ConductScience.org, home

Library / Trials

Vestibular Balance-Cognition Dual-Task Digital System: Development of a Smart Rehabilitation Platform for the Elderly and Prediction of Balance Function Risks

NCT07735078, Recruiting, National Yang Ming Chiao Tung University

Trial 9

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

FieldValueSource
TitleVestibular Balance-Cognition Dual-Task Digital System: Development of a Smart Rehabilitation Platform for the Elderly and Prediction of Balance Function RisksClinicalTrials.gov
NCT numberNCT07735078ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
Enrollment55 participants, estimatedClinicalTrials.gov
Lead sponsorNational Yang Ming Chiao Tung UniversityClinicalTrials.gov
ConditionsVestibular Dysfunction, Dizziness, Falls (Accidents) in Old Age, Balance Assessment, Cognitive Function Decline, Dual-Task PerformanceClinicalTrials.gov
InterventionsInstrumented balance and gait assessment using wearable inertial sensors, Questionnaires and paper-based cognitive testsClinicalTrials.gov
First posted2026-07-29ClinicalTrials.gov
Last updated2026-07-29ClinicalTrials.gov

Registered outcomes 22

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

ListOutcomeTime frameDescriptionSource
PrimaryGait speedBaseline laboratory assessment (single visit in year 1)Average forward velocity of whole-body progression during walking, calculated as total distance divided by time.ClinicalTrials.gov
PrimaryStride length (m)Baseline laboratory assessment (single visit in year 1)Linear distance between two consecutive initial contacts of the same foot.ClinicalTrials.gov
PrimaryStep width (m)Baseline laboratory assessment (single visit in year 1)Mediolateral distance between consecutive foot placements, representing base of support during gait.ClinicalTrials.gov
PrimaryCadence (steps/min)Baseline laboratory assessment (single visit in year 1)Number of steps taken per minute during walking.ClinicalTrials.gov
PrimaryStep-to-step variability (%)Baseline laboratory assessment (single visit in year 1)Variability of consecutive steps, typically quantified as the coefficient of variation of stride time or step length.ClinicalTrials.gov
PrimaryTrunk angular velocity (degrees/s)Baseline laboratory assessment (single visit in year 1)Rate of change in trunk segment orientation over time, derived from rotational kinematics.ClinicalTrials.gov
PrimaryTrunk angular displacement (degrees)Baseline laboratory assessment (single visit in year 1)Magnitude of trunk segment rotation relative to a reference orientation.ClinicalTrials.gov
PrimaryCenter-of-mass displacement (m)Baseline laboratory assessment (single visit in year 1)Spatial excursion of the body's center of mass, typically analyzed in anterior-posterior and mediolateral directions during standing.ClinicalTrials.gov
PrimaryResponse time (s or ms)Baseline laboratory assessment (single visit in year 1)Time elapsed between stimulus onset and initiation of a motor response.ClinicalTrials.gov
SecondaryMontreal Cognitive Assessment-Taiwan version score (0-30points)Baseline laboratory assessmentTotal score on the Montreal Cognitive Assessment-Taiwan version, representing global cognitive function.ClinicalTrials.gov
SecondaryPath tracing completion time (s)Baseline laboratory assessmentTime required to complete the Color Trails Test-1 task.ClinicalTrials.gov
SecondaryStroop test score (count as PR1-99%)Baseline laboratory assessmentScore of Stroop-type task, indicating inhibitory control and selective attention.ClinicalTrials.gov
SecondaryWorking memory completion time (s)Baseline laboratory assessmentTime required to complete the Color Trails Test-2 task.ClinicalTrials.gov
SecondaryMental rotation accuracy (number of correct responses)(0-16)Baseline laboratory assessmentNumber of correct responses in the mental rotation task, reflecting visuospatial processing ability.ClinicalTrials.gov
SecondaryMental rotation completion time (s)Baseline laboratory assessmentTime required to complete the mental rotation task.ClinicalTrials.gov
SecondaryActivities-specific Balance Confidence score (0-100 points)Baseline laboratory assessmentTotal score on the Activities-specific Balance Confidence (ABC) scale, reflecting perceived balance confidence during daily activities; higher scores indicate greater confidence.ClinicalTrials.gov
SecondaryDizziness Handicap Inventory score (0-100points)Baseline laboratory assessmentTotal score on the Dizziness Handicap Inventory (DHI), representing self-perceived handicap due to dizziness; higher scores indicate greater disability.ClinicalTrials.gov
SecondaryHospital Anxiety and Depression Scale - Anxiety score (0-21 points)Baseline laboratory assessmentSubscale score of the HADS assessing anxiety symptoms; higher scores indicate greater anxiety.ClinicalTrials.gov
SecondaryHospital Anxiety and Depression Scale - Depression score (0-21 points)Baseline laboratory assessmentSubscale score of the HADS assessing depressive symptoms; higher scores indicate greater depression.ClinicalTrials.gov
SecondaryVisual Vertigo Analogue Scale score ( 0-90points)Baseline laboratory assessmentSelf-reported severity of visually induced dizziness measured using a visual analogue scale; higher scores indicate greater symptom severity.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 2

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

TestNamed asSource
Mental RotationSecondary outcomeConductCognition
Stroop Color-Word TestSecondary 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)