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RecruitingNCT04715984Updated Jun 12, 2026

Corticostriatal Contributions to Parkinson's Disease Cognitive Impairment

An interventional study of Neurophysiology recordings and Neural stimulation in Parkinson Disease, sponsored by Vanderbilt University Medical Center. Recruiting at 1 site in United States. Open to participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2026-06-12.

Sponsored by Vanderbilt University Medical Center · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Started Jun 2021; still recruiting 5 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Not applicable
Ages
40 Years and older
Sex
All
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Study summary

The goal of this study is to learn more about the brain activity underlying Parkinson's disease cognitive impairment. The investigators will utilize neural recordings from corticostriatal structures performed during deep brain stimulation surgery to measure neural activity underlying nonmotor symptoms of Parkinson's disease.

02

Conditions studied

  • Parkinson Disease

Browse trials for

Keywords

  • Deep Brain Stimulation
03

In context

Parkinson Disease

4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.

This study's planned enrollment of 75 is above the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Vanderbilt University Medical Center is the lead sponsor of 824 studies on the registry; 164 are open to participants now.

Of its 122 completed or terminated interventional studies of FDA-regulated products, 91 (75%) have results posted.

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

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Who can participate

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

Inclusion criteria

  • Scheduled to undergo deep brain stimulation surgery under local anesthesia at Vanderbilt University Medical Center
  • Planned clinical electrode trajectory that contacts caudate
  • Age greater than or equal to 40
  • Diagnosis of Parkinson's disease
  • Able to participate in intraoperative testing
  • English speaking

Exclusion criteria

Exclusion criteria:

  • Age less than 40
  • Not able to participate in intraoperative testing (for example unable to comprehend instructions or follow directions)
  • Movement disorder other than Parkinson's disease
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Neural recordings and stimulation

    Other: Neurophysiology recordings · Other: Neural stimulation

Interventions

  • OtherNeurophysiology recordings

    Neurophysiology recordings will be performed during deep brain stimulation surgery and their relationship to performance on a gambling task evaluated

  • OtherNeural stimulation

    Neural stimulation will be delivered during a gambling task and its impact on task performance quantified

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What researchers measure

Primary outcomes

  1. Changes in caudate DLPFC beta coherence

    Caudate DLPFC coherence will be computed at rest and during the gambling task and correlated with cognitive metrics

    Time frame: Baseline to end of Deep Brain Stimulation (DBS), approximately 3-4 hours

  2. Changes in gambling task performance with neural stimulation

    The gambling task will involve seeing a series of cards presented on the screen and pressing a button to respond with a bet. Gambling task performance will be compared between stimulated and non stimulated blocks and between stimulation targets

    Time frame: Baseline to end of Deep Brain Stimulation (DBS), approximately 3-4 hours

Secondary outcomes

  1. Change in beta power with neural stimulation

    Beta power will be computed and compared between stimulation on and off conditions for different targets

    Time frame: Baseline to end of deep brain stimulation (DBS) surgery, approximately 3-4 hours

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Study locations

1 of 1 sites recruiting
  • Vanderbilt University Medical Center
    Nashville, Tennessee 37212, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 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
NCT04715984
Lead sponsor
Vanderbilt University Medical Center
Responsible party
Sarah Bick (Assistant Professor of Neurosurgery, Principal Investigator, Vanderbilt University Medical Center) — Principal investigator
First posted
Jan 20, 2021
Start date
Jun 2, 2021
Primary completion
Aug 2029 (estimated)
Completion
Aug 2029 (estimated)
Last update
Jun 12, 2026

Study contacts

Lucas Chang, BA
Contact
lucas.m.chang@vumc.org
615-421-3046
Sarah Bick, MD
Contact
Sarah.Bick@vumc.org
615-343-9822
Sarah Bick, MD
principal investigator · Vanderbilt University Medical Center

Oversight

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

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