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High-Intensity Exercise in Older Adults

NCT06199661, Not applicable, Completed, University of California, Berkeley

Trial 10

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

FieldValueSource
TitleHigh-Intensity Exercise in Older AdultsClinicalTrials.gov
NCT numberNCT06199661ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment4 participants, actualClinicalTrials.gov
Lead sponsorUniversity of California, BerkeleyClinicalTrials.gov
ConditionsFunctional Fitness, Cognitive AbilitiesClinicalTrials.gov
InterventionsAPEXClinicalTrials.gov
First posted2024-01-10ClinicalTrials.gov
Last updated2024-01-10ClinicalTrials.gov

Registered outcomes 18

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

ListOutcomeTime frameDescriptionSource
PrimaryAttendance Rate4 weeks during interventionThe number of classes attended out of eight total classes.ClinicalTrials.gov
PrimaryHeart Rate4 weeks during interventionHeart rate measured in beats per minute.ClinicalTrials.gov
PrimaryFunctional Reach Test DistanceOnce 3-7 days before start of intervention and once 0-2 days after end of interventionThe distance in inches of an individual's forward reach with one arm while maintaining a standing position with feet flat on the floor at hip width.ClinicalTrials.gov
PrimaryTimed Up-And-Go TimeOnce 3-7 days before start of intervention and once 0-2 days after end of interventionThe number of seconds for an individual to rise from a seated position, walk eight feet, turn around, and return to a seated position.ClinicalTrials.gov
PrimaryNumber of Steps in 2-minute Step TestOnce 3-7 days before start of intervention and once 0-2 days after end of interventionThe number of right knee raises completed in two minutes while marching in place and raising each knee to a point midway between the patella (kneecap) and iliac crest (top hip bone).ClinicalTrials.gov
PrimaryNumber of Repetitions in 30-Second Chair Stand TestOnce 3-7 days before start of intervention and once 0-2 days after end of interventionThe number of sit-to-stands completed in 30 seconds on a standard 17" seat-height chair with arms folded across the chest.ClinicalTrials.gov
PrimaryVisual Search Task AccuracyOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionNumber of correct trialsClinicalTrials.gov
PrimaryVisual Search Task Reaction TimeOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionReaction time on correct trials in secondsClinicalTrials.gov
PrimaryForward Digit SpanOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionThe length of the longest sequence of random digits that a participant can correctly recall twice.ClinicalTrials.gov
PrimaryBackward Digit SpanOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionThe length of the longest sequence of random digits that a participant can correctly report backward twice.ClinicalTrials.gov
PrimaryForward Spatial SpanOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionThe length of the longest sequence of random positions that a participant can correctly recall.ClinicalTrials.gov
PrimaryBackward Spatial SpanOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionThe length of the longest sequence of random positions that a participant can correctly report backward.ClinicalTrials.gov
PrimaryGo/No-Go Task HitsOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionHits are the proportion of correct responses on trials when "go" is presented.ClinicalTrials.gov
PrimaryGo/No-Go Task Reaction TimesOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionReaction times are for hit trials only (correct responses when "go" is presented) in seconds.ClinicalTrials.gov
PrimaryFlanker Task AccuracyOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionNumber of correct trials.ClinicalTrials.gov
PrimaryFlanker Task Reaction TimesOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionReaction time on correct trials in seconds.ClinicalTrials.gov
PrimaryStroop Task AccuracyOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionNumber of correct trials.ClinicalTrials.gov
PrimaryStroop Task Reaction TimesOnce 10-14 days before start of intervention, once 3-7 days before start of intervention, and once 0-2 days after end of interventionReaction time on correct trials in seconds.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 5

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 TestPrimary outcomeConductCognition
Eriksen Flanker TaskPrimary outcomeConductCognition
Go/No-Go TaskPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Visual Search TestPrimary 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)