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The Effect of Acute Concurrent Exercise on Executive Function: An Event-Related Potential Study

NCT05314634, Not applicable, Completed, National Taiwan Normal University; results first posted 2025-02-20

Trial 11

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

FieldValueSource
TitleThe Effect of Acute Concurrent Exercise on Executive Function: An Event-Related Potential StudyClinicalTrials.gov
NCT numberNCT05314634ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment78 participants, actualClinicalTrials.gov
Lead sponsorNational Taiwan Normal UniversityClinicalTrials.gov
ConditionsExecutive FunctionClinicalTrials.gov
Interventionsconcurrent exercise, aerobic exerciseClinicalTrials.gov
First posted2022-04-06ClinicalTrials.gov
Last updated2025-02-20ClinicalTrials.gov
Results first posted2025-02-20ClinicalTrials.gov

Registered outcomes 3

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

ListOutcomeTime frameDescriptionSource
PrimaryTask Switch Test Response Times30 minutes
The shifting aspect of executive function was assessed using a computerised task-switching test. Each participant (N=78) completed 384 trials across six blocks (64 trials per block). The test consisted of two types of cognitive tasks: (1) number magnitude judgment (greater/less than 5) for digits 1-9 presented in solid-line squares, and (2) odd/even judgment for numbers presented in dotted-line squares. Performance was analysed by calculating each participant's mean response time (milliseconds) under four conditions: Homogeneous condition: Blocks where participants performed the same task repeatedly (Blocks 1 \& 2, e.g., AAAA or BBBB) Heterogeneous condition: Blocks where tasks were mixed (Blocks 3-6, e.g., AABBAA) Non-switch trials: Consecutive trials of the same task type within heterogeneous blocks (e.g., AA or BB) Switch trials: Trials where the task changed from the previous trial within heterogeneous blocks (e.g., AB or BA) Lower response time represents better task perform
ClinicalTrials.gov
OtherBlood Lactatebefore intervention, 17 minutes after intervention, and immediately after the 35 minute intervention
The lactic acid system is one of the important systems of human energy metabolism. In addition to supplying energy to muscles, it can also be used as an energy source for brain energy metabolism. When people doing exercise, the concentration of blood lactate will be increased, and the lactate acid system will replace the glucose system as the main energy source for the brain. In the present study, blood lactate were collected from fingertip with a lancet and measured by lactate analyzer before, 17 minutes after, and after intervention.
ClinicalTrials.gov
OtherStroop Task30 minutes
The Stroop task consists of neutral, congruent, and incongruent trials. In neutral trials, colored rectangles were presented and participants were instructed to respond to whether the squares were red, blue, or green. For congruent and incongruent trials, participants were presented with the names of the three Chinese color words of 紅 (red), 藍 (blue), or 綠 (green) printed in either the same (congruent) or different (incongruent) ink color and instructed to respond to the color of the ink while inhibiting the meaning of the word.
ClinicalTrials.gov

Outcomes 3

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource
PRIMARYTask Switch Test Response Times30 minutes
The analysis was based on participants' mean response times under four cognitive conditions (Homogeneous, Heterogeneous, Non-switch, and Switch), derived from their performance across 384 trials (6 blocks × 64 trials).
millisecondMEANClinicalTrials.gov
OTHER_PRE_SPECIFIEDBlood Lactatebefore intervention, 17 minutes after intervention, and immediately after the 35 minute intervention
Blood lactate samples were collected from fingertip with a lancet and measured by lactate analyzer at three time points: before, 17 minutes after, and after intervention (three blood samples were collected from each participant).
mmol/lMEANClinicalTrials.gov
OTHER_PRE_SPECIFIEDStroop Task30 minutesGiven temporal constraints, the Stroop task was not measured in this study.ClinicalTrials.gov

Results by group 21

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource
Task Switch Test Response TimesConcurrent Exercise Group, CEHeterogeneous783.97Standard Error 11.65millisecondClinicalTrials.gov
Task Switch Test Response TimesAerobic Exercise Group, AEHeterogeneous788.76Standard Error 11.66millisecondClinicalTrials.gov
Task Switch Test Response TimesReading Control Group, RCHeterogeneous839.46Standard Error 11.65millisecondClinicalTrials.gov
Task Switch Test Response TimesConcurrent Exercise Group, CEHomogeneous566.46Standard Error 14.67millisecondClinicalTrials.gov
Task Switch Test Response TimesAerobic Exercise Group, AEHomogeneous547.82Standard Error 14.70millisecondClinicalTrials.gov
Task Switch Test Response TimesReading Control Group, RCHomogeneous618.30Standard Error 14.72millisecondClinicalTrials.gov
Task Switch Test Response TimesConcurrent Exercise Group, CENon-switch737.73Standard Error 11.63millisecondClinicalTrials.gov
Task Switch Test Response TimesAerobic Exercise Group, AENon-switch753.98Standard Error 11.62millisecondClinicalTrials.gov
Task Switch Test Response TimesReading Control Group, RCNon-switch797.48Standard Error 11.62millisecondClinicalTrials.gov
Task Switch Test Response TimesConcurrent Exercise Group, CESwitch833.32Standard Error 13.34millisecondClinicalTrials.gov
Task Switch Test Response TimesAerobic Exercise Group, AESwitch825.39Standard Error 13.34millisecondClinicalTrials.gov
Task Switch Test Response TimesReading Control Group, RCSwitch882.18Standard Error 13.34millisecondClinicalTrials.gov
Blood LactateConcurrent Exercise Group, CEBefore intervention2.95Standard Error 0.32mmol/lClinicalTrials.gov
Blood LactateAerobic Exercise Group, AEBefore intervention3.09Standard Error 0.32mmol/lClinicalTrials.gov
Blood LactateReading Control Group, RCBefore intervention2.4Standard Error 0.32mmol/lClinicalTrials.gov
Blood LactateConcurrent Exercise Group, CESeventeen minutes after intervention5.58Standard Error 0.41mmol/lClinicalTrials.gov
Blood LactateAerobic Exercise Group, AESeventeen minutes after intervention5.27Standard Error 0.41mmol/lClinicalTrials.gov
Blood LactateReading Control Group, RCSeventeen minutes after intervention2.13Standard Error 0.41mmol/lClinicalTrials.gov
Blood LactateConcurrent Exercise Group, CEAfter intervention8.94Standard Error 0.44mmol/lClinicalTrials.gov
Blood LactateAerobic Exercise Group, AEAfter intervention4.65Standard Error 0.44mmol/lClinicalTrials.gov

Participant flow 9

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource
Overall StudySTARTEDConcurrent Exercise Group, CE26ClinicalTrials.gov
Overall StudySTARTEDAerobic Exercise Group, AE26ClinicalTrials.gov
Overall StudySTARTEDReading Control Group, RC26ClinicalTrials.gov
Overall StudyCOMPLETEDConcurrent Exercise Group, CE26ClinicalTrials.gov
Overall StudyCOMPLETEDAerobic Exercise Group, AE26ClinicalTrials.gov
Overall StudyCOMPLETEDReading Control Group, RC26ClinicalTrials.gov
Overall StudyNOT COMPLETEDConcurrent Exercise Group, CE0ClinicalTrials.gov
Overall StudyNOT COMPLETEDAerobic Exercise Group, AE0ClinicalTrials.gov
Overall StudyNOT COMPLETEDReading Control Group, RC0ClinicalTrials.gov

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 9

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource
Total, all-cause mortalityConcurrent Exercise Group, CE026ClinicalTrials.gov
Total, all-cause mortalityAerobic Exercise Group, AE026ClinicalTrials.gov
Total, all-cause mortalityReading Control Group, RC026ClinicalTrials.gov
Total, other adverse eventsConcurrent Exercise Group, CE026ClinicalTrials.gov
Total, other adverse eventsAerobic Exercise Group, AE026ClinicalTrials.gov
Total, other adverse eventsReading Control Group, RC026ClinicalTrials.gov
Total, serious adverse eventsConcurrent Exercise Group, CE026ClinicalTrials.gov
Total, serious adverse eventsAerobic Exercise Group, AE026ClinicalTrials.gov
Total, serious adverse eventsReading Control Group, RC026ClinicalTrials.gov

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
Task Switching TestPrimary outcomeConductCognition
Stroop Color-Word TestOther 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)