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Recruiting NCT07153692

NCT07153692 Clinical Efficacy and Mechanism of tDCS for Dysphagia in PD

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Clinical Trial Summary
NCT ID NCT07153692
Status Recruiting
Phase
Sponsor Wang Ping
Condition Parkinson's Disease and Parkinsonism
Study Type INTERVENTIONAL
Enrollment 58 participants
Start Date 2025-07-17
Primary Completion 2029-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 100 Years
Study Type INTERVENTIONAL
Interventions
tDCSConventional Dysphagia Treatmentsham tDCS

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 58 participants in total. It began in 2025-07-17 with a primary completion date of 2029-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to verify transcranial direct current stimulation(tDCS) efficacy for Parkinson's disease (PD)-related dysphagia and its mechanism. Subjects are randomly split into two groups: control (sham tDCS + conventional dysphagia treatment) and experimental (real tDCS + conventional treatment). Assessments will be conducted at baseline, after the completion of intervention, and at the 3-month follow-up. Swallowing function will be evaluated via gold-standard videofluoroscopic swallowing study (VFSS) and scales. Resting-state functional magnetic resonance imaging (rs-fMRI) or functional near-infrared spectroscopy (fNIRS) will be measures for tracking changes in abnormal brain regions/networks. Correlations between swallowing recovery and brain function changes, plus group imaging differences, will reveal tDCS's neurophysiological mechanism.

Eligibility Criteria

Inclusion Criteria: * Meet the Chinese Diagnostic Criteria for Parkinson's Disease (2016) or MDS Diagnostic Criteria for Multiple System Atrophy or Progressive Supranuclear Palsy; * VFSS examination indicates dysphagia; * Mini-Mental State Examination (MMSE) score \>23; * Willing to cooperate with the study and sign the informed consent form; Exclusion Criteria: * Comorbid with other diseases that cause dysphagia; * Comorbid with pneumonia, or severe cardiac/renal insufficiency; * Having metal implants in the body * With cognitive impairment or inability to cooperate.

Contact & Investigator

Central Contact

Ping Wang, MS

✉ wangping6288@zju.edu.cn

📞 15158113194

Principal Investigator

Ping Wang

PRINCIPAL INVESTIGATOR

Second Affiliated Hospital of Zhejiang University School of Medicine

Frequently Asked Questions

Who can join the NCT07153692 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 100 Years, studying Parkinson's Disease and Parkinsonism. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07153692 currently recruiting?

Yes, NCT07153692 is actively recruiting participants. Contact the research team at wangping6288@zju.edu.cn for enrollment information.

Where is the NCT07153692 trial being conducted?

This trial is being conducted at Hangzhou, China.

Who is sponsoring the NCT07153692 clinical trial?

NCT07153692 is sponsored by Wang Ping. The principal investigator is Ping Wang at Second Affiliated Hospital of Zhejiang University School of Medicine. The trial plans to enroll 58 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology