- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06921096
Cessation on Internet Addiction in College Students (IAD)
April 8, 2025 updated by: Cheng Liang, Chengdu Sport University
Effect of Tai Chi Exercise and Its Cessation on Internet Addiction in College Students: A Randomized Controlled Trial
This study aimed to explore the intervention effect of Tai Chi exercise on internet addiction in college students and its maintenance effect after cessation, providing a scientific basis for the application of Tai Chi in internet addiction intervention among college students.
Fifty-one non-sports-major college students with mild or moderate internet addiction were randomly divided into a Tai Chi group (n = 23) and a control group (n = 24).
The Tai Chi group underwent 12 weeks of Tai Chi exercise, while the control group maintained their regular study schedule without additional physical exercise.
The Chinese Internet Addiction Scale and serum dopamine and β-Endorphin levels were assessed at baseline, week 12, and week 16.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
51
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 Contact
- Name: Hanyu Li
- Phone Number: +8618280314728
- Email: hanyuli_cdsu@163.com
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
Yes
Description
Inclusion Criteria:
- Participants aged 18-25;
- CIAS scores of 26-53 (low internet dependence), 54-80 (moderate dependence), or 81-104 (high dependence). Only mild and moderate cases were included;
- non-sports majors; the study followed the Declaration of Helsinki, and all participants understood the purpose and signed consent forms.
Exclusion Criteria:
- Severe IAD (CIAS score >80);
- Tai Chi practice within 6 months;
- regular exercise habits;
- history of depression/anxiety or undergoing psychological treatment;
- use of medications affecting mental state or neurotransmitter levels.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Maintain your original lifestyle without engaging in regular physical exercise.
Participants were contacted every two weeks via WeChat or in person to monitor their conditions and ensure no extra exercise or medication use.
|
|
|
Experimental: Tai Chi group
The Tai Chi group practiced 24-form simplified Tai Chi for 12 weeks, 3 times/week, 60 minutes/session (including 5-minute warm-up and 5-minute cool-down) at our university's track, under professional coaching, from 8:00-9:10 AM.
The first 4 weeks were for learning, and the next 8 for consolidation.
Then, we will observe all participants for an additional 4 weeks (Week 16) as a follow-up.
|
The Tai chi group practiced 24-form simplified Tai Chi for 12 weeks, 3 times/week, 60 minutes/session (including 5-minute warm-up and 5-minute cool-down) at our university's track, under professional coaching, from 8:00-9:10 AM.
The first 4 weeks were for learning, and the next 8 for consolidation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internet Addiction Scale Survey
Time Frame: 16 weeks
|
The CIAS, tailored to Chinese college students' psychological traits, was used.
It has 26 items across five dimensions: compulsive symptoms, withdrawal symptoms, tolerance symptoms, interpersonal and health problems, and time management problems.
It's a 4-point self-report Likert scale (1="extremely disagree" to 4="extremely agree").
The scale has good reliability and validity, with factor consistency coefficients of 0.70-0.82
and internal consistency of 0.9446[21].
The total CIAS score is the sum of all items, with higher scores indicating greater dependence and addiction risk.
The CIAS was administered at baseline, week 12, and week 16 for both groups.
|
16 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum Dopamine
Time Frame: 16 weeks
|
At baseline, week 12, and week 16, 2 ml of fasting venous blood was collected from participants between 7:00-8:00 AM.
Serum dopamine levels was measured using radioimmunoassay on a Beckman DXC800 autoanalyzer, with reagents from IBL (Germany).
All steps followed the kit instructions, and absorbance was measured at 450 nm to calculate concentrations.
|
16 weeks
|
|
Serum β-Endorphin
Time Frame: 16 weeks
|
At baseline, week 12, and week 16, 2 ml of fasting venous blood was collected from participants between 7:00-8:00 AM.
Serum β-Endorphin levels was measured using radioimmunoassay on a Beckman DXC800 autoanalyzer, with reagents from IBL (Germany).
All steps followed the kit instructions, and absorbance was measured at 450 nm to calculate concentrations.
|
16 weeks
|
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 (Estimated)
April 15, 2025
Primary Completion (Estimated)
August 15, 2025
Study Completion (Estimated)
August 16, 2025
Study Registration Dates
First Submitted
March 29, 2025
First Submitted That Met QC Criteria
April 8, 2025
First Posted (Actual)
April 10, 2025
Study Record Updates
Last Update Posted (Actual)
April 10, 2025
Last Update Submitted That Met QC Criteria
April 8, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Internet Addiction Disorder
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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