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Completed

NCT Number: NCT00374153

Southern Methodist Alcohol Research Trial (SMART)

The purpose of this study is to look at the effects of assessment, feedback and motivational interviewing on alcohol consumption among college drinkers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Southern Methodist University, Dallas, Texas, United States

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About this study

Excessive alcohol consumption has been a growing problem at many US colleges. In response, colleges and universities have instituted a range of alcohol intervention and prevention programs for students. Motivational Interviewing (MI) is one brief intervention that has been shown to reduce heavy drinking among college students. To date, all college studies of MI have used a format that includes an assessment and feedback delivered in an MI style. Although this format has considerable empirical support, it remains unclear which of the components is necessary to produce behavior change. This study will evaluate the separate and collective effects of MI and feedback among "binge" drinking college students. Additionally, this study will evaluate the effects of the initial drinking assessment, through including a delayed-assessment control group. After an initial screen, 350 students at Southern Methodist University who report at least one heavy (i.e., "binge") episode during the previous two weeks will be randomized to: (1) MI with feedback, (2) MI without feedback, (3) Mailed feedback only, (4) Assessment only, or (5) Delayed assessment only. MI sessions will be delivered by trained and supervised counselors. Participants will be assessed via a secure Internet site at baseline, 3, 6 and 12 months (12 months only for the Delayed-assessment group), with primary outcome measures including self-reported quantity and frequency of drinking, and drinking-related problems. Since college drinking is associated with substantial negative effects for drinkers, as well as for others, the findings of this study may have significant public health implications in terms of reducing costs, and improving services for students who choose to drink.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must be enrolled in Southern Methodist University.
  • Participants must report one "binge" episode (4 or more drinks in one setting for women, 5 or more drinks in one setting for men) in the past two weeks.
  • Participants must be at least 18 years old.

Exclusion criteria

  • Participants will be excluded if they are not enrolled at Southern Methodist University.
  • Participants will be excluded if they do not report at least one "binge" episode in the past two weeks.
  • Participants will be excluded if they are less than 18 years old.

Treatment and study plan

Feedback

Behavioral

Online personal feedback report

Motivational Interview with Feedback

Behavioral

In-person Motivational Interview with personal feedback report

Motivational interview

Behavioral

In-person Motivational Interview only (without a personal feedback report)

Primary outcomes

  1. Drinks per week

    Time frame: one year

  2. Peak BAC

    Time frame: one year

Secondary outcomes

  1. Alcohol Related Consequences (RAPI)

    Time frame: one year

  2. Interpersonal Violence (CADRI)

    Time frame: one year

  3. Readiness to Change (RTCQ)

    Time frame: one year

  4. Protective Behaviors (PBQ)

    Time frame: one year

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Official study title

Dismantling Motivational Interviewing and Feedback for College Drinkers

Important dates

Study start
2006
Primary completion
2008
Study completion
2009
First posted
Sep 8, 2006
Registry last updated
Mar 10, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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