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A Study on the Effectiveness of Rest Shame Interventions Based on Cognitive Behavioural Therapy in Reducing Social Media Addiction

NCT07284160 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-01-01
Last updated
2025-12-16

Condition(s) studied

Rest is Shameful

Investigational drug(s) / intervention(s)

Structured intervention based on cognitive behavioural therapy (CBT)

Structured intervention based on cognitive behavioural therapy (CBT): Structured intervention based on cognitive behavioural therapy (CBT)

Study summary

This study will employ a randomised controlled trial design to systematically intervene in university students' rest shaming through a structured intervention programme grounded in cognitive behavioural therapy (CBT), thereby examining its efficacy in reducing social media addiction. Through this research, we aim to evaluate the effectiveness of CBT interventions in alleviating rest shaming and demonstrate that operationalising rest shaming influences social media addiction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
Accepted
Inclusion Criteria: * University students aged 18-25 who are capable of understanding and completing research-related tasks, and who have confirmed the presence of rest shaming experiences via the Rest Shaming Scale. Exclusion Criteria: * Individuals with a history of severe mental illness (such as clinically diagnosed depression, anxiety disorders, etc.), cognitive impairment, or an inability to cooperate in completing the research process.

Primary outcome measure(s)

  • rest intolerance scale — From enrollment to the end of treatment at 1 week
  • Social media addiction — From enrollment to the end of treatment at 1 week

Trial sites (1)

FacilityCityRegionStatus
The Fourth Affiliated Hospital of Zhejiang University School of Medicine Yiwu Zhejiang
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07284160 on ClinicalTrials.gov ↗ ← All trials in China