Tests aerobic exercise tracked by smart bands for depression
Tests aerobic exercise with smart wristband monitoring in adults with major depressive disorder.
Plain-language title generated from the registry record
Registry title: Individualized Exploration of Aerobic Exercise-assisted Treatment of Depression
Key facts
- Where
- Beijing, ChinaSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 45 years old?
Source: NCT06594588, who can take part
Where in China
- Peking University Sixth HostipalBeijing, ChinaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Peking University
- Trial code
- NCT06594588
- Record updated
- 2 July 2025
- Original description
The goal of this project is to quantify the relative effectiveness of aerobic exercise monitored by smart wristbands in assisting the treatment of depression and improving cognitive function. It aims to explore the mechanisms through which aerobic exercise exerts its effects using imaging genetics and other methods, and to identify suitable populations for exercise, ultimately providing personalized clinical exercise prescriptions. This study will intervene from a behavioral perspective and also seeks to motivate participants to change and improve their physical activity habits.Read full original descriptionShow less
Individualized Exploration of Aerobic Exercise-assisted Treatment of Depression Monitored by Smart Band: a Randomized Controlled Trial
The goal of this project is to quantify the relative effectiveness of aerobic exercise monitored by smart wristbands in assisting the treatment of depression and improving cognitive function. It aims to explore the mechanisms through which aerobic exercise exerts its effects using imaging genetics and other methods, and to identify suitable populations for exercise, ultimately providing personalized clinical exercise prescriptions. This study will intervene from a behavioral perspective and also seeks to motivate participants to change and improve their physical activity habits.
Inclusion: Aged 18-45 years (including 18 and 45), no gender restriction; Meets the diagnostic criteria for depressive disorders according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V); Outpatients or inpatients; Hamilton Depression Rating Scale 17-item (HAMD-17) score ≥ 14; Mood Disorder Questionnaire (MDQ) screening negative to exclude bipolar disorder patients; and Clinical Global Impressions-Severity (CGI-S) score ≥ 4; Maintained on antidepressant treatment for at least 4 weeks or not using antidepressant treatment; Written informed consent obtained from the patient.
Exclusion: Currently undergoing systematic psychological therapy; Diagnosed with other mental disorders, including schizophrenia, bipolar disorder, alcohol or substance abuse/dependence, eating disorders, etc; Individuals with intellectual disabilities or who are unable to cooperate for other reasons, or those lacking or having incomplete civil capacity during the onset of illness; Suffering from neurological or organic brain diseases (such as stroke, cerebral hemorrhage, brain tumors, Parkinson's disease, epilepsy, etc.) and a history of severe traumatic brain injury; Suffering from conditions with high exercise risk, such as hypertension or heart disease; In the 3-minute step test, males with a recovery heart rate more than131 and females with a recovery heart rate more than 140; Physically restricted individuals unable to participate in physical exercise; Physical Activity Readiness Questionnaire (PAR-Q) score ≥ 2; Pregnant women or individuals with contraindications to MRI examinations; Individuals with severe suicidal tendencies or at risk of harming others.