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NCT03801382 · ClinicalTrials.gov registry record · NA

Psychometric Properties of IntelliSpace Cognition

A NA study, sponsored by Philips Electronics Nederland B.V. acting through Philips CTO organization.

Completed
Registry status
NA
Development phase
450
Enrollment target

NCT03801382: Completed NA study, sponsored by Philips Electronics Nederland B.V. acting through Philips CTO organization.

NCT03801382 is a NA study that has completed, run by Philips Electronics Nederland B.V. acting through Philips CTO organization. The registered enrollment target is 450 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03801382, a NA study, has completed, sponsored by Philips Electronics Nederland B.V. acting through Philips CTO organization.

COMPLETED
Registry status
NA
Development phase
450 participants
Enrollment target

Study Summary

This study aims to validate the tests that are on the IntelliSpace Cognition platform and to establish normative data for these tests.

Primary Outcome

Scores retrieved from all cognitive tests on the ISC platform The cognitive tests included on the ISC platform are commonly used in neuropsychological assessments and measure aspects of executive functioning (TMT A, TMT B, Star Cancellation Test, RAVLT, Letter Fluency Test, Category Fluency Test, ROCFT, Digit Span Forward, Digit Span Backward), processing speed (Star Cancellation Test), working memory (TMT A, TMT B, Star Cancellation Test, Letter Fluency Test, Digit Span Forward, Digit Span Back

Interventions

  • DEVICE IntelliSpace Cognition (ISC)
  • DIAGNOSTIC_TEST Paper-Pencil Tests

Trial Details

FieldValue
Enrollment Target 450 participants
Start Date 2019-04-15
Est. Completion 2019-08-26
Phase NA

What the finished NCT03801382 record still lists

NCT03801382 is an interventional study that assigns participants to a tested intervention. The registered 450 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 2 interventions - of which IntelliSpace Cognition (ISC) is the first listed.

NCT03801382 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03801382 about?

NCT03801382 is a clinical study titled "Psychometric Properties of IntelliSpace Cognition". This study aims to validate the tests that are on the IntelliSpace Cognition platform and to establish normative data for these tests.

What is the current status of trial NCT03801382?

This trial is currently completed. It is a NA study. The enrollment target is 450 participants. The study started on 2019-04-15. Estimated completion is 2019-08-26.

What interventions are being tested in trial NCT03801382?

The interventions under investigation include: IntelliSpace Cognition (ISC) (DEVICE), Paper-Pencil Tests (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT03801382?

This trial is sponsored by Philips Electronics Nederland B.V. acting through Philips CTO organization, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03801382's enrollment target sits among peer trials

450 225th of 2000 higher than 1,768 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03801382, the US trial registry maintained by the National Library of Medicine. NCT03801382 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.