- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04902092
Brain Exercise and Addiction Trial (BEAT)
Brain Exercise and Addiction Trial: Efficacy of a 12-week Aerobic Exercise Regime for Restoring 'Brain Health' in Cannabis Users
Study Overview
Status
Intervention / Treatment
Detailed Description
Heavy cannabis use is associated with substantive learning and memory impairments and elevated risk of psychopathology. It has been repeatedly demonstrated that the hippocampus, centrally implicated in these processes, is particularly vulnerable to the deleterious effects of prolonged exposure to cannabis. This deterioration of hippocampal structure, function, and biochemistry can be reversed, but this requires two or more years of abstinence from cannabis. However, most heavy cannabis users find it extremely difficult to maintain abstinence over extended periods and current treatments for cannabis use disorders are inadequate. There is a pressing clinical need for an intervention that rapidly accelerates hippocampal recovery, ameliorates the associated cognitive impairments and mental health symptoms, and leads to improved treatment outcomes. One promising candidate is physical exercise. In addition to the well-known physical health benefits, regular exercise also has a potent positive effect on brain health and can increase the size of the hippocampus. It's not yet known how much or what kind of exercise produces the best results. This study has been designed to compare the effects of two different exercise programs.
- 12 weeks of regular HIIT exercise
- 12 weeks of regular strength training
The research team are investigating whether the programs have a positive impact on brain health and, if they do, whether one is more effective than the other. The research team will also measure whether engaging in either program leads to a reduction in cannabis consumption, and improvements in thinking skills, mental health, and general wellbeing.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Victoria
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Melbourne, Victoria, Australia, 3800
- Monash University, BrainPark
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 20-55 years
- Voluntary and able to provide informed consent
- Fluent in English
- Current moderate - severe cannabis use disorder
- Major history of cannabis use (i.e. ≥3 days per week on average for ≥4 of the past 6 years)
- Capacity to tolerate physical exercise according to 'Fitness to Exercise'
Exclusion Criteria:
- Have a history of cardiovascular disease, high blood pressure, musculoskeletal injury or other condition that would preclude safe engagement in VO2 max fitness testing and/or regular physical exercise
- Severe claustrophobia, non-MR compatible metallic implant, or other contraindication to MRI scanning
- Lifetime history of significant neurological illness, or moderate - severe brain injury,
- Current major unstable medical illness or chronic pain condition
- Lifetime history of schizophrenia, schizoaffective disorder, OCD, PTSD, bipolar disorder
- Current significant depression or anxiety that precludes ability to reliably engage in the exercise program
- Current moderate - severe substance use disorder for substances other than cannabis (excluding nicotine)
- Currently pregnant or lactating
- Shift work employment schedule within the prior 6-months
- Have engaged in ≥5 sessions of HITT or resistance training within the past 12-months
- History of treatment with antipsychotic medications
- Current participation in psychosocial treatment for substance use disorder
- Other psychoactive medications or psychosocial treatments will be considered on a case-by-case basis. Where a current psychoactive medication is deemed acceptable, both dose and type must have been stable for a minimum of four weeks prior to baseline assessment, and remain stable throughout the 12-week exercise phase of the study.
Study Plan
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 |
---|---|
Active Comparator: High Intensity Physical Training
12-week, 36 session, cardiorespiratory-focussed physical exercise program delivered by an accredited exercise physiologist
|
Exercise sessions will commence with an initial 3-week accustomization period whereby training load will increase incrementally from 2 x 45min sessions with effort peaking at 60% VO2 max (week 1) increasing to 3 x 45minute with effort peaking at 80% VO2max (week 3).
Participants will transition to the full HIIT protocol for the remaining weeks.
The HIIT component will comprise a work-rest ratio of ≥1:1minutes, with alternating exertion epochs at >80% VO2max and <60% VO2max.
As VO2max is likely to increase as fitness improves toward the end of the 3-month program, adjustments to HIIT will be made by the exercise physiologist based on real-time heart rate monitoring, ensuring greater accuracy in participants achieving their heart rate targets.
|
Active Comparator: Low Intensity Physical Training
12- week, 36 session, strength-focussed physical exercise program delivered by an accredited exercise physiologist
|
Exercise sessions will comprise a combination of strength, coordination and mobility exercises.
The strength component will consist of 2-3 sets of resistance exercises at ≤70% of a predicted 1 repetition maximum, targeting all body segments.
Heart rate tracking will occur to ensure participants do not exceed 70% v02 (or exceed Lactate Threshold).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in hippocampal integrity
Time Frame: Baseline (0 months), post (3 months)
|
Composite score derived from three hippocampal health indices: volume (structural MRI), connectivity (DTI), neuronal health (MRS NAA) calculated as described in Yucel et al (2016), doi:10.1038/tp.2015.201.
|
Baseline (0 months), post (3 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in cannabis use
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Time line follow back
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in cannabis dependence
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Severity of Dependence Scale (SDS; range = 0-15 higher scores indicate higher dependence
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in cannabis craving
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Penn Craving Scale (PCS; range = 0 - 30 higher scores indicate greater craving)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in depression symptoms
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Quick Inventory of Depressive Symptomology (QUIDS; range = 0 - 27 higher scores indicate greater depression symptom severity)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in anxiety symptoms
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
StateTrait Anxiety Inventory (STAI; range = 20 to 80, higher scores indicate greater anxiety)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in resilience
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Connor David Resilience Scale (CDRS; range = 0-100 higher scores indicate higher resilience)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in coping skills
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Perceived Stress Scale (10 item; range = 0 - 40 higher scores indicate greater stress)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in sleep quality
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Pittsburgh Sleep Quality Index (PSQI; range = 0 to 21 higher scores indicate worse sleep quality)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in mental wellbeing
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Warwick Edinburgh Mental Wellbeing Scale (WEMWBS; range = 14-70 higher scores indicate increased mental well being)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in quality of life
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Quality of Life and Satisfaction Questionnaire - Short Form (QOL-SF; range = 70 higher scores indicate greater life satisfaction and enjoyment)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in memory
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Rey Auditory Verbal Learning Test (RAVLT)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in associative memory
Time Frame: Baseline (0 months), post (3 months), follow up (6 months)
|
Paired Associates Learning Task (PAL)
|
Baseline (0 months), post (3 months), follow up (6 months)
|
Change in visual memory
Time Frame: Baseline (0 months), post (3 months)
|
Figural Memory Tasks
|
Baseline (0 months), post (3 months)
|
Change in cardiorespiratory fitness
Time Frame: Baseline (0 months), post (3 months)
|
VO2 max
|
Baseline (0 months), post (3 months)
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Murat Yucel, Monash University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 12563
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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