Cognitive Behavioral Therapy for Mobile Phone Addiction in Hospitalized Patients
CBT
The Efficacy of Cognitive Behavioral Therapy for Mobile Phone Addiction and Emotional Improvement in Hospitalized Patients: A Randomized Controlled Trial
2 other identifiers
interventional
140
1 country
1
Brief Summary
Problematic mobile phone use is excessive dependence and use of electronic products and their functions, which affects the daily life of users. Previous studies have shown that mobile phone addiction is related to depression, anxiety severity, and stress, and it is negatively correlated with sleep quality. For hospitalized patients in the mental health department, symptoms such as anxiety, depression, and poor sleep are very common. Cognitive behavioral therapy has been widely applied in online gaming addiction and is also effective in intervening in mobile phone addiction. Therefore, Hospitalized patients in the mental health department will be randomized to either the CBT interventions or an control group. The main outcome measure is the Simplified Smartphone Addiction Scale (SAS-SV), measured before intervention and after the completion of the last brief intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 25, 2026
CompletedFirst Posted
Study publicly available on registry
March 9, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2027
July 29, 2026
February 1, 2026
6 months
February 25, 2026
July 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Simplified version of the Smartphone Addiction Scale (SAS-SV)
The SAS-SV scale was developed by Min Kwon et al. in 2013, consisting of 10 items, and using a 6-level scoring method.
Baseline and Post-intervention (day 5)
Secondary Outcomes (13)
Generalized Anxiety Disorder-7 (GAD7)
Baseline and Post-intervention (day 5)
Pittsburgh Sleep Quality Index (PSQI)
Baseline and Post-intervention (day 5)
IAT Internet Addiction Questionnaire
Baseline and Post-intervention (day 5)
General Self Efficacy Scale (GSES)
Baseline and Post-intervention (day 5)
Self Control Strength Scale (SCS)
Baseline and Post-intervention (day 5)
- +8 more secondary outcomes
Study Arms (2)
CBT Intervention Group
EXPERIMENTALBesides traditional treatment in the ward, a self-designed self-help manual for mobile phone addiction was distributed, and five psychological interventions were carried out.
Control Group
OTHERBesides traditional treatment in the ward, a self-designed self-help manual for mobile phone addiction was distributed.
Interventions
5 CBT intervention: the first intervention was conducted after the patient was hospitalized, completed relevant informed consent and pre-test, and lasted for about 30 minutes once; Follow up intervention 4 times: once a day for about 20 minutes. Traditional treatment in the ward includes drug therapy based on the different conditions of hospitalized patients, physical therapy such as work entertainment, Morita, biofeedback therapy, etc. Some patients may also receive transcranial magnetic stimulation therapy and psychological therapy.
Traditional treatment in the ward includes drug therapy based on the different conditions of hospitalized patients, physical therapy such as work entertainment, Morita, biofeedback therapy, etc. Some patients may also receive transcranial magnetic stimulation therapy and psychological therapy.
Eligibility Criteria
You may qualify if:
- Age ≥ 14 years old.
- Willingness to treat problematic mobile phone usage behavior.
- Voluntarily participate in this study and sign an informed consent form. If the subject is unable to read and sign the informed consent form due to reasons such as lack of legal capacity, or if the subject is a minor, their guardian must act as a proxy for the informed process and sign the informed consent form. If the subject lacks the ability to read the informed consent form (such as illiterate subjects), a witness must witness the informed process and sign the informed consent form.
You may not qualify if:
- Having serious physical or mental illnesses (such as ongoing psychotic symptoms, manic episodes, or severely disabling neurological and psychiatric disorders), unable to cooperate with intervention.
- Previously received or currently undergoing CBT intervention for mobile phone addiction.
- Cognitive impairment patients, critically ill patients, pregnant women, etc.
- There are other situations that researchers consider unsuitable to participate in this study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310000, China
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 25, 2026
First Posted
March 9, 2026
Study Start
June 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
June 1, 2027
Last Updated
July 29, 2026
Record last verified: 2026-02