A Study on the Effectiveness of Rest Shame Interventions Based on Cognitive Behavioural Therapy in Reducing Social Media Addiction
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Structured intervention based on cognitive behavioural therapy (CBT).
- Who it may be relevant to
- Registry conditions: Rest is Shameful. Basic parameters: 18 years — 25 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Other Structured intervention based on cognitive behavioural therapy (CBT)
Structured intervention based on cognitive behavioural therapy (CBT)
Primary outcome measures
- rest intolerance scale [Time frame: From enrollment to the end of treatment at 1 week]
- Social media addiction [Time frame: From enrollment to the end of treatment at 1 week]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Health services research
Study locations
China · 1 center
- The Fourth Affiliated Hospital of Zhejiang University School of Medicine — Yiwu
Identifiers
NCT: NCT07284160 · KY-2025-286