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Trial · NCT04731246

Video-oculography and Parkinson's Disease

NCT04731246, Not applicable, Recruiting, Association de Recherche Bibliographique pour les Neurosciences

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Video-oculography and Parkinson's Disease. Trials, record NCT04731246. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04731246

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Trial

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

Title
Video-oculography and Parkinson's Disease
NCT number
NCT04731246
Status
Recruiting
Phases
Not applicable
Enrollment
30 participants, estimated
Lead sponsor
Association de Recherche Bibliographique pour les Neurosciences
Conditions
Parkinson Disease, Idiopathic
Interventions
Video-oculography / Neuropsychological evaluations
First posted
2021-01-29
Last updated
2026-10-13

Source ClinicalTrials.gov

Registered outcomes41

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

ListOutcomeTime frameDescription
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Latency in Horizontal saccades.Baseline; Year 7
This concerns saccades Latency (in ms) during horizontal paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Main velocity in Horizontal saccades.Baseline; Year 7
This concerns saccades Main velocity (in °/sec) during horizontal paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Gain in Horizontal saccades.Baseline; Year 7
This concerns saccades Gain (gaze accuracy) during horizontal paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Latency in Vertical saccades.Baseline; Year 7
This concerns saccades Latency (in ms) during vertical paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Main velocity in Vertical saccades.Baseline; Year 7
This concerns saccades Main velocity (in °/sec) during vertical paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Oculomotor raw performance at 7 years - Gain in Vertical saccades.Baseline; Year 7
This concerns saccades Gain (gaze accuracy) during vertical paradigms. Eye movements were recorded and analyzed with an eye-tracking device. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Inhibition capacity at 7 yearsBaseline; Year 7
Measure of inhibition capacity performance during an "antisaccades" paradigm. Eye movements were recorded and analyzed with an eye-tracking device. Evaluation criteria: percentage of errors. For each subject value were judged abnormal if they differed by \>1.65 SD compared to their reference sample.
PrimaryChange from Baseline of Internuclear ophthalmoplegia (INO) detection at 7 yearsBaseline; Year 7
Highlight presence/absence of INO. Eye movements were recorded and analyzed with an eye-tracking device. Evaluation criteria: INO is present if calculated ratio of abducting to adducting eye movement (both mean and peak velocity) is \>1.
PrimaryChange from Baseline of Fixations impairments detection at 7 yearsBaseline; Year 7
Highlight presence/absence of Fixations impairments. Eye movements were recorded and analyzed with an eye-tracking device. Evaluation criteria: presence/absence/frequency of square wave-jerks, nystagmus, flutters.
SecondaryPatients descriptionBaselineProfile description of included patients, based on demographic data and clinical exam (sex, age, Weight, height), inclusion/exclusion criteria, medical history, concomitant treatments.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

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.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests8

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

TestNamed asSource
Antisaccade TaskPrimary outcomeConductCognition
Category FluencySecondary outcomeConductCognition
Emoji Emotion RecognitionSecondary outcomeConductCognition
Social Slips Stories TaskSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition
Verbal FluencySecondary outcomeConductCognition

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04731246

GET https://conductscience.org/api/trials/v1/NCT04731246/registered?page=2