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

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

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.

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

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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