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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06454565
Other study ID # CCEE2024
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2023
Est. completion date January 30, 2024

Study information

Verified date June 2024
Source Northeast Normal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 157
Est. completion date January 30, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Tai Chi Exercise
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 Tai Chi practice in each session.
Locked exercise
All participants received a six-month intervention of 45 minutes once a day. All participants performed blocked aerobic exercise.
Multiplayer open exercise
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.
Ta Chi combined with locked exercise
All participants received the intervention for six months, 45 minutes each time, once a day. All participants performed blocked exercise followed by Tai Chi exercises. The schedule was consistent with the Tai Chi group and the Blocked Exercise group.
Taijiquan 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 Tai Chi exercises. The schedule was consistent with the Tai Chi group and the Multiplayer Open Exercise group.

Locations

Country Name City State
China Chinese Center of Exercise Epidemiology Changchun Jilin

Sponsors (1)

Lead Sponsor Collaborator
Northeast Normal University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Using a Jamar hydraulic hand dynamometer to investigate change of handgrip in participants. 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
Primary Using a step test to test participants' aerobic endurance. 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
Primary Using a spirometry tester to investigate changes in pulmonary capacity of the participants. Participants will receive a spirometry test before and after the intervention to assess the change in spirometry from baseline at 6 months. Month 6
Primary The participants' flexibility was tested by seated forward bending. 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
Primary The participants reaction abilities were tested by means of a reaction time tester. 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
Primary The balance ability of the participants was tested through a one-legged standing test. 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
Primary The core strength of the participants was tested through a sit-up test. 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
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