 |
| Estimated Study Completion Date: | April 2009 |
| Estimated Primary Completion Date: | April 2009 (Final data collection date for primary outcome measure) |
Intervention Details:
-
Behavioral: counseling
Physicians discussed high-risk/binge drinking with college-aged individuals in a health care setting.
Other: Brief Intervention
Physicians discussed effects of high-risk/binge drinking with college-aged individuals in a health care setting.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- subjects who screen positive for high risk drinking on the Health Screening Survey (HSS) and Baseline interview
Exclusion Criteria:
- Students who will be leaving campus due to graduation or for an extended absence prior to the first face to face intervention Female students who are pregnant at the time of randomization Students who are currently suicidal at the time of the baseline interview Students under 18 years of age Students who drink more than 200 drinks in 28 days (referred for treatment).
Contacts and Locations More Information
No publications provided
| Responsible Party: | Dr. Michael Fleming, MD, Department of Family Medicine |
| ClinicalTrials.gov Identifier: | NCT00244049 History of Changes |
| Other Study ID Numbers: | 1 R01 AA014685-01, 1 R01 AA014685-01 |
| Study First Received: | October 21, 2005 |
| Last Updated: | March 2, 2009 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Alcoholism Alcohol-Related Disorders Substance-Related Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 21, 2013