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The Effect of Calcifediol (Hy.D 25 SD/S) and Vitamin D3 on Muscle Strength in a Frail Elderly Population

NCT02349282, Not applicable, Completed, Wageningen University

Trial 10

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

FieldValueSource
TitleThe Effect of Calcifediol (Hy.D 25 SD/S) and Vitamin D3 on Muscle Strength in a Frail Elderly PopulationClinicalTrials.gov
NCT numberNCT02349282ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment78 participants, actualClinicalTrials.gov
Lead sponsorWageningen UniversityClinicalTrials.gov
ConditionsDeficiency, Vitamin D, Elderly, FrailClinicalTrials.gov
InterventionsCalcifediol 10ug/day, Vitamin D3 20ug/day, PlaceboClinicalTrials.gov
First posted2015-01-28ClinicalTrials.gov
Last updated2016-01-11ClinicalTrials.gov

Registered outcomes 16

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

ListOutcomeTime frameDescriptionSource
PrimaryChange in muscle strength, knee extension strength (measured by Biodex System)baseline, week 12, end of study (after 24 weeks supplementation)measured by Biodex SystemClinicalTrials.gov
SecondaryChange in knee flexion strength (measured by Biodex System)baseline, week 12, end of study (after 24 weeks supplementation)measured by Biodex SystemClinicalTrials.gov
SecondaryChange in handgrip strengthbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in SPPBbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in Timed Up and Go testbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in Postural Body Swaybaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in serum Vitamin D3baseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in serum 25(OH)Dbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in serum 1,25(OH)2D3baseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in serum 24,25(OH)2Dbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryFrequency of fallingbaseline, week 12, end of study (after 24 weeks supplementation)ClinicalTrials.gov
SecondaryChange in muscle fibre type and size (Biopsy)baseline, end of study (after 24 weeks supplementation)BiopsyClinicalTrials.gov
SecondaryChange in body composition (DEXA-scan)baseline, end of study (after 24 weeks supplementation)DEXA-scanClinicalTrials.gov
SecondaryChange in cognitive functioning (Trail making, Stroop-test, Letter fluency)baseline, end of study (after 24 weeks supplementation)Trail making, Stroop-test, Letter fluencyClinicalTrials.gov
SecondaryChange in vital Signs (blood pressure and heart rate)baseline, week 12, end of study (after 24 weeks supplementation)blood pressure and heart rateClinicalTrials.gov
SecondaryChange in neuromuscular measurements (MUNIX, MUSIX by EMG)baseline, end of study (after 24 weeks supplementation)MUNIX, MUSIX by EMGClinicalTrials.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 2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
30053278DERIVEDPubMed
31138136DERIVEDPubMed

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
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition
Verbal FluencySecondary 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)