Alcohol & Exercise Study

NCT ID: NCT05955911

Last Updated: 2025-07-20

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

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-01

Study Completion Date

2025-07-14

Brief Summary

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The goal of this clinical trial is to learn if exercise can reduce alcohol craving in heavy social alcohol drinkers. The main questions this project aims to answer are 1) compared to a distraction activity (i.e., coloring), will mild-to-moderate intensity exercise (i.e., walking on a treadmill) reduce alcohol craving; 2) compared to a distraction, will mild-to-moderate intensity exercise reduce the amount of consumption of an alcohol-placebo beverage.

Detailed Description

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Upon arriving to the study, participants will complete baseline measures assessing for the inclusion and exclusion criteria, as well as baseline alcohol craving and subjective response measures. Participants will then be randomly assigned into the active treatment (exercise) or distraction (coloring) condition. After randomization, participants will consume a low-dose alcohol beverage (BAC=0.03g/dL; equivalent to approximately 1 standard alcohol beverage) within five minutes to induce active alcohol craving. 15 minutes post-beverage consumption, participants will complete the alcohol craving and subjective response measures. At 20 minutes post-beverage consumption, participants will begin their randomly assigned 20-minute activity (exercise or coloring). At approximately 12 minutes into the activity (32 minutes post beverage consumption) and immediately after the activity (44 minutes post beverage consumption), the participants will complete the alcohol craving and subjective response measures. Participants will then be given a tray of three 8oz. cups of water and 3 8oz. cups of an alcohol-placebo beverage and will be allowed to drink as much or as little of the beverages as they would like.

Conditions

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Alcohol-Related Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Exercise

Moderate intensity treadmill walking (40%-59% of heartrate reserve).

Group Type EXPERIMENTAL

Exercise

Intervention Type BEHAVIORAL

20 minutes of Moderate intensity (40%-59% heartrate reserve) walking on a treadmill.

Coloring

Coloring in an adult coloring book as a distraction activity

Group Type OTHER

Coloring

Intervention Type BEHAVIORAL

20 minutes of coloring in adult coloring book

Interventions

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Exercise

20 minutes of Moderate intensity (40%-59% heartrate reserve) walking on a treadmill.

Intervention Type BEHAVIORAL

Coloring

20 minutes of coloring in adult coloring book

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Heavy social alcohol drinkers (i.e., alcohol drinkers who consume 10-40 standard alcohol beverages per week and participate in 1-5 binge drinking episodes \[consume 4+/5+ drinks in a sitting for women/men, respectively\]) per week.

Exclusion Criteria

* Meets DSM-5 diagnostic criteria for a current moderate or severe alcohol use disorder
* Meets DSM-5 diagnostic criteria for a current Moderate or Severe cannabis use disorder
* Endorses daily smoking of tobacco
* Endorses having a current DSM-5 psychiatric disorder
* Endorses having any medical conditions that may interfere with the exercise condition (e.g., knee-replacement, sprained ankle, etc.)
* Has a current level of physical activity that exceeds 20 minutes of moderate-to-vigorous physical activity per day
* Endorses illicit substance use (i.e., use of illicit substances x\>2 times in the past year)
* Has self-reported allergies to pineapple juice, cranberry juice, orange juice, \&/or tonic water
* Individuals not proficient in reading, writing, or speaking in English
* Women who are trying to conceive or who are pregnant
* Women who are currently breastfeeding
Minimum Eligible Age

19 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Western University, Canada

OTHER

Sponsor Role lead

Responsible Party

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Jesus Chavarria

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jesus Chavarria, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Western University

Locations

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Western University

London, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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0000055296

Identifier Type: -

Identifier Source: org_study_id

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