Status:
NOT_YET_RECRUITING
Combined Exercise and PMS: Impact on Biopsychosocial Function in Older Adults With Schizophrenia
Lead Sponsor:
Yuntong Zhang
Conditions:
Schizophrenia Patients
Eligibility:
All Genders
60-80 years
Phase:
NA
Brief Summary
This project consists of two randomized parallel - group experiments targeting older adults with schizophrenia, aiming to evaluate the therapeutic effect of Peripheral Magnetic Stimulation (PMS). Exp...
Detailed Description
Project Experimental Protocol (Revised Version) This project consists of two randomized parallel-group experiments involving older adults with schizophrenia, aiming to evaluate the therapeutic effects...
Eligibility Criteria
Inclusion
- \# Eligibility Criteria
- Participants must be aged ≥60 years.
- Diagnosis of schizophrenia based on the International Classification of Diseases - 10th Edition (ICD-10) or Diagnostic and Statistical Manual of Mental Disorders - 5th Edition (DSM-5).
- Diagnosis must be made for ≥6 months, with clinical manifestations of schizophrenia (e.g., hallucinations, delusions, thought disorder, etc.).
- No history of severe acute psychiatric episodes or hospitalizations within the last 3 months prior to enrollment.
- Symptoms must be controllable, with no reliance on acute psychiatric intervention.
- Participants must be able to understand the study's purpose and procedures and provide written informed consent. If the participant is unable to provide full informed consent (e.g., due to severe cognitive impairment), informed consent must be obtained from a legal guardian.
Exclusion
- Schizoaffective disorder or bipolar disorder with psychosis.
- Elderly individuals with multiple chronic diseases but who still maintain good functional status and quality of life.
- Presence of severe cardiovascular diseases, liver or kidney dysfunction, cerebrovascular diseases, or other physical conditions that may affect treatment.
- Patients with contraindications to peripheral magnetic stimulation (PMS) treatment or EEG.
Key Trial Info
Start Date :
September 28 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 5 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT07194460
Start Date
September 28 2025
End Date
December 5 2025
Last Update
September 26 2025
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