Can a tuned brain implant sharpen thinking in Parkinson's?
NCT ID NCT06518824
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Many people with Parkinson's disease develop problems with thinking and memory, and few treatments help. This trial tests whether deep brain stimulation delivered at a specific rhythm, called theta frequency, can improve working memory. Participants already have a stimulator implanted in the subthalamic nucleus, a brain region involved in movement and thinking. Researchers turn the device on and off while participants complete a memory task, then compare how well they do.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- theta-frequency deep brain stimulation of the subthalamic nucleus
- What this could lead to
- If it works, theta stimulation could offer a way to ease the thinking and memory problems that often come with Parkinson's disease, using a device many patients already have.
- What could go wrong
- This is a small, early study of 27 people who already have brain stimulators. The approach may not improve thinking, and adjusting stimulation could affect movement control or cause other side effects.
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 27 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Oct 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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18 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: * Those with STN DBS devices * Those with pre- and post-operative imaging * Those that are at least 3 months post-operative Exclusion Criteria: * Those unable to complete the cognitive task (due to language barriers or dementia) * Those with significant DBS complications
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Leslie and Gordan Diamond Health Care Centre
RECRUITINGVancouver, British Columbia, V5Z 1M9, Canada
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