Personalized Drinking Feedback Interventions

NCT ID: NCT01211353

Last Updated: 2017-06-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

325 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-01-31

Study Completion Date

2013-02-28

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Alcohol Abuse

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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Personalized Drinking Feedback

Personalized feedback on drinking behaviors

Group Type EXPERIMENTAL

Personalized Drinking Feedback

Intervention Type BEHAVIORAL

Personalized feedback about one's drinking habits

Education-Only

Educational information about alcohol

Group Type ACTIVE_COMPARATOR

Education-Only

Intervention Type BEHAVIORAL

Educational information about alcohol use

Interventions

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Personalized Drinking Feedback

Personalized feedback about one's drinking habits

Intervention Type BEHAVIORAL

Education-Only

Educational information about alcohol use

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* OEF/OIF Veteran

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role collaborator

University of Missouri-Columbia

OTHER

Sponsor Role lead

Responsible Party

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Matthew P. Martens

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mattjew P Martens, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Missouri-Columbia

Locations

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Harry S Truman Memorial VA Medical Center

Columbia, Missouri, United States

Site Status

Countries

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United States

Other Identifiers

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1R21AA020180-01

Identifier Type: NIH

Identifier Source: secondary_id

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1R21AA020180-01

Identifier Type: NIH

Identifier Source: org_study_id

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