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Post-stroke Haptic Feedback Use Deficit: A Comparative and Reliability Study

NCT06344221 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2024-04-03

No results posted yet for this study

Summary

The aim of this comparative and reliability study is to highlight a deficit in the use of vibrotactile sensory feedback (haptic effect) in the planning and execution of fine manual dexterity movements after stroke. The investigators will include 3 groups of subjects, 1 group of young healthy subjects, 1 of older subjects matched in age and sex to the group of chronic stroke patients. Participants will take part in clinical tests of fine motor skills and sensitivity and will use a device to assess the key components of manual dexterity, to which vibrotactile sensors will be added. If they so wish, participants will be able to take part in a transcranial magnetic stimulation (TMS) study to assess the facilitation of cortical excitability due to the haptic effect.

Conditions

  • Stroke
  • Upper Extremity Paresis
  • Manual Dexterity
  • Sensory Integration Dysfunction
  • Vibration; Disorder

Interventions

DEVICE

Dextrain Manipulandum and haptic feedback device

Assessment of key components of manual dexterity in addition to vibrotactile stimulation on the fingers and wrist.

Sponsors & Collaborators

  • Paris Brain Institute (ICM)

    collaborator OTHER

  • Centre Hospitalier Régional d'Orléans

    collaborator OTHER

  • Centre Hospitalier St Anne

    lead OTHER

Principal Investigators

  • Guillaume Turc · GHU Psychiatrie et Neurosciences de Paris

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-04-15
Primary Completion
2024-07-15
Completion
2024-07-15

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06344221 on ClinicalTrials.gov