CClinicalTrials.gg
RecruitingNCT07091292ExIT-CUpdated Jul 29, 2025

Exercise Intervention as Treatment for People Using Cannabis (ExIT-C)

An interventional study of Indoor Cycling and Indoor Cycling in Cannabis Abuse, Cannabis Dependence and Cannabis Use Disorder, sponsored by The University of Hong Kong. Recruiting at 1 site in Hong Kong. Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-07-29.

Sponsored by The University of Hong Kong · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2025; still recruiting 1 year 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

In Hong Kong, although the total number of drug abusers is trending down in recent years, the number of cannabis users continues to surge. The misuse of cannabis, if left unattended, predisposes various degrees of dependence and use disorders, which could later on induce psychotic disorders and schizophrenia. Effective strategies combating cannabis dependence and cannabis use disorder (CUD) are therefore warranted.

Exercise presents as a low-cost and low-stigma alternative to traditional pharmacotherapy and psychotherapy in the treatment of substance use disorders, which also promotes physical well-being with virtually no side effects. While exercise has some success in treating use disorders of stimulants, alcohol, and tobacco, evidence of its effects on CUD remains scarce. Hence, the present study will be conducted to assess the effectiveness of a 12-week aerobic exercise training regimen on reducing cannabis dependence and the severity of CUD.

Participants with cannabis dependence will be randomly assigned to either the exercise or the control group. Participants assigned to the exercise group will partake in a 12-week aerobic exercise training program of vigorous-intensity using indoor bikes, whereas those assigned to the control group will perform sham exercise of very light-intensity on indoor bikes. The 12-week study is divided into three (3) 4-week phases:

  1. Intensive Intervention - all participants will exercise twice a week under supervision.
  2. Active Intervention - all participants will exercise once a week under supervision.
  3. Passive Maintenance - no supervised exercise sessions will be provided. All participants will receive exercise reminders via weekly text messages.

Cannabis use-related, cognitive, and physical outcomes will be assessed every 4 weeks, whereas withdrawal symptoms will be assessed and urine quick test administered every week.

02

Conditions studied

  • Cannabis Abuse
  • Cannabis Dependence
  • Cannabis Use Disorder

Keywords

  • exercise
  • cannabis
  • cannabis use disorder
  • cannabis dependence
  • substance abuse
03

In context

Marijuana Abuse

517 studies on the registry are indexed under Marijuana Abuse; 114 are open to participants now.

This study's planned enrollment of 60 is close to the median of 60 across 421 interventional studies indexed under Marijuana Abuse.

Browse Marijuana Abuse studies →

Lead sponsor

The University of Hong Kong is the lead sponsor of 1,262 studies on the registry; 340 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Young adults of 18-40 years old
  • Able to read and communicate in English and/or Chinese
  • Able to give informed consent
  • Using cannabis or marijuana as the primary psychoactive substance of abuse
  • Suffering from cannabis addiction, defined by:

    i. Cannabis Dependence with an SDS score ≥ 3, or ii. Cannabis Use Disorder according to the Diagnostic and Statistical Manual of Mental Disorders 5th Edition (DSM-5), or iii. Cannabis Harmful Use or Dependence according to the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) or Clinical descriptions and diagnostic requirements for International Classification of Diseases 11th Revision (ICD-11) mental, behavioral, and neurodevelopmental disorders.

Exclusion criteria

Exclusion Criteria:

  • Age \< 18 or > 40 years old
  • Unable to read English or Chinese
  • Unable to give informed consent
  • Absolute and/or relative contraindications to exercise training as indicated by the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) and the electronic Physical Activity Readiness Medical Examination (ePARmed-X+)
  • Had been diagnosed with the following disorders, including:

    i. Neurodevelopmental Disorders DSM-5: Intellectual Disabilities, Communication Disorders, Specific Learning Disorder, Autism Spectrum Disorder and Motor Disorders ICD-11: Disorders of intellectual development (6A00), Developmental speech or language disorders (6A01), Autism spectrum disorder (6A02), Developmental learning disorder (6A03), Developmental motor coordination disorder (6A04), Stereotyped movement disorder (6A06), Primary tics or tic disorders (8A05.0) ii. Other DSM-5 defined Substance Use Disorder greater than mild in severity (i.e., severity score ≥ 2), except for tobacco or caffeine iii. Neurocognitive Disorders (DSM-5, or ICD-11 6D70-72 \& 6D80-86)

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Exercise Intervention Treatment (ExIT) Group

    Behavioral: Indoor Cycling

  • Sham comparator
    Sham-exercise Control (SCN) Group

    Behavioral: Indoor Cycling

Interventions

  • BehavioralIndoor Cycling

    Indoor cycling at 60-70% HR reserve for 30 minutes.

  • BehavioralIndoor Cycling

    Indoor cycling at 20-30% HR reserve for 30 minutes.

06

What researchers measure

Primary outcomes

  1. Clinical Diagnosis of Cannabis Use Disorder (CUD)

    Structured Clinical Interview for DSM-5 Disorders (SCID-5) is used to ascertain the diagnosis and severity of CUD

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  2. Psychological Dependence on Cannabis

    Severity of Dependence Scale (SDS) is used to assess psychological dependence on cannabis

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

Secondary outcomes

  1. Urine Toxicology Test

    Drug of Abuse Urine Test Kits is used to ascertain recent use of cannabis and/or other substances

    Time frame: At enrollment and 1, 2, 3, 4, 5, 6, 7, 8, and 12 weeks after enrollment

  2. Cannabis Craving

    Marijuana Craving Questionnaire - Short Form (MCQ-SF) is used to assess cannabis craving

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  3. Cannabis Problems

    Cannabis Problems Questionnaire (CPQ) is used to assess cannabis-related problems

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  4. Cannabis Withdrawal

    Cannabis Withdrawal Scale (CWS) is used to assess cannabis withdrawal symptoms

    Time frame: At enrollment and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 weeks after enrollment

  5. Self-Efficacy in Cannabis Use Reduction

    Marijuana Reduction Strategies Self-Efficacy Scale (MRSSES) is used to assess self-efficacy in reducing cannabis use

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  6. Self-reported Substance Use History

    The frequency and amount of cannabis and substance use in the past 30 days is recorded

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  7. Global Cognitive Function

    Montreal Cognitive Assessment - HK version (MoCA-HK) is used to assess global cognitive function

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  8. Psychomotor Speed

    Digit Symbol Substitution Test (DSST) is used to assess psychomotor speed

    Time frame: At enrollment and 1, 2, 3, 4, 5, 6, 7, 8, and 12 weeks after enrollment

  9. Body weight (in kg)

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  10. Height (in cm)

    Time frame: At enrollment

  11. Waist circumference (in cm)

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  12. Cardiopulmonary Capacity

    Maximal oxygen uptake (V̇O2max) is measured to assess cardiopulmonary capacity

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  13. Resting Energy Expenditure

    Time frame: At enrollment and 4, 8, and 12 weeks after enrollment

  14. Self-reported Physical Activity Participation

    International Physical Activity Questionnaire - Short Form (IPAQ-SF) is used to record the 7-day physical activity participation

    Time frame: At enrollment and 9, 10, 11, and 12 weeks after enrollment

07

Study locations

1 of 1 sites recruiting
  • Queen Mary Hospital
    Hong Kong, Hong Kong
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07091292
Lead sponsor
The University of Hong Kong
Responsible party
Sponsor
First posted
Jul 29, 2025
Start date
Jul 2, 2025
Primary completion
Dec 2028 (estimated)
Completion
Dec 2028 (estimated)
Last update
Jul 29, 2025

Study contacts

Albert KK Chung, MBBS(HK)
Contact
chungkka@hku.hk
+852-2255-4486

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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