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Effects of Paraxanthine Supplementation on eSport Performancre

NCT07533045, Not applicable, Completed, Lindenwood University

Trial 10

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

FieldValueSource
TitleEffects of Paraxanthine Supplementation on eSport PerformancreClinicalTrials.gov
NCT numberNCT07533045ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment60 participants, actualClinicalTrials.gov
Lead sponsorLindenwood UniversityClinicalTrials.gov
ConditionsCognitive Function, Gaming PerformanceClinicalTrials.gov
InterventionsPlacebo, ParaxanthineClinicalTrials.gov
First posted2026-04-16ClinicalTrials.gov
Last updated2026-04-16ClinicalTrials.gov

Registered outcomes 9

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

ListOutcomeTime frameDescriptionSource
PrimaryGaming Performance ScoreTime Frame: Change from baseline (Week 0) to Week 6
Electronic gaming performance will be assessed using standardized gameplay metrics collected during 60- and 120-minute gaming sessions. Primary variables include knock-outs, falls, damage given, damage taken, hit percentage, and peak damage.
ClinicalTrials.gov
PrimaryTrail Making Test Part A (Completion Time)Time Frame: Change from baseline (Week 0) to Week 6Cognitive processing speed and visual attention will be assessed using Trail Making Test Part A, including total time to completion.ClinicalTrials.gov
PrimaryTrail Making Test Part B (Completion Time)Time Frame: Change from baseline (Week 0) to Week 6Cognitive processing speed and visual attention will be assessed using Trail Making Test Part B, including total time to completion.ClinicalTrials.gov
PrimaryTrail Making Test Part A (Errors)Time Frame: Change from baseline (Week 0) to Week 6Cognitive processing speed and visual attention will be assessed using Trail Making Test Part A, including total number of errors.ClinicalTrials.gov
PrimaryTrail Making Test Part B (Errors)Time Frame: Change from baseline (Week 0) to Week 6Cognitive processing speed and visual attention will be assessed using Trail Making Test Part B, including total number of errors.ClinicalTrials.gov
PrimaryStroop Color and Word Test PerformanceTime Frame: Change from baseline (Week 0) to Week 6Cognitive performance will be assessed using the Stroop Color and Word Test, including response time and accuracy.ClinicalTrials.gov
PrimaryProfile of Mood States (POMS) Total Mood Disturbance ScoreTime Frame: Change from baseline (Week 0) to Week 6Mood state will be assessed using the Profile of Mood States questionnaire, with calculation of total mood disturbance score.ClinicalTrials.gov
PrimaryPittsburgh Sleep Quality Index (PSQI) ScoreTime Frame: Change from baseline (Week 0) to Week 6Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI) global score.ClinicalTrials.gov
PrimaryHeart Rate Variability (HRV)Time Frame: Change from baseline (Week 0) to Week 6Autonomic function will be assessed using heart rate variability metrics including RMSSD, high-frequency power, low-frequency power, and LF:HF ratio.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
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)