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Evaluation of a Video-ludic Re-education of the Paretic Upper Limb in Chronic Hemipartic Patients Post Cerebral Vascular Accident (ERGOTACT)

C

Centre d'Investigation Clinique et Technologique 805

Status

Completed

Conditions

Stroke
Motor Activity

Treatments

Other: Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT03166020
2016-A01903-48

Details and patient eligibility

About

The aim of this randomized controlled study with stroke patients is to demonstrate that a re-education with interactive table with instrumented objects delivering sensory feedback and serious game improve certain motor functions of the paretic upper limb than rehabilitation based on a standardized self-rehabilitation program.

Enrollment

28 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Stroke patients
  • Subject with gripping ability: capable of peeling off the connected object from the table, presented in its grip area.

Exclusion criteria

  • Severe cognitive disorders preventing the completion of the task
  • Bilateral brain lesions

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

28 participants in 2 patient groups

Rehabilitation with Interactive Table
Experimental group
Description:
Included patients will be invited to participate in 10 sessions, focused on the movement and manipulation of instrumented objects on interactive table with serious game, during 30 minutes per day, 5 days a week, for 14 days. An occupational therapist will be required only for patient installation in front of the table.
Treatment:
Other: Rehabilitation
Self Rehabilitation
Active Comparator group
Description:
Included patients will be instructed to perform 10 self-rehabilitation sessions with 9 exercises (3 stretching, 3 reinforcement, 3 spot-oriented work) during 30 minutes per day, 5 days a week, for 14 days.
Treatment:
Other: Rehabilitation

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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