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The efficacy of an online exercise intervention for improving depressive symptoms among patients with subthreshold depression in primary care: a randomized controlled trial

The efficacy of an online exercise intervention for improving depressive symptoms among patients with subthreshold depression in primary care: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087923
Enrollment
Unknown
Registered
2024-08-07
Start date
2024-08-12
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Subthreshold depression

Interventions

"Exercise is Medicine" (EIM) program:12-week EIM class
Control Group:Usual care

Sponsors

Joint Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criteria for this study are 1) aged 18 years or above; 2) screened by the Patient Health Questionnaire depression scale (PHQ-9) with results categorized as subthreshold depression, major depression or no depression.

Exclusion criteria

Exclusion criteria: The exclusion criteria are 1) dysthymia with subthreshold depressive symptoms that last for 2 years or more; 2) major depression within the past 6 months, lifetime history of other psychiatric disorders including generalized anxiety disorder, schizophrenia and bipolar affective disorder, alcohol or substance abuse, presence of serious suicidal risk and medical illness with a prognosis of less than 6 months to live; 3)patients who are taking antidepressants; 4) patient currently enrolled in any form of psychological interventions for any depressive disorders or symptoms and 5) presence of physical conditions and include the presence of recently diagnosed or uncontrolled cardiovascular diseases or uncontrolled hypertension, metabolic, vascular or neurological conditions.

Design outcomes

Primary

MeasureTime frame
Depressive Symptoms;

Secondary

MeasureTime frame
Anxiety Symptoms ;Quality of Life;Physical activity levels ;Medication use and health service utilization ;

Countries

China

Contacts

Public ContactSamuel Yeung-shan WONG

JC School of Public Health and Primary Care, Prince of Wales Hospital, Chinese University of Hong Kong

yeungshanwong@cuhk.edu.hk+852 2252 8774

Outcome results

None listed

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