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Functionality and Neurocognition in Patients With Bipolar Disorder After a Physical-exercise Program (FINEXT-BD Study)

NCT04400630, Not applicable, Unknown, Bioaraba Health Research Institute

Trial 10

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

FieldValueSource
TitleFunctionality and Neurocognition in Patients With Bipolar Disorder After a Physical-exercise Program (FINEXT-BD Study)ClinicalTrials.gov
NCT numberNCT04400630ClinicalTrials.gov
StatusUnknownClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment80 participants, estimatedClinicalTrials.gov
Lead sponsorBioaraba Health Research InstituteClinicalTrials.gov
ConditionsBipolar DisorderClinicalTrials.gov
InterventionsPhysical exerciseClinicalTrials.gov
First posted2020-05-22ClinicalTrials.gov
Last updated2020-09-16ClinicalTrials.gov

Registered outcomes 64

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

ListOutcomeTime frameDescriptionSource
PrimaryPatient Functionality measured through the scale FAST (4 months)Change at the end of the training period (4 months)
The Functioning Assessment Short Test is a brief instrument designed to assess functional impairment in severe mental disorders. The 24 items of the scale cover six specific areas of functioning: autonomy, occupational functioning, cognitive functioning, financial issues, interpersonal relationships, and leisure time.
ClinicalTrials.gov
PrimaryPatient Functionality measured through the scale FAST (10 months)Changes after 10 months
The Functioning Assessment Short Test is a brief instrument designed to assess functional impairment in severe mental disorders. The 24 items of the scale cover six specific areas of functioning: autonomy, occupational functioning, cognitive functioning, financial issues, interpersonal relationships, and leisure time.
ClinicalTrials.gov
PrimaryPatient Functionality measured through the scale GAF (4 months)Change at the end of the training period (4 months)
Global Assessment of Functioning (GAF):This scale evaluates with a score from 0 to 100 the level of functioning and the severity of the patient's symptoms, the higher values corresponding to better overall functionality.
ClinicalTrials.gov
PrimaryPatient Functionality measured through the scale GAF (10 months)Changes after 10 months
Global Assessment of Functioning (GAF):This scale evaluates with a score from 0 to 100 the level of functioning and the severity of the patient's symptoms, the higher values corresponding to better overall functionality.
ClinicalTrials.gov
PrimaryPatient Functionality measured through the Strauss-Carpenter scale (4 months)Change at the end of the training period (4 months)
Strauss-Carpenter scale consists of four items rated from 0 to 4 on a Likert-type scale and yields a total score that is calculated by the addition of all item scores: the higher the score, the better is the prognosis.
ClinicalTrials.gov
PrimaryPatient Functionality measured through the Strauss-Carpenter scale (10) months)Changes after 10 months
Strauss-Carpenter scale consists of four items rated from 0 to 4 on a Likert-type scale and yields a total score that is calculated by the addition of all item scores: the higher the score, the better is the prognosis.
ClinicalTrials.gov
SecondaryTrkB-FL (4 months)Change at the end of the training period (4 months)Expression of BDNF: TrkB-FLClinicalTrials.gov
SecondaryTrkB-FL (10 months)Changes after 10 monthsExpression of BDNF: TrkB-FLClinicalTrials.gov
SecondaryTrkB-T (4 months)Change at the end of the training period (4 months)Expression of BDNF:TrkB-TClinicalTrials.gov
SecondaryTrkB-T (10 months)Changes after 10 monthsExpression of BDNF:TrkB-TClinicalTrials.gov
SecondaryBDNF (4 months)Change at the end of the training period (4 months)Peripheral BDNF levelsClinicalTrials.gov
SecondaryBDNF (10 months)Changes after 10 monthsPeripheral BDNF levelsClinicalTrials.gov
SecondaryPresence of depressive symptoms (4 months)Change at the end of the training period (4 months)Hamilton Depression Scale (HDRS-21)ClinicalTrials.gov
SecondaryPresence of depressive symptoms (10 months)Changes after 10 monthsHamilton Depression Scale (HDRS-21)ClinicalTrials.gov
SecondaryVO2Peak in CPET (4 months)Change at the end of the training period (4 months)Value of VO2Peak (L min-1) in cardiopulmonary exercise test (CPET)ClinicalTrials.gov
SecondaryVO2Peak in CPET (10 months)Changes after 10 monthsValue of VO2Peak (L min-1) in cardiopulmonary exercise test (CPET)ClinicalTrials.gov
SecondaryRelative VO2Peak in CPET (4 months)Change at the end of the training period (4 months)Value of relative VO2Peak (mL kg-1 min-1) in cardiopulmonary exercise test (CPET)ClinicalTrials.gov
SecondaryRelative VO2Peak in CPET (10 months)Changes after 10 monthsValue of relative VO2Peak (mL kg-1 min-1) in cardiopulmonary exercise test (CPET)ClinicalTrials.gov
SecondaryMETs in CPET (4 months)Change at the end of the training period (4 months)Value of metabolic equivalents in cardiopulmonary exercise test (CPET)ClinicalTrials.gov
SecondaryMETs in CPET (10 months)Changes after 10 monthsValue of metabolic equivalents in cardiopulmonary exercise test (CPET)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 1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
33240125DERIVEDPubMed

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
Card Sorting Test (Berg)Secondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition
Verbal LearningSecondary 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)