Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05902910

Efficacy and Acceptability of the Luna EMG Rehabilitation Robot on Motor Recovery of the Upper Limb in the Chronic Phase of Stroke

Led by University Hospital, Brest · Updated on 2025-06-24

5

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Brest

Lead Sponsor

E

EGZOTech

Collaborating Sponsor

AI-Summary

What this Trial Is About

Recent work on large cohorts of chronic stroke (\>6 months post-stroke) have shown that intensive training of the upper limb in the chronic stroke patients can lead to substantial motor and functional gains that are maintained at 6 months post intervention. A very prolonged (12 weeks) and very intensive (5 hours daily) training applied to chronic patients after stroke brings a substantial gain both motor and functional which is maintained at 3 months post intervention. Robotic rehabilitation have been shown to be as effective as any other treatment used in rehabilitation. But the methods of implementation remain widely debated. At that time, most robotic therapies have tried to reproduce functional movement mainly pointing objects. We want to demonstrate that analytic movements of the elbow and the shoulder performed with the Luna-EMG robot can replace part of usual physiotherapy treatment with at least the same effectiveness on the recovery of fluid movements of the upper limb after a stroke.

CONDITIONS

Official Title

Efficacy and Acceptability of the Luna EMG Rehabilitation Robot on Motor Recovery of the Upper Limb in the Chronic Phase of Stroke

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age �318 years
  • Hemiparesis after a first stroke with more than 1 year time interval
  • Functional upper limb: ability to do a pointing task at 90% of the hand-acromion distance (free trunk)
  • Spastic hypertonia of the elbow flexors 0-2/4 on the Modified Ashworth scale
  • Patient affiliated with social security
  • Patient having signed a consent to participate in the research
Not Eligible

You will not qualify if you...

  • Inability to sign written consent
  • Flexed elbow > 30�b0 during passive mobilization of the upper limb
  • EVA > 3 in the upper limb at rest or during mobilization
  • Complete loss of upper limb proprioception
  • Neuro-orthopedic surgery of the upper limb for spasticity: neurotomy, tenotomy, transfer
  • Pregnant or breastfeeding woman

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Brest

Brest, France, 29200

Actively Recruiting

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Research Team

O

Olivier Remy-Neris, PU-PH

CONTACT

G

Gwenaël Cornec, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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