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Effectiveness of A Mindfulness-Based Psychoeducational Intervention on Problematic Smartphone Use, Depressive Symptoms, And Sleep Quality Among Chinese University Students: A Randomized Controlled Trial

Effectiveness of A Mindfulness-Based Psychoeducational Intervention on Problematic Smartphone Use, Depressive Symptoms, And Sleep Quality Among Chinese University Students: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119391
Enrollment
Unknown
Registered
2026-02-26
Start date
2026-03-02
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

problematic smartphone use,depressive symptoms,sleep quality

Interventions

Intervention Group :Eight-week Mindfulness-based Psychoeducational Intervention (once per week)
Active Control Group :Eight-week Digital Well-being Psychoeducational Program (once per week)

Sponsors

North China University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1. Full-time undergraduate students aged 18–25 years (inclusive). 2. Positive screening for problematic smartphone use: a total score meeting the cut-off on the Smartphone Addiction Scale–Short Version (SAS-SV) (men >=31; women >=33). 3. In addition to the above, participants must meet at least one of the following: a Patient Health Questionnaire-9 (PHQ-9) total score of 5–19 (indicating mild to moderately severe depressive symptoms), or a Pittsburgh Sleep Quality Index (PSQI) total score >=6 (indicating poor sleep quality). 4. Provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. A severe mental disorder or an acute episode (e.g., a psychotic disorder or bipolar disorder with manic/hypomanic symptoms) that would interfere with participation; 2. A positive suicide-risk screen, or a PHQ-9 score >= 20; 3. Initiated or discontinued psychotropic medication that may affect mood or sleep within the past 4 weeks (e.g., antidepressants, sedative-hypnotics); 4. Participation in, or plans to participate in, another intervention study or clinical trial during the study period targeting smartphone use, mental health, or related behaviors; 5. Participation in structured mindfulness training within the past 3 months (e.g., MBSR/MBCT or an equivalent-intensity program).

Design outcomes

Primary

MeasureTime frame
Problematic smartphone use severity;

Secondary

MeasureTime frame
Depressive symptoms;Sleep Quality;

Countries

China

Contacts

Public ContactChunjuan Niu

North China University of Science and Technology

niuchunjuan@ncst.edu.cn+86 186 0325 1917

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026