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NOT YET RECRUITING
NCT07446478
NA

TIS for Improving Cognitive Impairment Associated With Schizophrenia

Sponsor: Central South University

View on ClinicalTrials.gov

Summary

This study aims to evaluate the efficacy and safety of TIS targeting the hippocampus in ameliorating cognitive impairment associated with schizophrenia (CIAS). Participants will receive TIS twice a day for 2 weeks. Their clinical data, including the baseline clinical symptom scale score, cognitive function, and MRI data, will be collected at baseline and at the end of the 2-week intervention.

Official title: Efficacy and Safety of Time Interference Stimulation on Cognitive Impairment Associated With Schizophrenia

Key Details

Gender

All

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2026-03-15

Completion Date

2026-05-15

Last Updated

2026-03-17

Healthy Volunteers

No

Interventions

DEVICE

temporal interference stimulation

TIS will use 2 pairs of electrodes placed according to a 10-10 EEG system and fixed with conductive paste to produce a theta burst stimulation pattern. Electric field modeling will be performed utilizing MRI T1 images to optimize the individualized electrode configuration to generate electric field intensities above 0.4 V/m in the hippocampus of each patient. Each session of stimulation lasts 30 minutes.

Locations (1)

Second Xiangya Hospital, Central South University

Changsha, Hunan, China