New hope for swallowing troubles: brain zaps and muscle therapy show promise
NCT ID NCT07152899
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested two non-invasive treatments—brain stimulation (tDCS) and neuromuscular electrical stimulation (NMES)—to help people with swallowing difficulties caused by stroke or Parkinson's disease. A total of 110 adults aged 18 to 85 took part. The goal was to see if these therapies could improve swallowing safety and function, measured by standard scales. The results could lead to better rehabilitation options for these patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial Direct Current Stimulation (tDCS) and Neuromuscular Electrical Stimulation (NMES)
- What this could lead to
- If successful, these treatments could offer a non-invasive way to improve swallowing and reduce choking risk in people with stroke or Parkinson's disease.
- What could go wrong
- This is a completed early-stage study with no phase designation, so results are preliminary. The treatments may not work for everyone, and individual responses can vary.
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
-
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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110 people
The number who actually took part.
- Started
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Jun 2021
- Finished
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May 2025
- 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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18 to 85 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: * Adults aged 18-85 years * Diagnosis of post-stroke or Parkinson's disease-related dysphagia * Dysphagia duration ≥ 2 weeks for post-stroke patients and ≥ 6 months for Parkinson's disease patients * Ability to undergo rehabilitation therapy * Written informed consent obtained Exclusion Criteria: * Severe dysphagia requiring Percutaneous Endoscopic Gastrostomy (PEG) feeding for more than 1 year * Non-neurogenic causes of dysphagia * Contraindications to tDCS or NMES * Cognitive impairment affecting compliance with treatment
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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.
Contacts and locations
Locations
-
Translational Neurophysiology
Pavia, 27100, Italy
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