- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06468839
The Effect of Addiction Management Model on Digital Addiction and Psychological Resilience in Secondary School Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ankara
-
Çankaya, Ankara, Turkey (Türkiye), 06800
- Senem Çelik Yavuz
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Volunteering to participate in the research Being a 6th-grade student in middle school. Being 11 or 12 age. Being able to read, understand, and speak Turkish fluently. Having no auditory or cognitive impairments that would hinder participation. Scoring 65 or above on the Digital Addiction Scale for Children (DASC).- Having voluntary consent provided by both the student and their legal guardian (parental consent)
Exclusion Criteria:
Scoring below 65 on the Digital Addiction Scale for Children (DASC) during the initial screening
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The Addiction Management Model
The Addiction Management Model consists of 6 sessions and will be applied to the intervention group.
|
The experimental group will implement a addiction management model.This model consisted of structured education on digital addiction combined with Emotional Freedom Techniques (EFT).
The intervention included 6 weekly sessions (each lasting 40 minutes).
|
|
No Intervention: Control Group
Participants only responded to the data collection forms.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Digital Addiction Scale for Children
Time Frame: before the intervention, six weeks after the start of intervention, four weeks after implementation of the intervention
|
The Digital Addiction Scale for Children was developed by Hawi et al. (2019). The Turkish validity and reliability study was conducted by Kaçmaz et al. (2023). The scale was developed in accordance with DSM-5 criteria. The instrument consists of 25 items and two subscales: Intrapersonal (tolerance, withdrawal, mental preoccupation, mood modification) Interpersonal relationships (problems, conflict, lying, substitution, relapse) Each item is rated on a Likert-type scale. Higher scores indicate higher levels of digital addiction symptoms. |
before the intervention, six weeks after the start of intervention, four weeks after implementation of the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child and Adolescent Psychological Resilience Scale (CYRM-12)
Time Frame: before the intervention, six weeks after the start of intervention, one months after implementation of the intervention
|
The Child and Adolescent Psychological Resilience Scale (CYRM-12) is a 12-item self-report instrument derived from the original 28-item version developed by Liebenberg et al. (2012). The short form was developed by Liebenberg et al. (2013). The Turkish adaptation was conducted by Arslan (2015). The scale has a single-factor structure and consists of 12 items. Items are rated on a 5-point Likert-type scale ranging from 1 (does not describe me at all) to 5 (describes me completely). Total scores range from 12 to 60. Higher total scores reflect higher levels of psychological resilience. |
before the intervention, six weeks after the start of intervention, one months after implementation of the intervention
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Daily internet usage time
Time Frame: before the intervention, six weeks after the start of intervention, four weeks after implementation of the intervention
|
Average daily internet usage time is assessed via self-report.
Participants report the estimated number of hours spent using the internet per day.
|
before the intervention, six weeks after the start of intervention, four weeks after implementation of the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Ayfer TEZEL, professor, Ankara University
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
- ANKARAUNIVERSITY-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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