- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07564115
The Effectiveness of 4-STEP-Training Program for Social Media Addiction (4-STEP-TPS) and Psychological Problems Among Adolescence (4-STEP-TPS)
Effectiveness of 4-Step-Training Program for Social Media Addiction(4-STEP-TPS) and Psychological Problems Among Adolescence: A Randomezed Control Trial.
Study Overview
Status
Intervention / Treatment
Detailed Description
The present study focuses on the growing concern of social media addiction among adolescents and its associated psychological consequences. In this research the study will be conducted on adolescents aged 13 to 18 years from selected private schools and colleges. A sample of approximately N=120 participants initially enrolled and will be screened out using standardized criteria, including scores above the cut-off on the Social Networking Addiction Scale and below the cut-off on the Secure Flourish Index. After eligibility assessment and screening based on standardised measure N=80 participants will be randomly assigned to either an experimental group receiving the intervention or a waitlist control group. Data will be collected using validated psychological scales measuring social media addiction, flourishing, anxiety, depression, stress, fatigue, insomnia, family relationships, and academic productivity.
The effectiveness of the intervention will be assessed by comparing pre- and post-intervention outcomes between the two groups using statistical analysis. It is expected that the 4-STEP Training Program will significantly reduce problematic social media use and psychological distress while enhancing emotional regulation, psychological well-being, academic engagement, and overall functioning among adolescents. This study is intended to contribute to the development of practical, structured, and evidence-based interventions for managing social media addiction in youth populations.
To address this growing issue, the study introduces the 4-STEP Training Program, a structured and evidence-based intervention designed to reduce social media addiction and improve psychological functioning. The program integrates four key components: screening and psychoeducation, treatment planning and cognitive-behavioral strategies, effective behavioral management techniques, and relapse prevention. These components aim to help adolescents identify maladaptive thoughts and behaviors related to social media use, develop healthier coping strategies, and build long-term self-regulation skills.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Qasir Abbas Qasir Abbas, PhD Clinical Psychology
- Phone Number: 10245 923337683133
- Email: drqasirabbas@gcuf.edu.pk
Study Contact Backup
- Name: Fazilat mehmood Fazilat mehmood, MS Clinical Psychology
- Email: fazilatmehmood084@gmail.com
Study Locations
-
-
Punjab Province
-
Faisalabad, Punjab Province, Pakistan, 38000
- Government College University Faisalabad
-
Contact:
- Qasir Abbas QasirAbbas, PhD Clinical Psychology
- Phone Number: 10245 923337683133
- Email: drqasirabbas@gcuf.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adolescents aged 13-18 years
- Individuals reporting moderate to high levels of social media addiction (based on standardized scale cut-off, e.g., BSMAS/SNAS)
- Regular social media users with an average daily usage of 4 hours or more
- Willingness to participate with informed consent and parental consent
Exclusion Criteria:
- Adolescents who do not meet the inclusion criteria
- Diagnosed with severe psychiatric disorders (e.g., psychosis, severe depression)
- Currently receiving psychological or psychiatric treatment for addiction-related problems
- Presence of serious physical or neurological conditions
- Individuals who are not regular social media users
- Participants who fail to complete pre-test or post-test assessments
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: 1st Arm ( 1-Experimental)
Participants in the experimental group will receive the 4-STEP Training Program for Social Media Addiction (4-STEP-TPS).
The intervention consists of four sequential phases: (1) screening, assessment, and psychoeducation, (2) treatment conceptualization and planning, (3) effective management strategies including cognitive-behavioral and self-regulation techniques, and (4) relapse prevention.
Each phase includes structured sessions (90 minutes each) delivered over a period of four weeks in an individualized format.
The program aims to reduce social media addiction and improve psychological well-being, sleep patterns, and academic functioning.
|
The 4-STEP Training Program (4-STEP-TPS) is distinguished from existing interventions by its structured, multi-component, and individualized approach specifically designed for adolescent social media addiction.
Unlike traditional interventions that often rely on a single method such as psychoeducation or cognitive-behavioral therapy alone, this program integrates psychoeducation, case conceptualization, cognitive-behavioral techniques, self-regulation strategies, and relapse prevention within a sequential four-step framework.
It is delivered on an individual basis, allowing personalized goal-setting and intervention planning according to each participant's social media use patterns and psychological needs.
Additionally, the program incorporates continuous self-monitoring and behavioral tracking to enhance awareness and control over usage behaviors.
Another key feature is its holistic focus, addressing not only addiction but also related outcomes such as psychological distress, sleep pr
|
|
No Intervention: 2nd Arm ( Waitlist Control Condition )
Participants in the waitlist control group will not receive the intervention during the study period.
They will continue their routine activities without any structured treatment.
However, after completion of the study and post-assessment, they will be offered the 4-STEP Training Program.
This group serves as a comparison to evaluate the effectiveness of the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Networking Addiction Scale (SNAS, Shahnawaz & Rehman, 2020)
Time Frame: At Screening , after 4 weeks, and re-assessment upto 6-months
|
The Social Networking Addiction Scale (SNAS) was developed to measure addiction of all forms of social networking across six-dimensions salience (items 1-4), mood modification (items 5-7), tolerance (items 8-10), withdrawal (items 11-14), conflict (item 1517), and relapse (items 18-21) (Shahnawaz & Rehman, 2020).
The SNAS is a 21-item self-reported scale rated on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).
The score can range from 21 to 147.
Any total score above 84 indicates addiction.
The scale has demonstrated good test-retest reliability (0.88) and good validity, as reported by Shahnawaz and Rehman (2020).
|
At Screening , after 4 weeks, and re-assessment upto 6-months
|
|
Secure Flourish Index (SFI, Weziak-Bialowolska et al., 2017)
Time Frame: At Screening after 4 weeks and reassessment upto 6 months
|
The Secure Flourish Index (SFI) was developed to measure long-term flourishing across 6 domains happiness and life satisfaction (items 1-2), physical and mental health (items 3-4), meaning and purpose (items 5-6), character and virtue (items 7-8), close social relationships (items 9-10), and financial and material stability (items 11-12) (WeziakBialowolska et al., 2017).
It is a self-report scale with 2 items per domain, totaling 12 items, rated on a 0-10 scale.
Total scores range from 0 to 120, with higher scores indicating greater flourishing.
It has an internal consistency of 0.85 and good construct validity (Weziak-Bialowolska et al., 2017).
|
At Screening after 4 weeks and reassessment upto 6 months
|
|
Fatigue Assessment Scale (FAS, Michielsen et al., 2003)
Time Frame: At Screening, after 4, weeks and re-assessment upto 6-months
|
The Fatigue Assessment Scale (FAS) was developed to evaluate the physical and mental symptoms of fatigue (Michielsen et al., 2003).
It is a self-report measure with 10 items rated on a 5-point Likert scale ranging from 1 (never) to 5 (always).
The scale has 2 subscales: mental fatigue, measured by the sum of items 3, 6, 7, 8, and 9, and physical fatigue, measured by the sum of items 1, 2, 4, 5, and 10.
Items 4 and 10 are reverse-scored.
The total scores range from 10 (lowest level of fatigue) to 50 (highest level of fatigue).
The scale has an internal consistency of 0.90 and good validity (Michielsen et al., 2003).
|
At Screening, after 4, weeks and re-assessment upto 6-months
|
|
Insomnia Severity Index (ISI, Bastien et al., 2001)
Time Frame: At Screening , after 4 weeks, and re-assessment upto 6-months
|
The Insomnia Severity Index (ISI) was developed as a screening measure for insomnia as well as an outcome measure in treatment research (Bastien et al., 2001).
It is a self-report measure with 7 items rated on a 5-point Likert scale ranging from 0 to 4. The total score ranges from 0 to 28, with higher scores indicating more severe insomnia symptoms.
Although not validated, the developers suggest cutoff scores to be used for interpretation, with total scores of 0-7 indicating "no clinically significant insomnia," scores between 8-14 indicating "subthreshold insomnia," scores between 15-21 indicating "clinical insomnia (moderate severity)," and scores in the range 22-28 indicating "clinical insomnia (severe)."
The scale has an internal consistency of 0.74 (Bastien et al., 2001).
|
At Screening , after 4 weeks, and re-assessment upto 6-months
|
|
Depression, Anxiety and Stress Scales (DASS, Lovibond & Lovibond, 1995)
Time Frame: At Screening, after 4 week and re-assessment upto 6 months
|
The DASS-21 is the shortened version of the DASS-42 and was designed to measure the symptoms of depression, anxiety, and stress (Lovibond & Lovibond, 1995).
It is a self-report measure with 21 items rated on a 4-point Likert scale (0-3).
Each of the three DASS-21 scales, depression (items 3, 5, 10, 13, 16, 17, 21), anxiety (items 2, 4, 7, 9, 15, 19, 20), and stress (items 1, 6, 8, 11, 12, 14, 18), contains 7 items.
The scale has good internal consistency and construct validity in both clinical and non-clinical samples (Antony et al., 1998).
Scores on the DASS-21 must be multiplied by 2 to obtain the final score.
After obtaining the final score for each depression, anxiety, and stress, the final score is compared to the recommended cut-off scores for severity labels (normal, moderate, severe).
|
At Screening, after 4 week and re-assessment upto 6 months
|
|
The Brief Family Relationship Scale (BFRS, Fok, Allen, Henry, 2014)
Time Frame: After Screening, 4 weeks and re-asessment upto 6 months
|
The Brief Family Relationship Scale (BFRS) was proposed and validated by Fok, Allen, Henry, and the People Awakening Team (2014).
This 16-item instrument was specifically adapted from the Relationship dimension of the original Family Environment Scale (FES) developed by Moos and Moos (1994).
By refining the original 27-item.
By developing a 16-item measure of the relationship dimension, the authors provided a practical and efficient way to assess three core components of family functioning: Cohesion, Expressiveness, and Conflict.
This scale is particularly valued in research involving adolescent populations, as it offers a reliable assessment of the family environment while remaining brief enough for use in large-scale community and clinical studies (Fok et al., 2014; Moos & Moos, 1994).
|
After Screening, 4 weeks and re-asessment upto 6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Qasir Abbas Qasir Abbas, PhD Clinical Psychology, Government College University Faisalabad
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GCUF.FS.TPS
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.
Clinical Trials on 4-STEP-Training Program for Social Media Addiction
-
Government College University FaisalabadActive, not recruitingCognitive Behavior Therapy for Social Media AddictionPakistan
Clinical Trials on 4-STEP-Training Program for Social Media Addiction (4-STEP-TPS)
-
Government College University FaisalabadRecruitingSocial Media AddictionPakistan
-
Xi HuangXiamen University; Yilong People's HospitalRecruitingPostpartum Anxiety | Cesarean Section Wound | Postpartum Depression (PPD) | Breastfeeding Self-EfficacyChina
-
UMC UtrechtNational University Hospital, Singapore; Berry Consultants; University of Pittsburgh... and other collaboratorsRecruitingCommunity-acquired Pneumonia, Influenza, COVID-19United Kingdom, United States, Canada, Australia, Netherlands, Spain, Croatia, Belgium, New Zealand, Ireland, France, Italy, Japan, Slovenia, Colombia, India, Nepal, Pakistan, Portugal, Saudi Arabia, Germany, Israel, Czechia, Estonia, F... and more