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A Trial of Cognitive Training in Euthymic Bipolar Disorder

NCT02476331, Not applicable, Withdrawn, University of Calgary

Trial 10

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

FieldValueSource
TitleA Trial of Cognitive Training in Euthymic Bipolar DisorderClinicalTrials.gov
NCT numberNCT02476331ClinicalTrials.gov
StatusWithdrawnClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment0 participants, actualClinicalTrials.gov
Lead sponsorUniversity of CalgaryClinicalTrials.gov
ConditionsBipolar DisorderClinicalTrials.gov
InterventionsWorking memory trainingClinicalTrials.gov
First posted2015-06-19ClinicalTrials.gov
Last updated2016-05-17ClinicalTrials.gov

Registered outcomes 11

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

ListOutcomeTime frameDescriptionSource
PrimaryWorking memory capacityChange from baseline to post-assessment (after 10 weeks of training)Measured with the Automated Operation Span task (AOSPAN), Wechsler Adult Intelligence Scale (WAIS-IV) Digit Span and Maintenance and Manipulation taskClinicalTrials.gov
PrimaryEmotion regulationChange from baseline to post-assessment (after 10 weeks of training)Measured with the Emotional Stroop task and Emotional N-back taskClinicalTrials.gov
PrimaryFluid intelligenceChange from baseline to post-assessment (after 10 weeks of training)Measured with the Raven's Progressive Matrices (RPM) taskClinicalTrials.gov
SecondaryDepression symptom severityChange from baseline to post-assessment (after 10 weeks of training)Measured with the 17-item Hamilton Rating Scale for Depression (HRDS-17)ClinicalTrials.gov
SecondaryManic symptom severityChange from baseline to post-assessment (after 10 weeks of training)Measured with the Young Mania Rating Scale (YMRS)ClinicalTrials.gov
SecondaryCommunity functioningChange from baseline to post-assessment (after 10 weeks of training)Measured with the Functioning Assessment Short Test (FAST)ClinicalTrials.gov
OtherDecision making and impulsivityChange from baseline to post-assessment (after 10 weeks of training)Measured with the Delay Discounting TaskClinicalTrials.gov
OtherExecutive functioning: inhibition and set shiftingChange from baseline to post-assessment (after 10 weeks of training)Measured with the Delis-Kaplan Executive Functions System (D-KEFS) Color-Word Interference TestClinicalTrials.gov
OtherExecutive functioning: categorization and set-shiftingChange from baseline to post-assessment (after 10 weeks of training)Measured with D-KEFS Sorting TestClinicalTrials.gov
OtherTheory of mind reasoningChange from baseline to post-assessment (after 10 weeks of training)Measured with Hinting TaskClinicalTrials.gov
OtherMotivationThroughout the 10 weeks of trainingMeasured with the Intrinsic Motivation InventoryClinicalTrials.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
25379283BACKGROUNDPubMed

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 9

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
Digit Span TestPrimary outcomeConductCognition
Emotional Stroop TaskPrimary outcomeConductCognition
Matrix ReasoningPrimary outcomeConductCognition
Operation SpanPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Delay DiscountingOther outcomeConductCognition
Indirect Hints TaskOther 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)