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Not yet recruitingNCT07457658CBTUpdated Jul 29, 2026

Cognitive Behavioral Therapy for Mobile Phone Addiction in Hospitalized Patients

An interventional study of Cognitive-behavioral therapy and Traditional treatment in the ward in Problematic Use of Mobile Phones, sponsored by Sir Run Run Shaw Hospital. Not yet recruiting at 1 site in China. Open to participants aged 14 Years and older. Per ClinicalTrials.gov, last updated 2026-07-29.

Sponsored by Sir Run Run Shaw Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
14 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Problematic Use of Mobile Phones

Keywords

  • Problematic use of mobile phones
  • cognitive behavioral therapy
  • psychotherapy
03

In context

Lead sponsor

Sir Run Run Shaw Hospital is the lead sponsor of 123 studies on the registry; 64 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
140 participants (estimated)

Study arms

  • Experimental
    CBT Intervention Group

    Besides traditional treatment in the ward, a self-designed self-help manual for mobile phone addiction was distributed, and five psychological interventions were carried out.

    Other: Cognitive-behavioral therapy

  • Other
    Control Group

    Besides traditional treatment in the ward, a self-designed self-help manual for mobile phone addiction was distributed.

    Other: Traditional treatment in the ward

Interventions

  • OtherCognitive-behavioral therapy

    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.

  • OtherTraditional treatment in the ward

    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.

06

What researchers measure

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.

    Time frame: Baseline and Post-intervention (day 5)

Secondary outcomes

  1. Generalized Anxiety Disorder-7 (GAD7)

    The scale consists of 7 items and uses a 4-level scoring system. The higher the total score, the higher the level of anxiety.

    Time frame: Baseline and Post-intervention (day 5)

  2. Pittsburgh Sleep Quality Index (PSQI)

    Used to evaluate the sleep quality over the past month. This scale consists of 19 self-evaluation items and 5 self-evaluation items. Among them, the 19th self-evaluation item and 5 other evaluation items do not participate in scoring. The 18 self-evaluation items participating in the scoring process constitute 7 components, each of which is scored using a 4-point scoring method ranging from 0-3 points. The sum of the scores for each factor is the total PSQI score. A total score greater than 7 indicates the presence of sleep quality issues.

    Time frame: Baseline and Post-intervention (day 5)

  3. IAT Internet Addiction Questionnaire

    The scale consists of 20 items and is rated on a 5-point scale.

    Time frame: Baseline and Post-intervention (day 5)

  4. General Self Efficacy Scale (GSES)

    The scale consists of 10 items and is rated on a 4-point scale.

    Time frame: Baseline and Post-intervention (day 5)

  5. Self Control Strength Scale (SCS)

    The study used the revised Chinese version of the scale. The scale contains 19 items and adopts a 5-point scoring system.

    Time frame: Baseline and Post-intervention (day 5)

  6. Patient Health Questionnaire-9(PHQ-9)

    The scale consists of 9 items and uses a 4-level scoring system. The higher the total score, the greater the individual's depressive mood.

    Time frame: Baseline and Post-intervention (day 5)

  7. The Anhedonia Scale for Adolescents (ASA)

    A Chinese version of 14 items, with a 4-level scoring system.

    Time frame: Baseline and Post-intervention (day 5)

  8. Short Video Addiction Scale

    Used to measure addiction to short videos. Contains 14 items, using a 5-point scoring system.

    Time frame: Baseline and Post-intervention (day 5)

  9. Social Media Barrier Scale (BSMAS)

    Used to measure social media addiction. The scale consists of 6 items and uses a 5-point scoring system.

    Time frame: Baseline and Post-intervention (day 5)

  10. Pressure Perception Scale (PSS-10)

    Used to measure the subjective perceived level of stress. Using 10 item versions with a 5-point rating.

    Time frame: Baseline and Post-intervention (day 5)

  11. Simplified Barratt Impulse Scale (BBIS) in Chinese

    The simplified scale consists of 8 items and uses a 4-point rating system.

    Time frame: Baseline and Post-intervention (day 5)

  12. Happiness Index Scale (WHO-5)

    The scale consists of 5 items and adopts a 6-level scoring system.

    Time frame: Baseline and Post-intervention (day 5)

  13. Severity of Game Addiction (IGDS9)

    The scale consists of 9 items and uses a 5-point scoring system

    Time frame: Baseline and Post-intervention (day 5)

07

Study locations

1 site
  • Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
    Hangzhou, Zhejiang 310000, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07457658
Lead sponsor
Sir Run Run Shaw Hospital
Responsible party
Sponsor
First posted
Mar 9, 2026
Start date
Jun 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Jun 2027 (estimated)
Last update
Jul 29, 2026

Study contacts

Yanhui Liao
Contact
liaoyanhui@zju.edu.cn
+86 18814898844

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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