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Stair Climbing Exercise Versus Traditional Resistance Exercise

NCT05263115, Not applicable, Completed, KU Leuven

Trial 10

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

FieldValueSource
TitleStair Climbing Exercise Versus Traditional Resistance ExerciseClinicalTrials.gov
NCT numberNCT05263115ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment46 participants, actualClinicalTrials.gov
Lead sponsorKU LeuvenClinicalTrials.gov
ConditionsExercise TrainingClinicalTrials.gov
InterventionsResistance Exercise intervention, Functional stair climbing and stepping-based exercise interventionClinicalTrials.gov
First posted2022-03-02ClinicalTrials.gov
Last updated2023-01-23ClinicalTrials.gov

Registered outcomes 11

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

ListOutcomeTime frameDescriptionSource
PrimaryF-V profileChange from baseline in F-v profile at 12 weeks
Force-velocity profiling is carried out unilaterally (dominant leg) on the pneumatic leg press device (Leg Press CC, HUR, Kokkola, Finland). The test protocol consists of a maximal isometric test (knee joint angle = 85°, hip angle = 55°; 3 attempts of 3s), followed by explosive concentric leg extensions at gradually increasing loads (unloaded, 15%, 30%, 45%, 60%, 75% of the maximal isometric force, 2-3 attempts per load, and additional single repetitions until one-repetition maximum is reached). Mean velocity of the best trial per load is used to estimate the individual F-v relationship through a linear equation. This F-v relationship will be used to examine the exercise-induced adaptations. F0 (maximal force), v0 (maximal velocity), a (the equation's slope), Pmax (maximal power) and the corresponding v and F at Pmax are used for the analyses.
ClinicalTrials.gov
SecondaryGait speedChange from baseline in gait speed at 12 weeksThe average speed to walk 10m as fast as possible (in m/s)ClinicalTrials.gov
Secondary5-repetition sit-to-stand timeChange from baseline in sit-to-stand performance at 12 weeksThe time (s) needed to perform 5 sit-to-stand transitions.ClinicalTrials.gov
Secondary5-repetition sit-to-stand powerChange from baseline in sit-to-stand performance at 12 weeksThe power (watt) needed to perform 5 sit-to-stand transitions.ClinicalTrials.gov
SecondaryStair ascent timeChange from baseline in stair climbing performance at 12 weeks.The time (s) needed to ascend a flight of stairs.ClinicalTrials.gov
SecondaryStair ascent powerChange from baseline in stair climbing performance at 12 weeks.The power (watt) needed to ascend a flight of stairs.ClinicalTrials.gov
SecondaryCountermovement jump heightChange from baseline in countermovement jump height at 12 weeks.Jump height (cm) in a countermovement jumpClinicalTrials.gov
SecondaryMoCA test scoreChange from baseline in Montrial Cognitive Assessment test score at 12 weeks.Total score (min 0, max 30, higher scores indicate better performance) on the Montreal Cognitive Assessment testClinicalTrials.gov
SecondaryDigit Span Test scoreChange from baseline in Digit Span Test score at 12 weeks.Total score (min 0, max 30, higher scores indicate better performance) on the Digit Span TestClinicalTrials.gov
SecondaryTrail Making Test TimeChange from baseline in Trail Making Test at 12 weeks.Total duration (s) needed to complete the Trail Making Test.ClinicalTrials.gov
SecondaryStroop Test number of wordsChange from baseline in Stroop Test at 12 weeks.Total number of words red in 45s in the stroop test.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
39590559DERIVEDPubMed

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
Digit Span TestSecondary outcomeConductCognition
Stroop Color-Word TestSecondary 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)