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Effects of Resistance and Dual-Task Training on Physical, Oculomotor, and Executive Functions in Older Adults With MCI

NCT07278141, Not applicable, Not yet recruiting, Universidad Santo Tomas, Chile

Trial 10

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

FieldValueSource
TitleEffects of Resistance and Dual-Task Training on Physical, Oculomotor, and Executive Functions in Older Adults With MCIClinicalTrials.gov
NCT numberNCT07278141ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment66 participants, estimatedClinicalTrials.gov
Lead sponsorUniversidad Santo Tomas, ChileClinicalTrials.gov
ConditionsPhysical Function, Executive Function (Cognition), Saccadic Eye MovementsClinicalTrials.gov
InterventionsAnaerobic therapeutic exercises (resistance exercise), Anaerobic therapeutic exercises (resistance exercise) plus Dual TaskClinicalTrials.gov
First posted2025-12-11ClinicalTrials.gov
Last updated2025-12-11ClinicalTrials.gov

Registered outcomes 12

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

ListOutcomeTime frameDescriptionSource
PrimaryPhysical-functional condition - Risk of fallsBaseline, and immediately post-intervention (week 11),
The physical-functional condition, specifically the risk of falls of participants will be assessed using the Timed Up and Go Test (TUG). Description: Time in seconds required to stand up from a chair, walk three meters, turn, return, and sit down. Unit of Measure: Seconds (s)
ClinicalTrials.gov
PrimaryExecutive function - Inhibitory controlBaseline, and immediately post-intervention (week 11-12)Participants' inhibitory control will be assessed using the Stroop Colour Test. Performance will be evaluated through response time. Unit of Measure: Milliseconds (ms)ClinicalTrials.gov
PrimaryOculomotor Function- Saccadic and anti-saccadic oculomotor movementBaseline, and immediately post-intervention (week 11)
Saccadic and anti-saccadic eye movements will be assessed using a non-invasive electrooculography (EOG) system (ADInstruments PTK15 EOG model and AD Instruments Brazil PowerLab T26-3079). Two surface electrodes will be placed at the outer canthi of the right and left eyes, with a ground electrode positioned on the forehead. Synchronization between target illumination and EOG signals will be controlled using LabChart software (version 7, Research Ltd.). Performance will be evaluated based on movement latency during visual tasks: left-to-right for saccadic movements and right-to-left for anti-saccadic movements. Unit of Measure: Milliseconds (ms).
ClinicalTrials.gov
PrimaryPhysical - functional condition - Physical functionBaseline, and immediately post-intervention (week 11)
The Physical-functional condition, specifically Participants' physical function will be assessed with the Short Physical Performance Battery (SPPB). Description: Composite score evaluating balance, gait speed, and lower limb strength. Unit of Measure: Points on a scale (0-12).
ClinicalTrials.gov
PrimaryPhysical - functional condition - Grip StrengthBaseline, and immediately post-intervention (week 11)
The Physical-functional condition, specifically the grip strenght of particiants will be assesment with the JAMAR dynamometer. Description: Maximum grip strength measured with a hydraulic dynamometer. Unit of Measure: Kilograms (kg)
ClinicalTrials.gov
PrimaryExecutive Function - Working MemoryBaseline, and immediately post-intervention (week 11-12)
Working memory will be assessed using the Corsi Block-Tapping Test (CBTT), administered in both forward and backward conditions. Performance will be evaluated based on response time for each condition. Unit of Measure: Milliseconds (ms)
ClinicalTrials.gov
PrimaryExecutive Function - Cognitive FlexibilityBaseline, and immediately post-intervention (week 11-12)
Cognitive flexibility will be assessed using the Trail Making Test (TMT). Performance will be evaluated through completion time for Part A (numbers only) and Part B (numbers and letters alternating). Unit of Measure: Miliseconds (ms).
ClinicalTrials.gov
SecondarySociodemographic variable - AgeBaselineAge of participants recorded during the first meeting. Unit of Measure: YearsClinicalTrials.gov
SecondarySociodemographic variable - SexBaselineSex of participants recorded during the first meeting. Unit of Measure: Male/Female (categorical variable).ClinicalTrials.gov
SecondarySociodemographic variables-Educational LevelBaselineHighest educational level attained by participants. Unit of Measure: Categorical variable (e.g., primary, secondary, higher education).ClinicalTrials.gov
SecondaryHealth indicators- ComorbiditiesBaselinePresence of comorbidities such as hypertension, diabetes, or hypercholesterolemia, collected through validated questionnaires. Unit of Measure: Presence/absence (binary categorical variable).ClinicalTrials.gov
SecondaryAnthropometric variable- Body Mass Index (BMI)BaselineBMI calculated according to WHO protocols as weight (kg) divided by height squared (m²). Unit of Measure: kg/m²ClinicalTrials.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 4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
21937887BACKGROUNDPubMed
27567829BACKGROUNDPubMed
30148381BACKGROUNDPubMed
33028159BACKGROUNDPubMed

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
Corsi Block-Tapping TestPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Trail Making Test APrimary outcomeConductCognition
Trail Making Test BPrimary 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)