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Digital exercise intervention therapy for residual symptoms of depression:A randomized double-blind controlled trial

Digital exercise intervention therapy for residual symptoms of depression:A randomized double-blind controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084484
Enrollment
Unknown
Registered
2024-05-17
Start date
2024-06-11
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Depression

Interventions

Exercise intervention group:Develop personalized electronic exercise intervention prescriptions
Control group:Regular push of daily activity guidance

Sponsors

Beijing Anding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Outpatient participants, aged 18 to 50 (inclusive), of any gender. 2.Participants with a Visual Analog Scale (VAS) score = 5 after pharmacological treatment (participants perceive a recovery of = 50% compared to pre-treatment). 3.Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR16) score > 5. 4.No regular participation in physical exercise previously (regular physical exercise defined as additional cumulative exercise time of 150 minutes per week, apart from daily activities, for at least 8 weeks). 5.Education level of at least primary school, capable of understanding the content of the scales. 6.Participants must sign an informed consent form themselves.

Exclusion criteria

Exclusion criteria: 1.History of definite manic or hypomanic episodes. 2.Previously diagnosed with bipolar disorder, schizophrenia, schizoaffective disorder, or other psychiatric disorders. 3.History of alcohol or drug dependence and acute intoxication. 4.Pregnant women. 5.Patients deemed to have a significant risk of suicide by the investigator, with a score of 3 or higher on the Suicide item of the Hamilton Depression Rating Scale (HAMD). 6.Undergoing physical therapy, systematic psychotherapy, or other treatments for the current episode. 7.Currently suffering from severe physical illness or physical illness that the investigator considers unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Complete response rate (QIDS-SR16=5);

Secondary

MeasureTime frame
Complete response rate (HAMD-17=7);Quick Assessment Scale for Depressive Symptoms (QIDS-SR16);Hamilton Depression Scale 17 items (HAMD-17);Silhan Disability Scale (SDS);Pittsburgh Sleep Quality Index Scale (PSQI);Fatigue Severity Scale (FSS);Generalized Anxiety Assessment Scale (GAD-7);

Countries

China

Contacts

Public ContactRuinan Li

Beijing Anding Hospital, Capital Medical University

lrn0509@163.com+86 136 8362 2730

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026