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

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.
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.

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

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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