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Neuropsychiatry and Cognition in SCA3/MJD

NCT04714307, Unknown, Hospital de Clinicas de Porto Alegre

Trial 9

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

FieldValueSource
TitleNeuropsychiatry and Cognition in SCA3/MJDClinicalTrials.gov
NCT numberNCT04714307ClinicalTrials.gov
StatusUnknownClinicalTrials.gov
Enrollment144 participants, estimatedClinicalTrials.gov
Lead sponsorHospital de Clinicas de Porto AlegreClinicalTrials.gov
ConditionsSpinocerebellar Ataxia Type 3, Machado-Joseph Disease, SCA3, MJDClinicalTrials.gov
InterventionsSCA3/MJD molecular diagnosis, Cognitive Testing, Psychiatric Evaluation, Clinical Neurological Evaluation, Emotional Attribution Evaluation, Activities of Daily LivingClinicalTrials.gov
First posted2021-01-19ClinicalTrials.gov
Last updated2021-01-19ClinicalTrials.gov

Registered outcomes 11

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

ListOutcomeTime frameDescriptionSource
PrimaryCerebellar Cognitive Affective Syndrome ScaleThrough study completion, an average of 1 year
Study the performance on the Cerebellar Cognitive Affective Syndrome Scale of SCA3/MJD symptomatic subjects when compared to matched healthy controls and of pre-symptomatic subjects when compared to familial healthy controls.
ClinicalTrials.gov
PrimaryTrail-Making Test Part A and BThrough study completion, an average of 1 year
Study the performance on the Trail-Making Test Part A and B of SCA3/MJD symptomatic subjects when compared to matched healthy controls and of pre-symptomatic subjects when compared to familial healthy controls.
ClinicalTrials.gov
PrimaryStroop Color-Word TestThrough study completion, an average of 1 year
Study the performance on the Stroop Color-Word Test of SCA3/MJD symptomatic subjects when compared to matched healthy controls and of pre-symptomatic subjects when compared to familial healthy controls.
ClinicalTrials.gov
PrimaryEmotion Attribution impairment in SCA3/MJDThrough study completion, an average of 1 yearStudy the performance of symptomatic SCA3/MJD carriers in the Reading the Mind in the Eyes Test.ClinicalTrials.gov
PrimaryEmotion Attribution in different phases of the diseaseThrough study completion, an average of 1 yearStudy the performance of pre-symptomatic SCA3/MJD carriers in the Reading the Mind in the Eyes Test.ClinicalTrials.gov
PrimaryHamilton Anxiety Rating ScaleThrough study completion, an average of 1 yearStudy the profile of symptomatic and pre-symptomatic SCA3/MJD carriers in the Hamilton Anxiety Rating Scale.ClinicalTrials.gov
PrimaryHamilton Depression Rating ScaleThrough study completion, an average of 1 yearStudy the profile of symptomatic and pre-symptomatic SCA3/MJD carriers in the Hamilton Depression Rating Scale.ClinicalTrials.gov
SecondaryScale for the Assessment and Rating of Ataxia (SARA)Through study completion, an average of 1 yearCorrelations between primary outcomes and SARA.ClinicalTrials.gov
SecondaryComposite Cerebellar Functional Severity Score (CCFS)Through study completion, an average of 1 yearCorrelations between primary outcomes and CCFS.ClinicalTrials.gov
SecondarySCA Functional IndexThrough study completion, an average of 1 yearCorrelations between primary outcomes and SCAFI.ClinicalTrials.gov
SecondaryFriedreich Ataxia Rating Scale part II (FARS part II)Through study completion, an average of 1 yearCorrelations between primary outcomes and Activities of Daily Living from FARS part II.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 2

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

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)