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SMA-M1 paired transcranial magnetic stimulation to improve motor dysfunction in Parkinson's disease: a single-center, double-blind randomized controlled clinical trial

SMA-M1 paired transcranial magnetic stimulation to improve motor dysfunction in Parkinson's disease: a single-center, double-blind randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083325
Enrollment
Unknown
Registered
2024-04-22
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

parkinson's disease

Interventions

SMA-M1 paired transcranial magnetic stimulation group (paired stimulation group, namely treatment group) :The treatment group received SMA-M1 paired transcranial magnetic stimulation, 5 times a week f
SMA sham-M1 transcranial magnetic stimulation group (conventional treatment group, the control group):The control group received sham-stimulation of SMA and M1 transcranial magnetic stimulation. The s

Sponsors

ShanghaiTongji Hospital (Tongji Hospital of Tongji University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosis of Parkinson's disease with motor symptoms and stable medication treatment; (2) Hoehn-Yahr (H-Y) stage 1 to 4; (3) Age 50-80 years, both genders; (4) Normal cognitive function, able to cooperate with assessment and treatment; (5) Willing to sign written informed consent.

Exclusion criteria

Exclusion criteria: (1) Presence of metal implants within a 20cm range of the stimulation site, including DBS. (2) History of epilepsy or predisposing factors for seizures (such as very low rMT). (3) Currently taking medications or consuming foods that significantly affect the effects of magnetic stimulation (such as phenothiazines, amitriptyline, etc.). (4) Concurrent severe illnesses that may hinder completion of treatment. (5) Special populations such as pregnant or lactating women. (6) Patients with tumors.

Design outcomes

Primary

MeasureTime frame
Unified Parkinson's Disease Rating Scale (UPDRS);

Secondary

MeasureTime frame
Parkinson's Disease Quality of Life Questionnaire (PDQ-39);electromyography;Functional Near Infrared Spectral Brain Imaging (fNIRS);Non-motor Symptom Scale (NMSS);Security Index;

Countries

China

Contacts

Public ContactYuhui Chen

ShanghaiTongji Hospital (Tongji Hospital of Tongji University)

2695952213@qq.com+86 21 6611 1140

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026