Brief Academic Future Thinking Intervention for College Student Drinkers

February 17, 2020 updated by: Andrew Voss, University of Memphis

Episodic Future Thinking as a Brief Alcohol Intervention for Heavy Drinking College Students: A Pilot Feasibility Study

The present study investigated the feasibility, acceptability, and initial utility of a brief academic goal-relevant episodic future thinking (A-EFT) task among heavy college drinkers.

First, the study attempts to extend the temporal reach of EFT interventions which have demonstrated immediate reductions in discounting, and alcohol demand. The current study utilized a longitudinal design to evaluate whether EFT can change drinking behavior outside the lab in heavy drinking college students. The two-group experimental design included an active control group, weekly booster contact, and 1-month follow-up. Second, this study seeks to investigate whether the process of engaging in EFT is sufficient to produce effects when cues are not presented during the decision-making task. Lastly, this study adds an academic goal-related focus to the EFT task based on previous research indicating that forming meaningful academic goals is protective against drinking and associated problems.

Study Overview

Study Type

Interventional

Enrollment (Actual)

45

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

    • Tennessee
      • Memphis, Tennessee, United States, 38152
        • The University of Memphis

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Full-time Freshman/Sophomore Student
  • 2+ Recent heavy drinking episodes (4/5 standard drinks in one sitting for men/women)

Exclusion Criteria:

  • Current or past substance abuse treatment
  • Current moderate/severe depressive symptoms

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: Episodic Future Thinking
Brief Academic goal related EFT intervention involving desirable outcomes of current academic goals
Active Comparator: Control: Vivid Memory Task
Matched for time control task involving recall of vivid memories of distinct events/actions from a children's story

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Daily Drinking Questionnaire
Time Frame: Baseline
Indicate how many standard drinks were consumed on each day of a "typical week" in the past month
Baseline
Daily Drinking Questionnaire
Time Frame: 1-month post
Indicate how many standard drinks were consumed on each day of a "typical week" in the past month
1-month post
Alcohol-Related Consequences
Time Frame: Baseline
Young Adult Alcohol Consequences Questionnaire - Indicate "yes" or "no" to experiencing each alcohol-related consequences in the past month
Baseline
Alcohol-Related Consequences
Time Frame: 1-month post
Young Adult Alcohol Consequences Questionnaire - Indicate "yes" or "no" to experiencing each alcohol-related consequences in the past month
1-month post
Alcohol Demand
Time Frame: Baseline
Alcohol Purchase Task - Indicate hypothetical alcohol purchase behavior at a variety of price points
Baseline
Alcohol Demand
Time Frame: Post-session - immediately after intervention;control
Alcohol Purchase Task - Indicate hypothetical alcohol purchase behavior at a variety of price points
Post-session - immediately after intervention;control
Alcohol Demand
Time Frame: 1-month post
Alcohol Purchase Task - Indicate hypothetical alcohol purchase behavior at a variety of price points
1-month post
Delayed Reward Discounting
Time Frame: Baseline
5-Choice Minute Discounting task - Indicate preference for various choices of immediate small vs. larger delayed rewards
Baseline
Delayed Reward Discounting
Time Frame: Post-session - immediately after intervention/control
5-Choice Minute Discounting task - Indicate preference for various choices of immediate small vs. larger delayed rewards
Post-session - immediately after intervention/control
Delayed Reward Discounting
Time Frame: 1-month post
5-Choice Minute Discounting task - Indicate preference for various choices of immediate small vs. larger delayed rewards
1-month post

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Protective Behavioral Strategies
Time Frame: Baseline
Indicate frequency of use of each protective strategy on a 1-6 Likert-type scale (1 = Never, 6 = Always)
Baseline
Protective Behavioral Strategies
Time Frame: 1-month post
Indicate frequency of use of each protective strategy on a 1-6 Likert-type scale (1 = Never, 6 = Always)
1-month post
Academic Engagement
Time Frame: Baseline
Single item assessing time spent studying during the past week
Baseline
Academic Engagement
Time Frame: 1-month post
Single item assessing time spent studying during the past week
1-month post

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

January 20, 2018

Primary Completion (Actual)

August 30, 2019

Study Completion (Actual)

August 30, 2019

Study Registration Dates

First Submitted

February 5, 2020

First Submitted That Met QC Criteria

February 17, 2020

First Posted (Actual)

February 19, 2020

Study Record Updates

Last Update Posted (Actual)

February 19, 2020

Last Update Submitted That Met QC Criteria

February 17, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • PRO-FY2017-587

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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