- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01601743
Exercise as a Behavioral Treatment for Cocaine Dependence
January 26, 2015 updated by: Richard De La Garza, Baylor College of Medicine
The purpose of this study is to test the effects of exercise on cocaine use, fitness, and cravings for cocaine and nicotine.
This study is part of an effort to develop treatments for cocaine abuse.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This proposal represents an important research effort with considerable public health significance in that it will provide detailed behavioral and physiological data for a non-pharmacological intervention to treat stimulant addiction.
Regular exercise is known to promote better mental and physical health, however the effects of exercise on cocaine use and craving in cocaine-dependent individuals has not been previously assessed.
The Specific Aims include: 1) To evaluate the effects of regular exercise (running and walking) versus placebo (sitting) on basic fitness measures; 2) To evaluate the effects of exercise on objective and subjective measures of cocaine and nicotine use and craving.
Participants will also receive a total of 12 sessions of a standardized series of computerized cognitive behavioral therapy (CCBT) modules, which are specifically designed for the treatment of cocaine addiction.
Study Type
Interventional
Enrollment (Actual)
24
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
-
-
Texas
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Houston, Texas, United States, 77030
- Michael E. DeBakey Veterans Affairs Medical Center
-
-
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:
In order to participate in the study, participants must:
- 1. Be English-speaking volunteers between 21-55 years of age
- 2. Be cocaine-dependent and nicotine-dependent (>10 cigarettes/day and FTND >4)
- 3. Be seeking treatment for cocaine dependence
- 4. Have vital signs as follows: resting pulse between 50-90 bpm, supine blood pressures between 85-150 mmHg systolic and 45-90 mmHg diastolic
- 5. Have a breathalyzer test indicating an undetectable blood alcohol level
- 6. Have a medical history and brief physical examination demonstrating no clinically significant contraindications for study participation, in the judgment of the admitting physician and the PI. Most relevant, assessments will include the participants' general health and suitability for inclusion in a rigorous exercise program.
Exclusion Criteria:
Potential participants will be excluded if any of the following apply:
- 1. Have neurological or psychiatric disorders, as assessed by MINI, such as: a. current major depression; b. lifetime history of schizophrenia, other psychotic illness, or bipolar illness; c. current organic brain disease or dementia assessed by clinical interview; d. current psychiatric disorder as assessed by the MINI including history of suicide attempts within the past three months and/or current suicidal ideation/plan
- 2. Meet DSM-IV criteria for abuse or dependence on other drugs, except for cocaine or nicotine
- 3. Have any of the conditions defined by the American College of Sports Medicine (2006) as "absolute contraindications to exercise testing"
- 4. Have evidence of clinically significant heart disease or hypertension
- 5. Have evidence of clinically significant or unstable medical illness including: neuroendocrine, autoimmune, renal, hepatic, or active infectious disease
- 6. Be pregnant or nursing. All females must provide a negative pregnancy urine test
- 7. Currently use alpha or beta agonists, theophylline, or other sympathomimetics
- 8. Currently engaged in an exercise regimen of similar intensity as those planned for investigation
- 9. Have any other illness, condition, or use of medications, which in the opinion of the PI and/or the study physician would preclude safe and/or successful completion of study.
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: Sitting
Sitting for the same period of time and duration (30 minutes per session, 3 times per week, over 4 consecutive weeks).
|
Sitting for the same period of time and duration (30 minutes per session, 3 times per week, over 4 consecutive weeks).
|
|
Active Comparator: Running
Exercise (running) for 30 minutes per session, 3 times per week, over 4 consecutive weeks.
|
Exercise (running) for 30 minutes per session, 3 times per week, over 4 consecutive weeks.
|
|
Active Comparator: Walking
Exercise (walking) for 30 minutes per session, 3 times per week, over 4 consecutive weeks.
|
Exercise (walking) for 30 minutes per session, 3 times per week, over 4 consecutive weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The effects of exercise on cardiovascular and basic fitness measures
Time Frame: 4 weeks
|
Before and after each exercise session, physiologic responses will be closely monitored using repeated HR, BP, and ECG readings.
To evaluate safety, a DSMB will meet annually and following any serious AE to examine data as well as any new published information on exercise relevant to the project.
The number of AEs (including arrhythmias and ECG changes), changes in BP and HR, and changes in mood and psychiatric symptoms (using the BSI, BDI, POMS, and BPRS) will also be assessed throughout the study.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The effects of exercise on changes in drug use measures and in self-reported craving for cocaine and/or nicotine
Time Frame: 4 weeks
|
The effects of exercise (running vs. walking 30 min per session, 3 times per week, over 4 consecutive weeks) versus placebo (sitting for the same period of time and duration) on self-reports of craving for cocaine/nicotine will be measured by the Brief Substance Craving Scale (BSCS), Wisconsin Smoking Withdrawal Scale (WSWS), and the Questionnaire of Smoking Urges (QSU-Brief) throughout the 4-week study period and at 2 follow-up visits.
|
4 weeks
|
|
The effects of exercise on Brain Derived Neurotrophic Factor (BDNF) in blood samples
Time Frame: 4 weeks
|
The effects of exercise versus placebo on changes in BDNF will be measured, since exercise has been shown to increase BDNF and neurogenesis in the hippocampus.
Approximately 2 mls of blood will be taken for BDNF analysis at six timepointss during and after the study: 1) On day 1 prior to randomization 2) once weekly on Fridays - i.e., 4 measures at end of treatment at Week 1, 2, 3, and 4. Samples will be taken 20 minutes before participants run, walk or sit.
3) at follow up visit (39 weeks or 52 weeks).
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4 weeks
|
|
The effects of exercise on changes in drug use measures
Time Frame: 4 weeks
|
The effects of exercise (running vs. walking 30 min per session, 3 times per week, over 4 consecutive weeks) versus placebo (sitting for the same period of time and duration) on changes in drug use will be assessed by measuring urine toxicology and salivary nicotine and cotinine throughout the 4-week study and at 2 follow-up visits.
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Richard De La Garza, II, PhD, Baylor College of Medicine
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, 2011
Primary Completion (Actual)
July 1, 2014
Study Completion (Actual)
July 1, 2014
Study Registration Dates
First Submitted
February 20, 2012
First Submitted That Met QC Criteria
May 16, 2012
First Posted (Estimate)
May 18, 2012
Study Record Updates
Last Update Posted (Estimate)
January 27, 2015
Last Update Submitted That Met QC Criteria
January 26, 2015
Last Verified
May 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-27380
- DPMC (Other Identifier: NIDA)
- 1R21DA030722 (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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