Depression
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time frame |
|---|---|
| Complete response rate (QIDS-SR16=5); | — |
Secondary
| Measure | Time 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
Beijing Anding Hospital, Capital Medical University