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Study identifier: NCT07323602 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors

Condition: Dystonia  ·  Sponsor: Ruijin Hospital

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

This study aims to investigate whether preoperative gait characteristics, measured by wearable sensors, can predict the clinical outcomes of Deep Brain Stimulation (DBS) in patients with dystonia. Participants scheduled for DBS surgery will undergo gait analysis using wearable sensors before the procedure. Clinical assessments, including the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) and the SF-36 Health Survey, will be conducted preoperatively and postoperatively to evaluate surgical efficacy and quality of life. The study seeks to identify gait biomarkers that correlate with optimal DBS response.

This description comes directly from the study's public registry record.

Talk to the study team

Li  ·  +0086-021-64370045  ·  ldy11483@rjh.com.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of MedicineShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07323602