- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07274553
Mindfulness-Based Stress Reduction for Adolescents: Effects on Game Addiction, Stress, and Sleep (MBSR)
December 11, 2025 updated by: Muş Alparslan University
The Effect of a Mindfulness-Based Stress Reduction Program on Digital Game Addiction Levels, Perceived Stress, and Sleep Quality in Adolescents
This randomized controlled trial investigated the impact of a Mindfulness-Based Stress Reduction (MBSR) program on digital game addiction, perceived stress, and sleep quality among adolescents.
The primary research questions were as follows: Does the Mindfulness-Based Stress Reduction Program influence adolescents' levels of digital game addiction?
Does the Mindfulness-Based Stress Reduction Program affect adolescents' perceived stress levels?
Does the Mindfulness-Based Stress Reduction Program impact adolescents' sleep quality?
Participants, aged 12-16, will be randomly allocated to either an intervention group, which will undergo an 8-week MBSR program, or a control group, which will continue with routine school activities.
The MBSR program comprises weekly 40-minute sessions that include breath awareness, body scanning, mindful movement, and emotion regulation exercises.
Data will be collected using the Digital Game Addiction Scale, Perceived Stress Scale, and Pittsburgh Sleep Quality Index at both the pretest and posttest stages.
This study is anticipated to contribute to the development of preventive strategies for behavioral addictions and enhance the emotional well-being and sleep patterns of adolescents.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
The Mindfulness-Based Stress Reduction (MBSR) program is a structured behavioral intervention aimed at enhancing awareness and emotional regulation through mindfulness practices.
This study assessed the efficacy of an 8-week MBSR program implemented in high school settings in Muş, Turkey.
A total of 80 adolescents (40 intervention and 40 control) will voluntarily participate in the study.
The intervention group will engage in mindfulness sessions concentrating on "being present," "breath awareness," "accepting difficult emotions," and "self-compassion."
Each session will have a duration of approximately 40 min per week.
Ethical approval was obtained from the Atatürk University Non-Interventional Clinical Research Ethics Committee (Decision No: 2025/461).
The anticipated findings aim to provide evidence supporting the use of mindfulness-based interventions to enhance adolescent mental health and prevent digital gaming addiction.
Study Type
Interventional
Enrollment (Actual)
80
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
-
-
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Erzurum, Turkey (Türkiye)
- Atatürk University, Health Sciences Institute
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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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Adolescents aged between 12 and 16 years
- Enrolled in a high school under the Muş Provincial Directorate of National Education
- Voluntarily agreed to participate and provided informed consent (along with parental consent)
- Able to attend all eight weeks of the mindfulness sessions
- Sufficient literacy and comprehension to complete self-report questionnaires
Exclusion Criteria:
- Diagnosed psychiatric, neurological, or developmental disorder
- Currently receiving psychological therapy or participating in another behavioral program
- Regular use of medication that affects sleep, mood, or cognitive function
- Absence from more than two MBSR sessions
- Declined or withdrew consent during the study period
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: Experimental: Mindfulness-Based Stress Reduction (MBSR)
Participants in this group will receive an 8-week Mindfulness-Based Stress Reduction (MBSR) program specifically designed for adolescents.
Each session lasts approximately 40 minutes and includes breathing awareness, body scan, mindful movement, and emotional regulation exercises.
The sessions are conducted once a week in a classroom setting by a trained instructor.
Participants are encouraged to practice mindfulness exercises at home between sessions.
|
The intervention consists of an 8-week Mindfulness-Based Stress Reduction (MBSR) program adapted for adolescents.
Each weekly session lasts approximately 40 minutes and is conducted in a classroom setting by a trained instructor.
The program includes breathing awareness, body scan, mindful movement, and emotion regulation exercises.
Participants are encouraged to practice mindfulness at home between sessions using simple guided exercises.
|
|
No Intervention: No Intervention: Control Group
Participants in this group will not receive any mindfulness or behavioral intervention.
They will continue their normal school routine and educational activities during the study period.
After the study concludes, they will be offered a brief introductory mindfulness session as an ethical consideration.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Digital Game Addiction Score
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
|
Measured by the Digital Game Addiction Scale.
Score range: 7 (minimum) to 35 (maximum).
Higher scores indicate worse outcomes, representing higher levels of digital game addiction.
|
Baseline (Week 0) and Post-intervention (Week 8)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Score
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
|
Measured by the Perceived Stress Scale.
Score range: 0 (minimum) to 56 (maximum).
Higher scores indicate worse outcomes, reflecting a higher level of perceived stress.
|
Baseline (Week 0) and Post-intervention (Week 8)
|
|
Sleep Quality Score
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
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Measured by the Pittsburgh Sleep Quality Index.
Score range: 0 (minimum) to 21 (maximum).
Higher scores indicate worse outcomes, representing poorer sleep quality.
|
Baseline (Week 0) and Post-intervention (Week 8)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
November 3, 2025
Primary Completion (Actual)
November 10, 2025
Study Completion (Estimated)
January 20, 2026
Study Registration Dates
First Submitted
November 27, 2025
First Submitted That Met QC Criteria
November 27, 2025
First Posted (Estimated)
December 10, 2025
Study Record Updates
Last Update Posted (Actual)
December 18, 2025
Last Update Submitted That Met QC Criteria
December 11, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- B.30.2.ATA.0.01.00/461
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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