Tendon Vibrations Effect on Upper Limb Motor Recovery After Recent Stroke (VIBRAMOT)
Primary Purpose
Stroke/Brain Attack, Upper Extremity Paresis
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Upper limb repeated multi-site tendon vibrations
Sponsored by
About this trial
This is an interventional basic science trial for Stroke/Brain Attack focused on measuring stroke, rehabilitation, proprioception
Eligibility Criteria
Inclusion Criteria:
- 1st ischemic or hemorrhagic stroke
- Motor deficit of the upper limb (Fugl-Meyer between 0 and 50)
- Delay since stroke <or = 60 days
- Subject having given free and informed consent
- Subject affiliated to the social security system
Exclusion Criteria:
- Neurological history responsible for sensory or motor impairment of the concerned upper limb
- Surgical history concerning the nervous or locomotor system of the concerned upper limb
- Uncontrolled epilepsy
- Pace-maker
- Ferro-magnetic intra-cranial clip and any other contraindication to MEP and MRI
- Cochlear implants
- Pregnancy
- Guardianship or curatorship
Sites / Locations
- Physical and Rehabilitation Medicine department of Hôpital Fernand WidalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Experimental group (EG)
Control Group (CG)
Arm Description
An Experimental Group (EG) of post-stroke subjects having vibration stimulation sessions in addition to traditional rehabilitation
A Control Group (WG) of post-stroke subjects having placebo/sham vibration sessions (same vibrators used but without the eccentric mass), in addition to traditional rehabilitation
Outcomes
Primary Outcome Measures
Motor recovery assessment at the brain level by the efficiency of the primary motor pathway measured by Motor Evoked Potentials (MEP) recorded at the contralateral hand
Assessment of Motor recovery at the brain level by the efficiency of the primary motor pathway, measured by Motor Evoked Potentials (MEP) recorded at the contralateral hand:
Magnetic stimulation is provided on the motor cortex involved by the stroke. The MEP are recorded on the contralateral side on the hand interossei muscles, in a bandwidth of 20 to 1000 Hz.
The electromyographic activity is recorded continuously to ensure total relaxation of the patient before stimulation.
The main parameter recorded is:
the threshold defined by the minimum stimulation intensity capable of generating a MEP> 50 microvolts amplitude in at least 3 of 6 tests, while the muscle is fully relaxed. Same measurements are made after moderate contraction of the collecting muscles (finger spacing).
Secondary Outcome Measures
Motor recovery assessment at the upper limb level
Motor control effectiveness is measured by the Fugl Meyer scale, the Tardieu scale, the Action Research Arm Test (ARAT), the Box and Blocks Test (BBT) and the range of upper limb exploration with the ArmeoSpring (Hocoma)
To assess any impact on nerve fibers density on the main motor pathway by Magnetic Resonance Imaging
The MRI is used to assess the possible impact of vibrations on nerve fibers density of the main motor pathway (corticospinal bundle).
Diffusion tensor and tractography sequences are used to outline the direction and the density of nerve fibers. The corticospinal tract is particularly highlighted The first MRI takes place before any stimulation. It is used to localize the stroke in relation to the corticospinal tracts and to measure its volume.
A first tractography is used to assess the initial disorganization of the fiber bundles.
A 3D analysis of the tractography allows a visual assessment of the number and the density of fibers compared to the normal side.
A second MRI will be conducted after 3 months with same method of tractography analysis.
To test the feasibility of such a rehabilitation protocol in a PMR department
To study the impact of the protocol on the organization and rehabilitation if it proved useful to usual care.
The feasibility will be achieved by recording:
Total daily duration of installation and stimulation Technical difficulties encountered
Full Information
NCT ID
NCT04504214
First Posted
August 5, 2020
Last Updated
August 7, 2020
Sponsor
Centre Borelli UMR 9010
Collaborators
Hopital Lariboisière
1. Study Identification
Unique Protocol Identification Number
NCT04504214
Brief Title
Tendon Vibrations Effect on Upper Limb Motor Recovery After Recent Stroke
Acronym
VIBRAMOT
Official Title
A Pilot Study of Proprioception Stimulation by Repeated Multi-site Tendon Vibrations, on Upper Limb Motor Skills Recovery After Recent Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2015 (Actual)
Primary Completion Date
October 1, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre Borelli UMR 9010
Collaborators
Hopital Lariboisière
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Stroke is the leading cause of severe acquired disabilities in adults. It can affect sensory and motor functions which are closely entangled. Among them, upper limb function is often strongly impaired. In this study the investigators are interested in the eventuality to improve motor recovery by the mean of stimulating the proprioception.
Proprioception can be stimulated by tendinous vibrations in order to act on the neuromuscular system through the vibratory tonic reflex and by movement illusion.
Stimulation by tendinous vibrations, applied to the musculotendinous endings, has been already proposed in post stroke rehabilitation, but only at late stages. Thus the aim of our study is to observe the effects of repeated tendon vibrations, applied in the early post stroke phase, the effect being measured on the excitability of the motor cortex by the Motor Evoked Potentials and on the motor recovery (motor control and activities).
Detailed Description
Stroke is the leading cause of severe acquired disabilities in adults. It can affect sensory and motor functions which are closely entangled. Among them, upper limb function is often strongly impaired. In this study the investigators are interested in the eventuality to improve motor recovery by the mean of stimulating the proprioception.
Proprioception can be stimulated by tendinous vibrations in order to act on the neuromuscular system through the vibratory tonic reflex and by movement illusion.
Stimulation by tendinous vibrations, applied to the musculotendinous endings, has been already proposed in post stroke rehabilitation, but only at late stages.
Thus the aim of our study is to observe the effects of repeated tendon vibrations, applied in the early post stroke phase, the effect being measured on the excitability of the motor cortex by the Motor Evoked Potentials and on the motor recovery (motor control and activities).
Patients: 30 patients recruited after a first ever stroke whatever the cause and the site; age >18; stroke delay< 60 days; the maximum duration of participation for each patient is 3 months.
Protocol:
This rehabilitation protocol will be added to the usual rehabilitation program during inpatient rehabilitation.
Participants are randomized into two groups: experimental group and placebo group.
The experimental group benefits from upper limb tendon vibration sessions produced by small electromechanical vibrators on the elbow and the wrist. Frequency of the vibration is 80 Hz, two 15-minutes sessions per day scheduled for 10 days over a period of two weeks (2 x 5 days). During the sessions, the participant wearing opaque glasses, in a seating position, is asked to move if possible his/her arm in the opposite direction of the perceived movement.
The placebo group receives apparently the same treatment but with "sham" vibration.
Assessment:
Motor recovery will be assessed:
At the brain level by the efficiency of the primary motor pathway, measured by Motor Evoked Potentials recorded at the contralateral hand (main outcome criteria after 30 days from inclusion).
At the limb level by the motor control effectiveness measured by the Fugl Meyer scale, the Tardieu scale, the Action Research Arm Test (ARAT), the Box and Blocks Test (BBT) and the range of upper limb exploration with the ArmeoSpring, Hocoma brand.
The secondary objectives are:
To assess any impact on nerve fibers density on the main motor pathway by Magnetic Resonance Imaging.
To test the feasibility of such a rehabilitation protocol in a Physical Rehabilitation Medicine department
Four consultations are planned:
D0 (day 0): (before starting stimulation): Motor skills assessments, Motor Evoked Potentials (MEP) and Magnetic Resonance Imaging (MRI).
D15 (day 15): (as soon as stimulation ends): Motor skills assessments. D30 (day 30): Motor skills assessments and Motor Evoked Potentials (MEP) D90 (day 90): Motor skills assessments, Motor Evoked Potentials (MEP) and Magnetic Resonance Imaging (MRI).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke/Brain Attack, Upper Extremity Paresis
Keywords
stroke, rehabilitation, proprioception
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
pilot, prospective, biomedical, randomized, controlled study with intent-to-treat analysis of a stroke subjects cohort
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental group (EG)
Arm Type
Experimental
Arm Description
An Experimental Group (EG) of post-stroke subjects having vibration stimulation sessions in addition to traditional rehabilitation
Arm Title
Control Group (CG)
Arm Type
Sham Comparator
Arm Description
A Control Group (WG) of post-stroke subjects having placebo/sham vibration sessions (same vibrators used but without the eccentric mass), in addition to traditional rehabilitation
Intervention Type
Other
Intervention Name(s)
Upper limb repeated multi-site tendon vibrations
Intervention Description
Upper limb tendon vibration protocol will be added to the usual rehabilitation protocol performed during hospitalization
Primary Outcome Measure Information:
Title
Motor recovery assessment at the brain level by the efficiency of the primary motor pathway measured by Motor Evoked Potentials (MEP) recorded at the contralateral hand
Description
Assessment of Motor recovery at the brain level by the efficiency of the primary motor pathway, measured by Motor Evoked Potentials (MEP) recorded at the contralateral hand:
Magnetic stimulation is provided on the motor cortex involved by the stroke. The MEP are recorded on the contralateral side on the hand interossei muscles, in a bandwidth of 20 to 1000 Hz.
The electromyographic activity is recorded continuously to ensure total relaxation of the patient before stimulation.
The main parameter recorded is:
the threshold defined by the minimum stimulation intensity capable of generating a MEP> 50 microvolts amplitude in at least 3 of 6 tests, while the muscle is fully relaxed. Same measurements are made after moderate contraction of the collecting muscles (finger spacing).
Time Frame
30 day after the first assessment session (D30)
Secondary Outcome Measure Information:
Title
Motor recovery assessment at the upper limb level
Description
Motor control effectiveness is measured by the Fugl Meyer scale, the Tardieu scale, the Action Research Arm Test (ARAT), the Box and Blocks Test (BBT) and the range of upper limb exploration with the ArmeoSpring (Hocoma)
Time Frame
at inclusion (first assessment, D0), 15 days after inclusion (as soon as stimulations ends, D15), 30 days after inclusion (D30), 90 days after inclusion (D90)
Title
To assess any impact on nerve fibers density on the main motor pathway by Magnetic Resonance Imaging
Description
The MRI is used to assess the possible impact of vibrations on nerve fibers density of the main motor pathway (corticospinal bundle).
Diffusion tensor and tractography sequences are used to outline the direction and the density of nerve fibers. The corticospinal tract is particularly highlighted The first MRI takes place before any stimulation. It is used to localize the stroke in relation to the corticospinal tracts and to measure its volume.
A first tractography is used to assess the initial disorganization of the fiber bundles.
A 3D analysis of the tractography allows a visual assessment of the number and the density of fibers compared to the normal side.
A second MRI will be conducted after 3 months with same method of tractography analysis.
Time Frame
at inclusion (first assessment, D0), 90 days after inclusion (D90)
Title
To test the feasibility of such a rehabilitation protocol in a PMR department
Description
To study the impact of the protocol on the organization and rehabilitation if it proved useful to usual care.
The feasibility will be achieved by recording:
Total daily duration of installation and stimulation Technical difficulties encountered
Time Frame
After inclusions completion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1st ischemic or hemorrhagic stroke
Motor deficit of the upper limb (Fugl-Meyer between 0 and 50)
Delay since stroke <or = 60 days
Subject having given free and informed consent
Subject affiliated to the social security system
Exclusion Criteria:
Neurological history responsible for sensory or motor impairment of the concerned upper limb
Surgical history concerning the nervous or locomotor system of the concerned upper limb
Uncontrolled epilepsy
Pace-maker
Ferro-magnetic intra-cranial clip and any other contraindication to MEP and MRI
Cochlear implants
Pregnancy
Guardianship or curatorship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emna JELILI, engineer
Phone
+33 (0) 1 40 05 49 46
Email
emna.jelili@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Marylène JOUSSE, MD, PhD
Email
marylene.jousse@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alain YELNIK, MD, Prof
Organizational Affiliation
Centre BORELLI
Official's Role
Study Director
Facility Information:
Facility Name
Physical and Rehabilitation Medicine department of Hôpital Fernand Widal
City
Paris
State/Province
Île De France
ZIP/Postal Code
75010
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emna JELILI, engineer
Phone
+33 (0) 1 40 05 49 46
Email
emna.jelili@aphp.fr
First Name & Middle Initial & Last Name & Degree
Marylène JOUSSE, MD, PhD
Email
marylene.jousse@aphp.fr
First Name & Middle Initial & Last Name & Degree
Alain YELNIK, MD, Prof
First Name & Middle Initial & Last Name & Degree
Marylène JOUSSE, MD, PhD
First Name & Middle Initial & Last Name & Degree
Nathtalie KUBIS, MD, Prof
First Name & Middle Initial & Last Name & Degree
Jean Pierre GUICHARD, MD
First Name & Middle Initial & Last Name & Degree
Emna JELILI, Engineer
12. IPD Sharing Statement
Plan to Share IPD
No
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Links:
URL
https://www.santepubliquefrance.fr/maladies-et-traumatismes/maladies-cardiovasculaires-et-accident-vasculaire-cerebral/accident-vasculaire-cerebral
Description
epidemiological stroke data in France
Learn more about this trial
Tendon Vibrations Effect on Upper Limb Motor Recovery After Recent Stroke
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