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Physical Training for People With Parkinson's Disease and Multiple Sclerosis: Effect on Mind and Body

NCT05357638, Not applicable, Unknown, Amsterdam UMC, location VUmc

Trial 10

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

FieldValueSource
TitlePhysical Training for People With Parkinson's Disease and Multiple Sclerosis: Effect on Mind and BodyClinicalTrials.gov
NCT numberNCT05357638ClinicalTrials.gov
StatusUnknownClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment48 participants, estimatedClinicalTrials.gov
Lead sponsorAmsterdam UMC, location VUmcClinicalTrials.gov
ConditionsParkinson Disease, Multiple SclerosisClinicalTrials.gov
InterventionsHigh Intensity Interval Training (HIIT), Continuous Aerobic Training (CAT), Movement AdviceClinicalTrials.gov
First posted2022-05-03ClinicalTrials.gov
Last updated2023-04-25ClinicalTrials.gov

Registered outcomes 25

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

ListOutcomeTime frameDescriptionSource
PrimaryChange in anxiety and depressive symptomsBaseline (week 0), week 4, week 12, week 16The effect of physical training on anxiety and depressive symptoms, measured by the Hospital Anxiety and Depression ScaleClinicalTrials.gov
SecondaryChange in disease severityBaseline (week 0), week 4, week 12, week 16
The effect of physical training on disease severity, measured by the Unified Parkinson's Disease Rating Scale (Parkinson's disease) (total score range 0-199, higher score = worse) or Expanded Disability Status Scale (Multiple Sclerosis)
ClinicalTrials.gov
SecondaryChange in cognitive function (i.e., ability to inhibit cognitive interference)Baseline (week 0), week 4, week 12, week 16The effect of physical training on cognitive function, measured by the Stroop Color Word TestClinicalTrials.gov
SecondaryChange in cognitive function (i.e., mental flexibility)Baseline (week 0), week 4, week 12, week 16The effect of physical training on cognitive function, measured by the Trail Making TestClinicalTrials.gov
SecondaryChange in cognitive function (i.e., range of cognitive operations: motor speed, attention, and visuoperceptual functions)Baseline (week 0), week 4, week 12, week 16The effect of physical training on cognitive function, measured by the Symbol Digit Modalities TestClinicalTrials.gov
SecondaryChange in fatigueBaseline (week 0), week 4, week 12, week 16The effect of physical training on fatigue, measured by the Checklist Individual Strength fatigue sub-scaleClinicalTrials.gov
SecondaryChange in sleep qualityBaseline (week 0), week 4, week 12, week 16The effect of physical training on sleep quality, measured by the Insomnia Severity IndexClinicalTrials.gov
SecondaryChange in well-beingBaseline (week 0), week 4, week 12, week 16The effect of physical training on well-being, measured by the Parkinson's Disease Questionnaire (8 items) (Parkinson's disease) or Multiple Sclerosis Impact Scale (29 items) (Multiple Sclerosis)ClinicalTrials.gov
SecondaryChange in quality of lifeBaseline (week 0), week 4, week 12, week 16The effect of physical training on quality of life, measured by the Short Form health survey (36 items)ClinicalTrials.gov
SecondaryChange in motor capacity (i.e., walking speed)Baseline (week 0), week 4, week 12, week 16The effect of physical training on motor capacity, measured by the 10-Meter Walk TestClinicalTrials.gov
SecondaryChange in motor capacity (i.e., lower extremity function, mobility, and fall risk)Baseline (week 0), week 4, week 12, week 16The effect of physical training on motor capacity, measured by the Timed Up and Go testClinicalTrials.gov
SecondaryChange in motor capacity (i.e., finger dexterity)Baseline (week 0), week 4, week 12, week 16The effect of physical training on motor capacity, measured by the Nine Hole Peg TestClinicalTrials.gov
SecondaryChange in activities of daily livingBaseline (week 0), week 4, week 12, week 16The effect of physical training on activities of daily living, measured by the Nottingham Extended Activities of daily living IndexClinicalTrials.gov
SecondaryChange in biomarkers of neuroplasticity in bloodBaseline (week 0), week 4, week 12, week 16The effect of physical training on biomarkers of neuroplasticity in blood, measured by Brain Derived Neurotrophic Factor concentrationClinicalTrials.gov
SecondaryChange in biomarkers of neurodegeneration in bloodBaseline (week 0), week 4, week 12, week 16The effect of physical training on biomarkers of neurodegeneration in blood, measured by Neurofilament Light concentrationClinicalTrials.gov
SecondaryChange in brain morphologyWeek 4, week 12The effect of physical training on brain morphology, measured by structural magnetic resonance imaging (MRI)ClinicalTrials.gov
SecondaryChange in structural brain connectivityWeek 4, week 12The effect of physical training on structural brain connectivity, measured by diffusion MRI + free-water contentClinicalTrials.gov
SecondaryChange in brain connectivityWeek 4, week 12The effect of physical training on brain connectivity, measured by resting state functional MRIClinicalTrials.gov
SecondaryChange in brain iron concentration in the Substantia NigraWeek 4, week 12The effect of physical training on brain iron concentration in the Substantia Nigra, measured by Quantitative Susceptibility Mapping methodologyClinicalTrials.gov
SecondaryChange in brain neuromelanin contentWeek 4, week 12The effect of physical training on brain neuromelanin content, measured by neuromelanin-sensitive MRIClinicalTrials.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 4

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

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition
Symbol CodingSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary 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)