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Effects of Time of Day and Nut Intake on Cognitive Performance

NCT06343142, Not applicable, Completed, Monash University

Trial 10

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

FieldValueSource
TitleEffects of Time of Day and Nut Intake on Cognitive PerformanceClinicalTrials.gov
NCT numberNCT06343142ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment22 participants, actualClinicalTrials.gov
Lead sponsorMonash UniversityClinicalTrials.gov
ConditionsCognitive PerformanceClinicalTrials.gov
InterventionsNuts, Nut-free mealClinicalTrials.gov
First posted2024-04-02ClinicalTrials.gov
Last updated2024-11-22ClinicalTrials.gov

Registered outcomes 15

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

ListOutcomeTime frameDescriptionSource
PrimaryN-back task - accuracybefore meal x 90 min post-mealDifference in the total accuracyClinicalTrials.gov
PrimaryN-back task - matched responsesbefore meal x 90 min post-mealDifference in the % matched responsesClinicalTrials.gov
PrimaryN-back task - false alarmbefore meal x 90 min post-mealDifference in the % false alarmClinicalTrials.gov
PrimaryN-back task - reaction timebefore meal x 90 min post-mealDifference in the reaction time for correct matched responsesClinicalTrials.gov
PrimaryStroop test - congruentbefore meal x 90 min post-mealDifference in the reaction time for congruentClinicalTrials.gov
PrimaryStroop test - incongruentbefore meal x 90 min post-mealDifference in the reaction time for incongruentClinicalTrials.gov
PrimaryStroop test - interferencebefore meal x 90 min post-mealDifference in stroop interference (incongruent - congruent response time)ClinicalTrials.gov
SecondaryMultitasking - pure blocksbefore meal x 90 min post-mealDifference in the reaction time for pure blocksClinicalTrials.gov
SecondaryMultitasking - mixed blocksbefore meal x 90 min post-mealDifference in the reaction time for mixed blocksClinicalTrials.gov
SecondaryMultitasking - mixing costbefore meal x 90 min post-mealDifference in mixing cost (mixed - pure reaction time)ClinicalTrials.gov
SecondarySatiety - hungerHunger will be assessed with a visual analog scale before the meal and 4 times after the meal (15, 30, 60 and 90 mins).Difference in postprandial hungerClinicalTrials.gov
SecondarySatiety - fullnessFullness will be assessed with a visual analog scale before the meal and 4 times after the meal (15, 30, 60 and 90 mins).Difference in postprandial fullnessClinicalTrials.gov
SecondarySatiety - satisfactionSatisfaction will be assessed with a visual analog scale before the meal and 4 times after the meal (15, 30, 60 and 90 mins).Difference in postprandial satisfactionClinicalTrials.gov
SecondarySatiety - eating capacityEating capacity will be assessed with a visual analog scale before the meal and 4 times after the meal (15, 30, 60 and 90 mins).Difference in postprandial eating capacity,ClinicalTrials.gov
SecondarySatiety indexSatiety index will be assessed before the meal and 4 times after the meal (15, 30, 60 and 90 mins).
Difference in postprandial satiety index, calculated using the mean of the four satiety questions, where "hunger" and "eating capacity" will be scored in an inverse way than "fullness" and "satisfaction".
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 3

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

TestNamed asSource
1-Back TaskPrimary outcomeConductCognition
2-Back TaskPrimary outcomeConductCognition
Stroop Color-Word 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)