Zapping the brain without surgery: a new hope for Parkinson's?
NCT ID NCT07698236
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study tests a noninvasive technique called temporal interference stimulation (TIS) to see if it can improve motor symptoms in people with Parkinson's disease and related conditions. Participants receive both active and sham stimulation in a random order, with each session lasting 30 minutes over three days. The main goal is to measure changes in movement scores using a standard rating scale. If successful, TIS could offer a safer alternative to implanted deep brain stimulators.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Temporal Interference Stimulation (TIS) device
- What this could lead to
- If effective, this could offer a noninvasive way to improve motor symptoms in Parkinson's disease, potentially reducing the need for invasive deep brain stimulation surgery.
- What could go wrong
- This is an early-stage crossover study with only 100 participants. The effects may be modest or not last, and individual responses can vary. Risks include discomfort from stimulation and the possibility that sham stimulation may also show some benefit.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Aged 40 to 80 years, diagnosed with idiopathic Parkinson's disease or Parkinsonian syndromes according to the Movement Disorder Society (MDS) diagnostic criteria. 2. Receiving stable doses of levodopa or other dopaminergic medications for at least 4 weeks prior to enrollment, with a documented response to levodopa; medication regimen must remain unchanged during the study. 3. Hoehn and Yahr (H\&Y) stage ≤ 3 in the "ON" medication state. 4. Normal cognitive function, defined as a Mini-Mental State Examination (MMSE) score ≥ 24. 5. Able to maintain and cooperate with Parkinson's disease symptom diaries. 6. Signed written informed consent. Exclusion Criteria: 1. Presence of other neurological or psychiatric disorders that may interfere with study participation or outcomes. 2. Previous treatment with deep brain stimulation (DBS) or other invasive brain stimulation therapies. 3. Orthopedic or other medical conditions that could affect gait or balance. 4. Contraindications to MRI, such as claustrophobia or other factors making MRI unsuitable. 5. History of taking antipsychotic, antidepressant, or other medications that may affect dopamine levels. 6. Contraindications to electrical stimulation, such as implanted cardiac pacemakers or a history of epilepsy. 7. History of electroconvulsive therapy (ECT). 8. Severe comorbidities, including cardiovascular disease, respiratory disease, or hepatic/renal dysfunction.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Shanghai Jiao Tong University School of Medicine Affiliated Ruijin Hospital
Shanghai, China
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Other studies related to the condition(s) this trial covers.
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