Observational Study of 180° Turning Strategies Using Inertial Measurement Units and Fall Risk in Poststroke Hemiparetic Patients.
Rémi Pierre-Marie Barrois, Damien Ricard, Laurent Oudre...
https://pubmed.ncbi.nlm.nih.gov/28555124Actively Recruiting
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-05-27
40
Participants Needed
1
Research Sites
21 weeks
Total Duration
This research investigates balance rehabilitation in patients with acquired chronic demyelinating neuropathy who experience walking instability due to sensitivity disorders. The study aims to evaluate how modifying visual input during rehabilitation might reduce visual dependence and strengthen proprioceptive input, potentially improving balance and walking ability in these patients. This multicenter study is conducted in the Paris area and plans to include 40 participants. Participants are randomly assigned to one of two groups. The experimental group undergoes 20 rehabilitation sessions with a Physical Therapist, performing balance exercises while keeping their eyes closed or with vision obstructed or disturbed by visual effects in a dark room. The control group also receives 20 rehabilitation sessions but performs balance exercises with their eyes open and no visual modification. Both groups have three assessments during the study. Participants will undergo evaluations including timed U-turns at comfortable and fast speeds, number of steps, double stance phase while walking, global movement amounts, walking times and steps over 10 meters, various sensory and balance tests, and balance confidence scales. Assessments occur just after rehabilitation completion and again two months later. The primary outcome is the U-turn completion time measured shortly after the last session. The rehabilitation program spans 20 sessions with follow-up evaluations up to two months post-treatment.
CONDITIONS
Balance Rehabilitation With Modified Visual Input in Patients With Neuropathy
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 20 sessions over several weeks
Participants perform 20 rehabilitation sessions with a Physical Therapist. The experimental group will do balance training with modified visual input, while the control group performs balance training with no modified visual input.
20 rehabilitation sessions
Duration - Up to 2 months after treatment
Participants undergo assessments to evaluate balance and walking ability just after the rehabilitation program and again 2 months later.
3 assessment visits (shortly after treatment and at 2 months post-treatment)
Total: 1 location
1
Service de Médecine Physique et de Réadaptation (MPR)
Paris, France, 75010
Actively Recruiting
B
Bénédicte PANIGOT GUERIN, PT
A
Alain YELNIK, MD, PhD
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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