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Centre- Versus Home-based Exercise for MCI and Early Dementia

NCT02774720, Not applicable, Completed, University of Waterloo

Trial 10

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

FieldValueSource
TitleCentre- Versus Home-based Exercise for MCI and Early DementiaClinicalTrials.gov
NCT numberNCT02774720ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment44 participants, actualClinicalTrials.gov
Lead sponsorUniversity of WaterlooClinicalTrials.gov
ConditionsMild Cognitive Impairment, DementiaClinicalTrials.gov
InterventionsCentre-based exercise, Home-based exerciseClinicalTrials.gov
First posted2016-05-17ClinicalTrials.gov
Last updated2019-05-29ClinicalTrials.gov

Registered outcomes 14

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

ListOutcomeTime frameDescriptionSource
PrimaryAchievement of Physical Activity3 monthsPercent achievement of physical activity recommendations (150min/wk of moderate or high intensity physical activity) as objectively measured using an activity monitor.ClinicalTrials.gov
PrimaryChange in physical activitybaseline to 3 monthsChange in physical activity as objectively measured using an activity monitor.ClinicalTrials.gov
SecondaryCost-effectiveness3 monthsCost of resource utilization per minute change in physical activity.ClinicalTrials.gov
OtherChange in cognitive function as characterized by Alzheimer's Disease Assessment Scale - Cognition (ADAS-Cog)baseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in cognitive function as characterized by the Stroop taskbaseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in cognitive function as characterized by the Trail making taskbaseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in cognitive function as characterized by the semantic fluencybaseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in physical function as characterized by the Short Physical Performance Battery (SPPB) scoresbaseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in quality of life as measured with the EuroQol five dimensions questionnaire (EQ-5D)baseline to 3 monthsChange in continuous scoresClinicalTrials.gov
OtherChange in mood as measured with the Neuropsychiatric Inventory Questionnaire (NPI-Q) (depression/dysphoria, anxiety, apathy/indifference scales)baseline to 3 monthsChange in scores, number meeting screening criteria for depressionClinicalTrials.gov
OtherChange in daily function as characterized using the 6-item Disability Assessment for Dementia (DAD-6)baseline to 3 monthsChange in scoreClinicalTrials.gov
OtherChange in body mass index (BMI)baseline to 3 monthsChange in scoreClinicalTrials.gov
OtherChange in waist circumferencebaseline to 3 monthsChange in scoreClinicalTrials.gov
OtherChange in blood pressurebaseline to 3 monthsChange in number with high blood pressure (\>140 systolic blood pressure (SBP), \>90 diastolic blood pressure (DBP))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 1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
29370756DERIVEDPubMed

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
Category FluencyOther outcomeConductCognition
Stroop Color-Word TestOther outcomeConductCognition
Trail Making Test AOther outcomeConductCognition
Trail Making Test BOther 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)