- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06454565
Effects of Traditional Martial Arts, Open and Locked Exercise on the Physical and Mental Health of Drug Users
July 9, 2024 updated by: Guang Yang, Prof. Dr., Northeast Normal University
The aim of this study is to discuss the efficacy of Chinese traditional martial arts in reducing drug addiction and improving the physical and mental health of drug addicts.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
- Behavioral: Locked exercise
- Behavioral: Multiplayer open exercise
- Behavioral: Health Qigong - 12-Step Daoyin Health Preservation Exercises
- Behavioral: Health Qigong - 12-Step Daoyin Health Preservation Exercises combined with locked exercise
- Behavioral: Health Qigong - 12-Step Daoyin Health Preservation Exercises combined with open exercise
Study Type
Interventional
Enrollment (Actual)
189
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
-
-
Jilin
-
Changchun, Jilin, China, 130024
- Chinese Center of Exercise Epidemiology
-
-
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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Normal mental state, able to understand and accept instructions
- Drug users who have survived the detoxification period
- Without major diseases
Exclusion Criteria:
- Drug use for more than 2 years
- Drug abusers who have entered a drug rehabilitation center more than once
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Locked exercise
All classes are held offline with professional instructors.
|
All participants received a six-month intervention of 45 minutes once a day.
All participants performed blocked aerobic exercise.
|
|
Experimental: Multiplayer open exercise
All classes are held offline with professional instructors.
|
All participants received a six-month intervention in the form of a balloon game competition.
The intervention consisted of two phases: the first month consisted of a movement learning and consolidation phase of 45 minutes per session, once a day; the second five months consisted of a formal competition phase of 45 minutes per session, once a day.
In the first phase, coaches taught participants the technical movements and rules.
In the second phase, participants competed in groups during each session, with the coaches acting as referees.
|
|
No Intervention: Control group
Disseminating knowledge about the dangers of drugs
|
|
|
Experimental: Health Qigong - 12-Step Daoyin Health Preservation Exercises
All classes are conducted offline and are implemented by professional Health Qigong instructors.
|
All participants received a six-month intervention consisting of two phases: the first month was a movement learning and consolidation phase of 45 minutes per session, once a day; the second five months were a formal practice phase of 45 minutes per session, once a day.
In the first phase, participants learn four new movements per session and consolidate these exercises in the next session.
After learning all the movements, the remaining time of the first phase was used to consolidate the exercises.
In the second phase, participants perform a full Health Qigong - 12-Step Daoyin Health Preservation Exercises practice in each session.
|
|
Experimental: Health Qigong - 12-Step Daoyin Health Preservation Exercises combined with locked exercise
All classes are held offline with professional instructors.
|
All participants received the intervention for six months, 45 minutes each time, once a day.
All participants performed blocked exercise followed by Health Qigong - 12-Step Daoyin Health Preservation Exercises.
The schedule was consistent with the Health Qigong - 12-Step Daoyin Health Preservation Exercises group and the Blocked Exercise group.
|
|
Experimental: Health Qigong - 12-Step Daoyin Health Preservation Exercises combined with open exercise
All classes are held offline with professional instructors.
|
Behavioral: Health Qigong - 12-Step Daoyin Health Preservation Exercises combined with open exercise
All participants received the intervention for six months, 45 minutes each time, once a day.
All participants performed multiplayer Open Exercise followed by Health Qigong - 12-Step Daoyin Health Preservation Exercises exercises.
The schedule was consistent with the Health Qigong - 12-Step Daoyin Health Preservation Exercises group and the Multiplayer Open Exercise group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Using a Jamar hydraulic hand dynamometer to investigate change of handgrip in participants.
Time Frame: Month 6
|
Participants will receive a handgrip strength test before and after the intervention to assess the change from baseline handgrip strength at 6 months.
|
Month 6
|
|
Using a step test to test participants' aerobic endurance.
Time Frame: Month 6
|
Participants will undergo an aerobic endurance test before and after the intervention to assess the change in aerobic endurance from baseline at 6 months.
|
Month 6
|
|
The participants' flexibility was tested by seated forward bending.
Time Frame: Month 6
|
Participants will receive a seated forward bend test before and after the intervention to assess changes in flexibility from baseline at 6 months.
|
Month 6
|
|
The participants reaction abilities were tested by means of a reaction time tester.
Time Frame: Month 6
|
Participants will receive a response time test before and after the intervention to assess the change in responsiveness from baseline at 6 months.
|
Month 6
|
|
The balance ability of the participants was tested through a one-legged standing test.
Time Frame: Month 6
|
Participants will receive a one-legged standing test before and after the intervention to assess the change in balance from baseline at 6 months.
|
Month 6
|
|
The core strength of the participants was tested through a sit-up test.
Time Frame: Month 6
|
Participants will undergo a sit-up test before and after the intervention to assess changes in core strength from baseline at 6 months.
|
Month 6
|
|
Using a spirometry tester to investigate changes in pulmonary capacity of the participants.
Time Frame: Month 6
|
Participants will receive a spirometry test (vital capacity, ml) before and after the intervention to assess the change in spirometry from baseline at 6 months.
|
Month 6
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
July 1, 2023
Primary Completion (Actual)
December 30, 2023
Study Completion (Actual)
January 30, 2024
Study Registration Dates
First Submitted
June 6, 2024
First Submitted That Met QC Criteria
June 6, 2024
First Posted (Actual)
June 12, 2024
Study Record Updates
Last Update Posted (Actual)
July 11, 2024
Last Update Submitted That Met QC Criteria
July 9, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CCEE2024
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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