Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT03881930

Balance Rehabilitation With Modified Visual Input in Patients With Neuropathy

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2024-07-03

40

Participants Needed

1

Research Sites

334 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on the effects of rehabilitation on balance, in patients with acquired chronic demyelinating neuropathy. Rehabilitation will be performed with or without vision. It is planned to include 40 subjects consulting for walking instability related to sensitivity disorders. This multicenter study will take place in Paris's area. Each participant will benefit from 20 rehabilitation sessions with a Physical Therapist and 3 assessments. Thanks to randomization, patient will be allocated in one of the 2 following groups: * Control group, Patients will benefit from balance rehabilitation with open eyes. * Experimental group, they will perform the same exercises while keeping their eyes closed or their vision will be obstructed by a mask or disturbed by moving luminous dots projected on the environment in darkness.

CONDITIONS

Official Title

Balance Rehabilitation With Modified Visual Input in Patients With Neuropathy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with chronic demyelinating acquired neuropathy
  • Age 18 years or older
  • Able to walk 20 meters indoors without human assistance, with or without technical aid
  • Complaints of discomfort or walking instability related to sensitivity disorders
  • Clinically stable for at least 2 months, regardless of treatment
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Unable to walk 20 meters indoors without both technical and human assistance
  • Currently hospitalized
  • Participating in another intervention study
  • Undergoing ongoing balance rehabilitation in another center during this program
  • Receiving acute treatment for polyneuropathy started or stopped less than 2 months ago
  • Scheduled surgery during study participation preventing completion of rehabilitation and assessments
  • Recent surgery or lower limb prosthesis less than 1 year old
  • Skin wounds on the foot preventing rehabilitation
  • Balance disorders from vestibular or central neurological causes
  • Visual disability
  • Hearing impairment preventing understanding instructions
  • Unable to speak or understand French
  • Cognitive or language impairments preventing protocol understanding
  • Resident outside Paris Region (Ile de France)
  • Known pregnancy
  • Not affiliated with social security, under guardianship, or prisoner

AI-Screening

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Trial Site Locations

Total: 1 location

1

Service de Médecine Physique et de Réadaptation (MPR)

Paris, France, 75010

Actively Recruiting

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Research Team

B

Bénédicte PANIGOT GUERIN, PT

CONTACT

A

Alain YELNIK, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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