- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02570360
Exercise and Treatment-as-usual in Substance Use Treatment Outcomes
December 13, 2019 updated by: University of Wisconsin, Madison
Comparative Effects of Exercise and Treatment-as-usual on Abstinence, Craving, and the Endocannabinoid System in Substance Users
The research study compares the substance abuse treatment outcomes (e.g., craving, withdrawal symptoms, rates of use, abstinence) of standard intensive outpatient care, with or without an added 6-wk aerobic exercise component.
In addition, certain biomarkers associated with both exercise and substance use (e.g., endocannabinoids and cortisol) will be assessed.
In a rolling admissions format over the course of a year, approximately 36 treatment-seeking substance users who are currently receiving Intensive Outpatient Treatment through a local Alcohol or Other Drug Abuse agency will be randomized to either receive 6 weeks aerobic exercise training in addition to standard care or standard care with 6 weekly laboratory visits to complete questionnaires (18 per group).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
21
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
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Wisconsin
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Madison, Wisconsin, United States, 53706
- University of Wisconsin-Madison
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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
21 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Intact cognitive status and ability to provide informed consent
- ability to read and write in English sufficient to provide consent and complete study questionnaires
- current diagnosis of a single or of multiple substance use disorders
- currently enrolled in an Intensive Outpatient Treatment substance use program
- desire to quit and to seek treatment for substance use
- currently sedentary, not participating in any formal/structured exercise program
Exclusion Criteria:
- a history or present diagnosis of severe depression, psychotic, or bipolar disorder
- presence of cardiac disease or any other medical condition that would make engaging in exercise unsafe
- Undergoing methadone treatment
- chronic conditions such as cancer, diabetes, kidney disease, or autoimmune disorders
- women who are pregnant or planning to become pregnant
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: exercise
Participants will engage in their outpatient treatment program as-usual, but additionally complete 30mins of moderately intense aerobic exercise 3 times per week for 6 weeks.
They will complete 6 weeks of treatment, totaling 18 sessions with exercise.
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The EX participants will engage in supervised, individual treadmill exercise 3xs/wk at the UW Natatorium.
Sessions will consist of a 5-minute warm-up followed by 30 minutes of a moderate to moderately-high intensity exercise and then finish with a 5-minute cool down.
Questionnaires will be completed before and after exercise on a weekly basis.
|
|
Placebo Comparator: treatment-as-usual
Participants will engage in their outpatient treatment program as-usual,but additionally complete 6 weekly, hour-long visits to complete questionnaires.
They will complete 6 weeks of treatment (6 sessions total).
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The control (standard care) participants will come to the UW-Natatorium on a weekly basis to complete questionnaires.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Withdrawal Checklist: Change in physical and psychological withdrawal symptoms over the course of the intervention
Time Frame: up to 6 weeks
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withdrawal symptoms will be assessed using the Withdrawal Checklist which asks participants to rate the severity of a variety physical and psychological symptoms over the past 48 hours.
The total score on the Withdrawal Checklist will be used to provide an overall measured of withdrawal.
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up to 6 weeks
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
change in cortisol concentrations
Time Frame: measured before and after sessions (via saliva swab) during the first, third, and sixth weeks of the 6-week intervention
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measured before and after sessions (via saliva swab) during the first, third, and sixth weeks of the 6-week intervention
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change in endocannabinoid concentrations
Time Frame: measured before and after sessions (via single venipuncture)during the first, third, and sixth weeks of the 6-week intervention
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measured before and after sessions (via single venipuncture)during the first, third, and sixth weeks of the 6-week intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Angelique Brellenthin, MS, UW-Madison
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
September 1, 2015
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
September 1, 2016
Study Registration Dates
First Submitted
September 29, 2015
First Submitted That Met QC Criteria
October 6, 2015
First Posted (Estimate)
October 7, 2015
Study Record Updates
Last Update Posted (Actual)
December 18, 2019
Last Update Submitted That Met QC Criteria
December 13, 2019
Last Verified
December 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015-0710
- A176000 (Other Identifier: UW Madison)
- EDUC\KINESIOLOGY\KINESIO (Other Identifier: UW Madison)
- 1R36DA040140-01 (U.S. NIH Grant/Contract)
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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