Can brain stimulation sharpen Decision-Making in Parkinson's?
NCT ID NCT01845883
First seen Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time
Summary
This study investigates how the brain makes decisions when visual information is uncertain, focusing on the roles of the basal ganglia and cerebellum. Researchers will compare healthy adults with patients who have Parkinson's disease, dystonia, or cerebellar damage, and will test whether deep brain stimulation (DBS) or certain medications affect decision-making performance. Participants perform a visual task while their brain activity is influenced by DBS (on/off) or medication status. The goal is to understand the neural mechanisms behind perceptual choices under uncertainty, which could inform future treatments for these conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Deep Brain Stimulation (DBS) - a procedure that uses implanted electrodes to deliver electrical pulses to specific brain areas.
- What this could lead to
- If successful, this research could clarify how the basal ganglia and cerebellum support decision-making under uncertainty, potentially guiding future treatments for Parkinson's disease, dystonia, and ataxia.
- What could go wrong
- This is an early-stage observational study with a small number of participants, so findings may not apply broadly. DBS carries risks such as infection, bleeding, or device-related complications.
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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.
- Started
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Apr 2013
- Expected to finish
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Dec 2016
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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Accepted
You do not need to have the condition being studied to take part.
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: * Group 1 - Age and Sex matched healthy controls: * Age 18-80 Years Group 2 - Patients with Parkinson's Disease - No DBS: * "on meds" and "off meds" (tested in separate sessions) - total of 2 sessions * Age 45-80 Years * Unified PD rating scale (UPDRS) * Mini mental health Status (MMHS) Group 3 - Patients with Parkinson's Disease already consented for DBS (STN): * Age 45-80 Years * Unified PD rating scale (UPDRS) * Mini mental health Status (MMHS) Group 4 - Patients with Parkinson's Disease already consented for DBS (GPi): * Age 45-80 Years * Unified PD rating scale (UPDRS) * Mini mental health Status (MMHS) Group 5 - Patients with Cervical Dystonia - No DBS * Age 30-80 years * Fahn-Marsden dystonia rating scale (FMDRS) * Mini mental health Status (MMHS) Group 6 - Patients with Generalized Dystonia (Ach) - No DBS: * Age 30-80 years * Fahn-Marsden dystonia rating scale (FMDRS) * Mini mental health Status (MMHS) Group 7 - Patients with Dystonia already consented for DBS (GPi): * Age 30-80 years * Fahn-Marsden dystonia rating scale (FMDRS) * Mini mental health Status (MMHS) Group 8 - Patients Cerebellar Stroke * Age 30-80 Years * Routine neuro exam * Mini mental health Status (MMHS) Group 9 - Patients Cerebellar Ataxia * Age 30-80 Years * Routine neuro exam * Mini mental health Status (MMHS) Exclusion Criteria: * Visual impairment or ocular motility disorder Inability to sit for the 30 minute task plus 20-30 minute instruction time, setup, and wait time. For Group 1 (Age Sex Matched Controls), there will additional exclusion criteria of other neurological disease and drug use
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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
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Neuroscience Research Building
Los Angeles, California, 90095, United States
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Other studies related to the condition(s) this trial covers.
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