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Neuroplasticity in Parkinson's Disease

NCT05286736, Completed, University of Minnesota

Trial 9

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleNeuroplasticity in Parkinson's DiseaseClinicalTrials.gov
NCT numberNCT05286736ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
Enrollment42 participants, actualClinicalTrials.gov
Lead sponsorUniversity of MinnesotaClinicalTrials.gov
ConditionsParkinson, Parkinson DiseaseClinicalTrials.gov
InterventionsNeuroimaging, Quantitative assessmentsClinicalTrials.gov
First posted2022-03-18ClinicalTrials.gov
Last updated2026-11-03ClinicalTrials.gov

Registered outcomes 10

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in volume of Subthalamic NucleusBaseline, 30-36 monthsThe volume of the subthalamic nucleus is assessed using MRI and reported in millimeters cubed (mm\^3).ClinicalTrials.gov
PrimaryChange in fractional Anisotropy of Subthalamic NucleusBaseline, 30-36 months
Fractional anisotropy, measured using MRI, is a unit-less value between zero and one that describes the degree of anisotropy of water diffusion in a specified brain area. Higher values indicate a greater degree of anisotropy, while a score of zero indicates isotropic diffusion.
ClinicalTrials.gov
PrimaryChange in cortico-STN ConnectivityBaseline, 30-36 monthsCortico-Subthalamic nucleus connectivity is measured using MRI and reported as a z score (unitless).ClinicalTrials.gov
PrimaryChange in paired Associative Stimulation-Motor Evoked Potential (PAS-MEP)Baseline, 30-36 monthsMotor evoked potential is measured as the amplitude of change in target muscle electrical activity following transcranial magnetic stimulation (TMS) and reported in units of millivolts (mV).ClinicalTrials.gov
PrimaryChange in Mattis Dementia Rating Scale 2 (DRS-2)Baseline, 30-36 months
The DRS-2 consists of 24 items, rated on a scale from 0 to 6. Item scores are combined into five subscales: attention (8 items), initiation/perseveration (11 items), construction (6 items), conceptualization ( 6 items), and memory (5 items). These five subscale scores are summed to calculate a total score ranging from from 0 to 144 points, with lower scores indicating worse performance due to dementia.
ClinicalTrials.gov
PrimaryChange in Rey Complex Figure and Matrix Reasoning of the Wechsler Adult Intelligence Scale - IVBaseline, 30-36 monthsMeasure of visuospatial construction, memory and reasoning. Scaled score based on age norms.ClinicalTrials.gov
PrimaryChange in Stroop Color Word TestBaseline, 30-36 monthsMeasure of response inhibition, selective attention and processing. Scaled score based on age norms.ClinicalTrials.gov
PrimaryChange in Wisconsin Card Sorting TestBaseline, 30-36 monthsMeasures cognitive flexibility, abstract reasoning, and set-shifting. Scaled score based on age norms.ClinicalTrials.gov
PrimaryChange in Delis-Kaplan Executive Function System (D-KEFS) Verbal Fluency SubtestBaseline, 30-36 monthsMeasures cognitive flexibility, abstract reasoning, and set-shifting. Scaled score based on age norms.ClinicalTrials.gov
PrimaryChange in Brief Visuospatial Memory Test - Revised (BVMT-R)Baseline, 30-36 monthsMeasure of non-verbal (visuospatial) learning and memory abilities. Scaled score based on age norms.ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 5

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Card Sorting Test (Berg)Primary outcomeConductCognition
Complex Figure Copy and RecallPrimary outcomeConductCognition
Matrix ReasoningPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Verbal FluencyPrimary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)