NCT06848530

Brief 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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
47mo left

Started Dec 2025

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress9%
Dec 2025Apr 2030

First Submitted

Initial submission to the registry

February 21, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 27, 2025

Completed
10 months until next milestone

Study Start

First participant enrolled

December 10, 2025

Completed
4.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2030

Last Updated

March 11, 2026

Status Verified

March 1, 2026

Enrollment Period

4.3 years

First QC Date

February 21, 2025

Last Update Submit

March 8, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Neural signal biomarkers

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

    5 years

Study Arms (2)

Participants without Deep Brain Stimulators

EXPERIMENTAL

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

Participants with Deep Brain Stimulators

EXPERIMENTAL

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 MedicationsOther: Deep brain stimulation adjustment

Interventions

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

Participants with Deep Brain StimulatorsParticipants without Deep Brain Stimulators

Deep brain stimulator parameters may be adjusted within normal clinical limits

Participants with Deep Brain Stimulators

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • \- Patients with dementia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pennsylvania Hospital

Philadelphia, Pennsylvania, 19107, United States

RECRUITING

MeSH Terms

Conditions

Movement Disorders

Condition Hierarchy (Ancestors)

Central Nervous System DiseasesNervous System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Neurology

Study Record Dates

First Submitted

February 21, 2025

First Posted

February 27, 2025

Study Start

December 10, 2025

Primary Completion (Estimated)

April 1, 2030

Study Completion (Estimated)

April 1, 2030

Last Updated

March 11, 2026

Record last verified: 2026-03

Locations