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NCT01211353 Clinical Trial

Personalized Drinking Feedback Interventions

Alcohol Abuse Clinical Trial

Official title:
Personalized Drinking Feedback Interventions for OEF/OIF Veterans

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01211353
Other study ID # 1R21AA020180-01
Secondary ID 1R21AA020180-01
Status Completed
Phase N/A
First received September 28, 2010
Last updated June 15, 2017
Start date January 2011
Est. completion date February 2013

Study information
Verified date June 2017
Source University of Missouri-Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this research is to better understand how to reduce hazardous drinking among OEF/OIF veterans by assessing the effectiveness of a low-cost, computer-delivered preventative program.

Description:

Excessive drinking among OEF/OIF veterans represents an important public health problem for both the veterans themselves and those with whom they interact. The objective of this research is to better understand how to reduce hazardous drinking among this group by assessing the effectiveness of a low-cost, computer-delivered preventative program. It is hypothesized that an intervention that provides personalized feedback about drinking behaviors will be more effective than an education-only control condition at reducing alcohol use and negative alcohol-related consequences.

Recruitment information / eligibility
Status Completed
Enrollment 325
Est. completion date February 2013
Est. primary completion date February 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- OEF/OIF Veteran

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Personalized Drinking Feedback
Personalized feedback about one's drinking habits
• Education-Only
Educational information about alcohol use

Locations
Country Name City State
United States Harry S Truman Memorial VA Medical Center Columbia Missouri

Sponsors (2)
Lead Sponsor Collaborator
University of Missouri-Columbia National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Daily Drinking Questionnaire Several quantity/frequency measures of alcohol use Past 30 Days
Secondary Short Inventory of Problems Measures alcohol-related problems Past 6 Months
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