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Clinical study of taijiquan training combined with repetitive transcranial magnetic stimulation on depressive symptoms in young patients with subthreshold depression

Clinical study of taijiquan training combined with repetitive transcranial magnetic stimulation on depressive symptoms in young patients with subthreshold depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000160
Enrollment
Unknown
Registered
2024-08-04
Start date
2024-08-10
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

subthreshold depression

Interventions

Tai Chi combined with rTMS group:Tai Chi + rTMS stimulation
Tai Chi combined with sham rTMS group:Tai Chi + sham rTMS stimulation

Sponsors

The Third People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1) Age 19 to 30 years old, gender is not limited; 2) The Center for Epidemiologic Studies Depression Scale (CES-D) score between 16 and 25; 3) Right-handedness; 4) Informed consent and voluntary participation.

Exclusion criteria

Exclusion criteria: 1) Satisfaction of diagnostic criteria for mood disorders, bipolar depressive disorder, psychosis, etc. according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-V) diagnostic criteria; 2) Previous history of major depression, epilepsy or family history of epilepsy, neurodegenerative disease, cerebrovascular disease, neurological disease, history of brain injury, etc; 3) Prior use of psychiatric medications or addiction disorders (e.g., drug abuse, alcoholism, etc.); 4) Presence of metal implants in the body, such as pacemakers, cochlear implants, metal joints, and other ferromagnetic foreign objects, high fever, pregnancy, claustrophobia, and other contraindications to MRI scanning; 5) Patients with severe sleep disorders or severe anxiety disorders. The insomnia severity index (ISI) =22, Hamilton Anxiety Scale (HAMA) score =29; 6) Those who are participating in other clinical trials that affect the evaluation of the results of this study.

Design outcomes

Primary

MeasureTime frame
Patient Health Questionnaire, PHQ-9;

Secondary

MeasureTime frame
Perceived Stress Scale, PSS;Medical Outcomes Study 36-Item Short-Form Health Survey,SF-36;Hamilton Depression Scale,HAMD;Generalized Anxiety Disorder,GAD-7;Snaith-Hamilton pleasure scale, SHAPS;Magnetic Resonance Image;Chinese Affective Scale, CAS;Pittsburgh Sleep Quality Index,PSQI;

Countries

China

Contacts

Public ContactJingsong Wu

Fujian University of Traditional Chinese Medicine

jingsongwu01@163.com+86 136 0980 1214

Outcome results

None listed

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