- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06837649
The Effect of Mindfulness-Based Tai Chi Chuan on Mobile Phone Addiction Among Male College Students is Associated With Executive Functions
The goal of this clinical trial is to investigate whether an 8-week mindfulness-based Tai Chi intervention can improve cognitive and executive functions, particularly inhibitory control, and reduce mobile phone addiction in male university students. It will also explore the potential mechanisms by which mindfulness-based Tai Chi affects mobile phone addiction behaviors. The main questions it aims to answer are:
Does mindfulness-based Tai Chi improve inhibitory control and reduce mobile phone addiction in male university students? Does mindfulness-based Tai Chi enhance overall executive functions, including inhibition, updating, and shifting abilities? Researchers will compare the experimental group (receiving mindfulness-based Tai Chi intervention) to the control group (maintaining their usual routine without intervention) to see if mindfulness-based Tai Chi leads to greater improvements in cognitive and executive functions and reduces mobile phone addiction.
Participants will:
Practice mindfulness-based Tai Chi for 8 weeks Complete pre- and post-intervention assessments of mobile phone addiction, mindfulness levels, and executive function Engage in weekly Tai Chi practice sessions Complete self-report diaries of mobile phone usage and mindfulness experiences
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100080
- Capital University Of Physical Education And Sports, School of Kinesiology and Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male university students not majoring in physical education. Aged 18 years or older. A moderate level of dependence on mobile phones, with a score above 40 on the Mobile Phone Addiction Index (MPAI).
No regular exercise habits in daily academic life. Willing to participate in an 8-week mindfulness-based Tai Chi training program and provide informed consent.
No serious medical conditions.
Exclusion Criteria:
- The exclusion criteria include individuals with diseases that may affect training (such as cardiovascular diseases, respiratory diseases, and musculoskeletal disorders), as well as those diagnosed with mental disorders (such as depression, anxiety, obsessive-compulsive disorder, etc.).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
The exercise time lasts 40 min each time, including 5 min of wuji pile practice with positive thoughts, 30 min of eight styles of Tai Chi Chuan practice (4 min*6 sets, 1 min interval between sets), and 5 min of relaxation part of wuji pile with music.
The exercise frequency is 3 times a week.
|
Studies have shown that compared with the Tai Chi Chuan, MTCC is more relaxing to practitioner.
The Tai Chi Chuan section is based on the Yang's movements, which not only conform to the basic technical characteristics, such as the steps, stance, techniques, movement of the center of gravity, and the coordination of the whole body between the movements, but also are clear, smooth, simple, easy to learn, and beautiful.
The mindfulness section is complemented by soothing, soft music to guide the practitioner to focus on himself and return to inner peace.
The essence of the program is to help practitioners focus their attention and achieve inner peace during practice.
Through the practice of MTCC, practitioners are encouraged to face the difficulties they encounter in reality and to develop a positive and open mind to deal with negative emotions and thoughts in daily life.
|
|
No Intervention: Control group
The control group maintained their normal physical activity levels without any additional intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mobile Phone Addiction Index
Time Frame: From enrollment to the end of treatment at 8 weeks.
|
Measurement of mobile phone addiction used the Mobile Phone Addiction Index (MPAI) developed by Y.K. Leung, which is suitable for measuring mobile phone addiction in college students with a good reliability of 0.87.
There are four dimensions in the scale, namely loss of control, withdrawal, avoidance, and ineffectiveness.
It is rated from 1 to 5 with 17 questions.
|
From enrollment to the end of treatment at 8 weeks.
|
|
Mindfulness level
Time Frame: From enrollment to the end of treatment at 8 weeks.
|
The Mindful Attention Awareness Scale (MAAS) was used to measure the mindfulness level.
It developed by Brown and Ryan in 2003, which was introduced and revised by domestic scholars in 2012.
Besides, it has high validity, structure validity and retest reliability of 0.87 0.89.
The scale of single dimension scale, score from 1 to 6 points, are all positive ratings, which includes 15 problem.
The higher the total score is, the higher levels one's mindful awareness and attention are.
|
From enrollment to the end of treatment at 8 weeks.
|
|
Executive Functions
Time Frame: From enrollment to the end of treatment at 8 weeks.
|
Executive function was measured by the executive function test instrument developed by Chen Aiguo, whose reliability has been tested in numerous studies.
The test consisted of a Flanker task (inhibition function), a 2-back task (updating function), and a More-odd shifting task (shifting function).
|
From enrollment to the end of treatment at 8 weeks.
|
Collaborators and Investigators
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
- KM202210029001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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