Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

The Effectiveness of 4-STEP-Training Program for Social Media Addiction (4-STEP-TPS) and Psychological Problems Among Adolescence (4-STEP-TPS)

27 aprile 2026 aggiornato da: Qasir Abbas, Government College University Faisalabad

Effectiveness of 4-Step-Training Program for Social Media Addiction(4-STEP-TPS) and Psychological Problems Among Adolescence: A Randomezed Control Trial.

This study evaluates the effectiveness of the 4-STEP Training Program in reducing social media addiction and improving psychological well-being among adolescents. Increasing use of social media has been linked with anxiety, depression, stress, sleep problems, low self-esteem, and reduced academic performance, particularly among adolescents who are more vulnerable to social comparison, fear of missing out, and reliance on online validation. To address this issue, a structured intervention integrating psychoeducation, cognitive-behavioral techniques, and relapse prevention strategies is implemented. The study will involve adolescents aged 13-18 years from private schools and colleges, selected based on standardized cut-off scores for social media addiction and low flourishing. The effectiveness of the program will be assessed by comparing experimental and control groups using validated psychological measures. It is expected that the intervention will significantly reduce social media addiction and psychological distress while improving emotional regulation, flourishing, and academic functioning.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

80

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Qasir Abbas Qasir Abbas, PhD Clinical Psychology
  • Numero di telefono: 10245 923337683133
  • Email: drqasirabbas@gcuf.edu.pk

Backup dei contatti dello studio

Luoghi di studio

  • Pakistan
    • Punjab Province
      • Faisalabad, Punjab Province, Pakistan, 38000
        • Government College University Faisalabad
        • Contatto:
          • Qasir Abbas QasirAbbas, PhD Clinical Psychology
          • Numero di telefono: 10245 923337683133
          • Email: drqasirabbas@gcuf.edu.pk

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto

Accetta volontari sani

Sì

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Comportamentale: 4-STEP-Training Program for Social Media Addiction (4-STEP-TPS)
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
Nessun intervento: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Social Networking Addiction Scale (SNAS, Shahnawaz & Rehman, 2020)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Government College University Faisalabad

Investigatori

  • Investigatore principale: Qasir Abbas Qasir Abbas, PhD Clinical Psychology, Government College University Faisalabad

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

20 maggio 2026

Completamento primario (Stimato)

25 agosto 2026

Completamento dello studio (Stimato)

2 settembre 2026

Date di iscrizione allo studio

Primo inviato

27 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 aprile 2026

Primo Inserito (Effettivo)

4 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • GCUF.FS.TPS

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su 4-STEP-Training Program for Social Media Addiction (4-STEP-TPS)

Cerca prove simili

Sponsor e collaboratori

Condizioni mediche

Interventi farmacologici

CROs by country

CROs in United Kingdom

Condizioni

Malattie rare

Interventi farmacologici

Supplementi dietetici

Sponsor / Collaboratori

Sedi

Sottoscrivi