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NCT04403464

Effect of a New Interactive Device on the Motor and Functional Abilities of Children With Bilateral Cerebral Palsy

Status unknown NA Last updated 15 June 2022
What this trial tests

NA trial testing HABIT-ILE with REAtouch® in Cerebral Palsy in 30 participants. Status unknown.

Timeline
26 May 2020
Primary endpoint
20 November 2022
20 December 2022

Quick facts

Lead sponsorUniversité Catholique de Louvain
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment30
Start date26 May 2020
Primary completion20 November 2022
Estimated completion20 December 2022
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Université Catholique de Louvain — full company profile →

Who can join

Adults 5 to 18, any sex, with Cerebral Palsy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Recent research has shown that interventions with assistive technologies lead to an improvement in the motor and functional abilities of children with cerebral palsy (CP). REAtouch® is a new interactive interface based on motor skill learning principles. Its efficiency during intensive motor skill learning interventions has never been tested in children with bilateral cerebral palsy. Therefore, the study aims to investigate the efficiency of using a virtual reality tool to provide a motor skill learning intervention in a randomized trial.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cerebral Palsy

Currently open trials in the same condition.

Other Université Catholique de Louvain trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04403464.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing