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NCT04119544Recruiting

Mirror Therapy Rehabilitation of the Upper Limb After Stroke (NEURO-MIROIR 2)

Intensive Rehabilitation Program With Intensive Visual Numerical Simulation Device for Improving Distal Motor Performance and Upper Limb Functional Capacity in Subacute Hemiparetics After Stroke. Randomized Controlled Trial.

Source: ClinicalTrials.gov · Last updated 18 Mar 2026

Brief summary (registry, in English)

Hemiparesis is a common motor disorder after a stroke. The majority of patients do not recover functional use of their paretic upper limb. The use of mirror therapy allows the activation of the mirror neurons involved to stimulate brain plasticity after brain damage.The IVS (Intensive Visual Stimulation) device allows an easy implementation of mirror therapy by filming the valid upper limb and projecting the inverted image onto a screen placed above the parietal arm thus producing the illusion of movement of the parietal arm. The main hypothesis of this study is that the structured practice of a large number of upper limb targeted movement repetitions using an intensive visual numerical simulation device as a partial replacement for routine care (conventional occupational therapy) in the sub-acute phase of stroke will increase the active function (motor function and functional abilities) of the distal end of the upper limb compared to conventional rehabilitation. Objectives: This randomized controlled trial will evaluate the effects of partial substitution of routine care (occupational therapy) by structured movement repetition programs by Intensive Visual Simulation using an IVS3 device, on the distal motor control of the upper hemiparesis limb, between 4 and 10 weeks after the stroke, compared to a program with conventional care alone.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
7 Oct 2019
Start date
10 Dec 2019
Primary completion date
31 Jul 2027
Lead sponsor
Clinique Les Trois Soleils
Diseases
Stroke
NCT number
NCT04119544

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 10 Dec 2019 to the primary completion date, 31 Jul 2027
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Neurological conditions prior to stroke
  • Patient who had mirror therapy or IVS rehabilitation before inclusion

Other illness

  • Cognitive dysfunction or progressive intercurrent illness making effective communication or participation in the study impossible
  • Phasic disorders that prevent the understanding of instructions

Other

  • Patient include in an other clinical trial
  • Rheumatological pathology of the hand and wrist
  • Person under legal protection measure.

Who the study is looking for

  • Age ≥18 years;
  • Stroke hemiparesis on unilateral focal lesion dating from 4 to 10 weeks at baseline;
  • Total sub-scores wrist and hand of th Fugl-Meyer \< 16
  • Patient having agreed to sign an informed consent
  • patient being affiliated to the French Social Security

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinique Les Trois Soleils
Coordinator of this site? Confirm its status
Boissise-le-RoiFranceRecruiting
CRF Pasori
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Cosne-Cours-sur-LoireFranceRecruiting
CHU Sébastopol
Coordinator of this site? Confirm its status
ReimsFranceNot yet recruiting
Clinique Napoléon
Coordinator of this site? Confirm its status
Saint-Paul-lès-DaxFranceNot yet recruiting
Clinalliance Villiers-sur Orge
Coordinator of this site? Confirm its status
Villiers-sur-OrgeFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.