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RecruitingNCT06848530Updated Jul 14, 2026

Neurophysiology of the Basal Ganglia, Thalamus, and Cerebellum in Patients With Movement Disorders

An interventional study of Prescribed Medications and Deep brain stimulation adjustment in Movement Disorders, sponsored by University of Pennsylvania. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-14.

Sponsored by University of Pennsylvania · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Started Dec 2025; still recruiting 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The research study is being conducted to better understand parts of the human brain called the cortex, basal ganglia, thalamus, and cerebellum in patients with movement disorders (such as Parkinson's disease, essential tremor, dystonia, or ataxia). These brain structures are involved in movement disorders. This study attempts to better understand the brain electrical activity associated with these disorders, both in patients with and without deep brain stimulation (DBS). Recordings are made from the scalp with a noninvasive electrode and/or through the DBS stimulator if the participant has a stimulator model that is able to sense brain activity. These recordings are analyzed along with measures of movement disorder symptoms to identify brain signal signatures of symptoms.

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Conditions studied

  • Movement Disorders

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In context

Movement Disorders

371 studies on the registry are indexed under Movement Disorders; 102 are open to participants now.

This study's planned enrollment of 100 is above the median of 46 across 221 interventional studies indexed under Movement Disorders.

Browse Movement Disorders studies →

Lead sponsor

University of Pennsylvania is the lead sponsor of 1,668 studies on the registry; 235 are open to participants now.

Of its 158 completed or terminated interventional studies of FDA-regulated products, 109 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients 18 years of age and above
  • Any patient who has been diagnosed by a movement disorders neurologist with one of the following movement disorders:
  • Parkinson's disease
  • Dystonia
  • Tremor, including essential tremor
  • Cerebellar ataxia
  • Other hyperkinetic movement disorders, such as chorea and tics

Exclusion criteria

Exclusion Criteria:

- Patients with dementia

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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Participants without Deep Brain Stimulators

    Multimodal neurophysiology (for example, electroencephalography and electromyography) will be measured during the following: Movement disorder medication administration -The patient's movement disorders medications, prescribed by their treating physicians outside of this study, may be administered during an experimental session.

    Other: Prescribed Medications

  • Experimental
    Participants with Deep Brain Stimulators

    Multimodal neurophysiology (for example, electroencephalography and electromyography) will be measured during the following: Movement disorder medication administration -The patient's movement disorders medications, prescribed by their treating physicians outside of this study, may be administered during an experimental session. Deep brain stimulator (DBS) adjustment - Participants who have had deep brain stimulation implantation as part of their standard-of-care clinical treatment may participate in this study. The patient's stimulator may be adjusted within normal clinical limits during an experimental session.

    Other: Prescribed Medications · Other: Deep brain stimulation adjustment

Interventions

  • OtherPrescribed Medications

    participant's movement disorders medications, prescribed by their treating physician

  • OtherDeep brain stimulation adjustment

    Deep brain stimulator parameters may be adjusted within normal clinical limits

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What researchers measure

Primary outcomes

  1. Neural signal biomarkers

    Spatiotemporal patterns of brain neural activity (neural signal biomarkers / neurophysiologic signatures) associated with movement disorders symptoms.

    Time frame: 5 years

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Study locations

1 of 1 sites recruiting
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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Dec 2025 (actual). Primary completion is estimated for Apr 2030, 52 months after the start.

Of 83 non-industry interventional studies with no phase under Movement Disorders, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 80. This study's planned 52 months is above that.

Counting every sponsor, half of 85 studies reached it within 33 months; a quarter within 11 and three quarters within 80.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 21, 2025
First posted
Feb 27, 2025
StartActual
Dec 10, 2025
Primary completionEst.
Apr 2030
CompletionEst.
Apr 2030
Last update
Jul 14, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06848530
Responsible party
Lauren Hammer (Assistant Professor of Neurology, University of Pennsylvania) — Principal investigator
First posted
Feb 27, 2025
Start date
Dec 10, 2025
Primary completion
Apr 2030 (estimated)
Completion
Apr 2030 (estimated)
Last update
Jul 14, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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