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The Effects of Differing Cognitive Task Demands on Whole-body Energy Metabolism and Cerebral Blood-flow: Modulation by Multivitamins/Minerals and Coenzyme Q10

NCT02381964, Not applicable, Completed, Northumbria University

Trial 10

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

FieldValueSource
TitleThe Effects of Differing Cognitive Task Demands on Whole-body Energy Metabolism and Cerebral Blood-flow: Modulation by Multivitamins/Minerals and Coenzyme Q10ClinicalTrials.gov
NCT numberNCT02381964ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment106 participants, actualClinicalTrials.gov
Lead sponsorNorthumbria UniversityClinicalTrials.gov
ConditionsMetabolic ProcessesClinicalTrials.gov
InterventionsSupradyn® (1RDA+CoQ10), Supradyn® (3RDA), PlaceboClinicalTrials.gov
First posted2015-03-06ClinicalTrials.gov
Last updated2018-03-30ClinicalTrials.gov

Registered outcomes 44

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

ListOutcomeTime frameDescriptionSource
PrimaryConcentration change in oxygenated hemoglobin (Near Infrared Spectroscopy)1 hour post doseClinicalTrials.gov
PrimaryFat oxidation (Indirect calorimetry)1 hour post doseClinicalTrials.gov
PrimaryConcentration change in deoxygenated hemoglobin (Near Infrared Spectroscopy)1 hour post doseClinicalTrials.gov
PrimaryConcentration change in total hemoglobin (Near Infrared Spectroscopy)1 hour post doseClinicalTrials.gov
PrimaryConcentration change in oxygenated hemoglobin (Near Infrared Spectroscopy)56 days post doseClinicalTrials.gov
PrimaryConcentration change in deoxygenated hemoglobin (Near Infrared Spectroscopy)56 days post doseClinicalTrials.gov
PrimaryConcentration change in total hemoglobin (Near Infrared Spectroscopy)56 days post doseClinicalTrials.gov
PrimaryCarbohydrate oxidation (Indirect calorimetry)1 hour post doseClinicalTrials.gov
PrimaryTotal energy expenditure (Indirect calorimetry)1 hour post doseClinicalTrials.gov
PrimaryFat oxidation (Indirect calorimetry)56 days post doseClinicalTrials.gov
PrimaryCarbohydrate oxidation (Indirect calorimetry)56 days post doseClinicalTrials.gov
PrimaryTotal energy expenditure (Indirect calorimetry)56 days post doseClinicalTrials.gov
SecondarySerial 3 subtractions accuracy (Computerised cognitive task)1 hour post doseClinicalTrials.gov
SecondarySerial 3 subtractions accuracy (Computerised cognitive task)56 days post doseClinicalTrials.gov
SecondarySerial 7 subtractions accuracy (Computerised cognitive task)1 hour post doseClinicalTrials.gov
SecondarySerial 7 subtractions accuracy (Computerised cognitive task)56 days post doseClinicalTrials.gov
SecondarySerial 17 subtractions accuracy (Computerised cognitive task)1 hour post doseClinicalTrials.gov
SecondarySerial 17 subtractions accuracy (Computerised cognitive task)56 days post doseClinicalTrials.gov
Secondary3-back task accuracy (Computerised cognitive task)1 hour post doseClinicalTrials.gov
Secondary3-back task reaction time (Computerised cognitive task)1 hour post doseClinicalTrials.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 1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
26870152DERIVEDPubMed

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 1

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

TestNamed asSource
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)