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A multicenter randomized controlled clinical trial of the efficacy and safety of physical therapy in patients with mental disorders

A multicenter randomized controlled clinical trial of the efficacy and safety of physical therapy in patients with mental disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001049
Enrollment
Unknown
Registered
2025-05-27
Start date
2024-11-21
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

mentally disturbed

Interventions

Physical therapy group:True stimulation therapy: Patients were randomly assigned to the percutaneous acupoint electrical stimulation group, transcranial alternating current electrical stimulation grou
control group:Pseudo-stimulation therapy: Patients were randomly assigned to the percutaneous acupoint electrical stimulation group transcranial alternating current electrical stimulation group and de

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) 12-85 years of age; (2) meet one of the DSM-V diagnostic criteria for depressive disorder sleep disorder anxiety disorder obsessive-compulsive disorder post-traumatic stress disorder and cognitive disorder; (3) Can understand and read Chinese. (4) The subjects have signed the informed consent

Exclusion criteria

Exclusion criteria: (1) A previous diagnosis of mental retardation or widespread developmental disorder; (2) heart and lung and other important organ diseases epilepsy tic syndrome and other diseases; (3) Implantation of metal and electronic components in the body such as cardiac pacemakers; (4) Clinically significant neurological disease or loss of consciousness for more than 1 hour of brain trauma determined by medical history; (5) Alcohol or drug abuse lasting more than 10 years; (6) can not understand Chinese and can not fully understand the test instructions; (7) Failure to properly understand informed consent.

Design outcomes

Primary

MeasureTime frame
Functional near-infrared spectroscopy;Hamilton Depression Rating Scale (HAMD);Hamilton anxiety scale;

Secondary

MeasureTime frame
Beijing Ageing Brain Rejuvenation Initiative- episodic memory test;Cattell's Sixteen Personality Factors Test;social support revalued scale;Montreal Cognitive Assessment Scale;VAS Pain Score Scale;Digital Symbol Conversion Test;Life Events Scale;Clock Drawing Test;Animal Fluency Test;Mini-Mental State Examination;Pittsburgh Sleep Quality Index;Simplified Coping Style Questionnaire;

Countries

China

Contacts

Public ContactGang Zhu

the First Affiliated Hospital of China Medical University

gzhu@cmu.edu.cn13704006390

Outcome results

None listed

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