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RECRUITING
NCT06802952
NA

RTMS for CHR Based on Personalized Targets Using Magnetoencephalography

Sponsor: Shanghai Mental Health Center

View on ClinicalTrials.gov

Summary

This study is an before-after study in the same subject, which enrolled 26 individuals with high-risk psychiatric syndrome (CHR). The target of subjects intervention relies on the results of magnetoencephalography localization. The medication and dosage remain unchanged during the intervention period or not yet taking antipsychotic medication. The investigators assume that the intervention targets for each CHR subject are individualized.

Official title: RTMS for Clinical High-risk Syndrome of Psychosis Based on Personalized Targets Using Magnetoencephalography

Key Details

Gender

All

Age Range

13 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

26

Start Date

2025-02-07

Completion Date

2026-12-31

Last Updated

2025-02-11

Healthy Volunteers

No

Interventions

DEVICE

rTMS

RTMS using pseudo stimulus intervention in weeks 1-2, for a total of 10 days. After resting for 2 weeks, enter the 3-4 weeks of real stimulation, with 5 days of intervention per week for a total of 10 days. Application of rTMS for 1Hz low-frequency intervention, with intervention parameters of 1400 sessions, 100% exercise threshold, and a total of 23 minutes per session. After each target intervention, rest for half an hour to one hour.

Locations (1)

Shanghai Mental Health Center

Shanghai, China