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Effects of a Periodic Repetitive Transcranial Magenetic Stimulation in Parkinson Disease

A

Anhui Medical University

Status

Active, not recruiting

Conditions

Parkinson's Disease
Transcranial Magnetic Stimulation

Treatments

Drug: Pharmacotherapy(antiparkinsonian drugs)
Other: transcranial magnetic stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT06365190
AHMU-PD-rTMS

Details and patient eligibility

About

Previous studies have shown that repetitive transcranial magnetic stimulation(rTMS) can improve clinical symptoms of Parkinson's disease(PD). Continuous theta-burst stimulation(cTBS) is a novel rTMS protocol that produces physiological effects b acting on neurons in the brain, which can decrease the excitability of motor system. This study aims to explore the long-term effects of cTBS on improvement of movement symptoms in patients with PD.

Full description

This was a open-label clinical trial to assess the Effects of a Periodic Repetitive Transcranial Magenetic Stimulation in Parkinson Disease.

Participants were randomly assigned to the cTBS group and the control group on a 1:1 basis using age as a stratification factor. In the cTBS group, after baseline assessment, participants received cTBS treatment on the left supplementary motor area(SMA) for 14 days, and symptoms were assessed on the second day after treatment. Ten weeks after completion of assessment, a second cTBS session was performed, with all patients taking stable doses of antiparkinsonian medications. The control group only received drug intervention, and symptom assessment was conducted at weeks 13, 23 , 33 , and 43. To rule out the influence of medication on symptom assessment, all patients stopped taking medication for at least 12 hours before assessment.

Enrollment

47 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meet the Chinese diagnostic criteria for Parkinson's disease (2016 version);
  • Age ≥ 40 years old;
  • Stable use of medication for at least 2 weeks;
  • MMSE score ≧ 24 points;
  • Those who can cooperate to complete the experiment; (6) Those who have not received rTMS treatment in the past.

Exclusion criteria

  • History or clinical symptoms of other serious mental illnesses (such as major depression, psychosis, or obsessive-compulsive disorder);
  • Severe organic brain defects on T1 or T2 images;
  • History or unknown epilepsy Cause of loss of consciousness;
  • Head injury, stroke or other neurological disease;
  • Immovable metal objects on or around the head;
  • History of drug abuse within the past 6 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

47 participants in 2 patient groups

cTBS group
Experimental group
Description:
On the basis of drug treatment, a course of TBS treatment is performed every eight weeks.
Treatment:
Other: transcranial magnetic stimulation
Drug group
Other group
Description:
Take antiparkinsonian medications regularly, with follow-up every 8 weeks including medication guidance and symptom assessment
Treatment:
Drug: Pharmacotherapy(antiparkinsonian drugs)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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