Multimodal Instrumented Assessment of Post-stroke Elbow
Primary Purpose
Spasticity, Muscle, Stroke, Upper Limb
Status
Enrolling by invitation
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Neuroexsos elbow module
Sponsored by
About this trial
This is an interventional treatment trial for Spasticity, Muscle focused on measuring Robotics, Upper extremities, EMG
Eligibility Criteria
Inclusion Criteria:
- Upper limb spasticity due to neurological impairment;
- Cognitive abilities sufficient for understanding instructions;
- Absence of severe pain assessed as Visual Analogic Score (VAS) < 4 (range 0-10).
Exclusion Criteria:
- Unstable general clinical conditions;
- Inability to keep sitting posture;
- Tendon retractions limiting upper limb joints range of motion.
Sites / Locations
- Ospedale Versilia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Robotic treatment
Conventional treatment
Arm Description
Patients receive 4 weeks of elbow rehabilitation treatment provided by the NEEM robotic elbow exoskeleton
Patients receive 4 weeks of elbow conventional rehabilitation treatment matched in time
Outcomes
Primary Outcome Measures
Change in the score of the upper-extremity section of Fugl-Meyer assessment scale (FM 0-66) higher score means better
It is a clinical scale used for the assessment of motor function in stroke patients
Change in the score of Modified Ashworth Scale (MAS 0-5 scoring 1+ as 2 for statistical analysis) higher score means worse
It is a clinical scale for spasticity assessment
Secondary Outcome Measures
Change in Maximum Extension Torque (MET)
It corresponds to the maximum torque value recorded during a static hold phase at the maximum reached extension angle
Change in Zero Torque Angle (ZTA)
It is the angular value corresponding to null torque exerted by the robot; in this configuration, flexor and extensor torques are equal and opposite and the system is ideally not applying any force to hold the elbow in position, which has reached its equilibrium point
Change in Joint Impedance (JIMP)
A measure of the limb resistance to muscle elongation, extracted as the ratio between joint torque and joint angular position for constant, slow-speed movements, the main contribution to the joint impedance can be identified in the joint stiffness (i.e. rigidity).
Full Information
NCT ID
NCT04484571
First Posted
July 10, 2020
Last Updated
July 22, 2023
Sponsor
Azienda USL Toscana Nord Ovest
Collaborators
Scuola Superiore Sant'Anna Pisa
1. Study Identification
Unique Protocol Identification Number
NCT04484571
Brief Title
Multimodal Instrumented Assessment of Post-stroke Elbow
Official Title
Robotic Rehabilitation and Multimodal Instrumented Assessment of Post-stroke Elbow Motor Functions - a Randomized Controlled Trial Protocol
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
July 6, 2020 (Actual)
Primary Completion Date
May 30, 2024 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda USL Toscana Nord Ovest
Collaborators
Scuola Superiore Sant'Anna Pisa
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The proposed clinical trial will employ the NEUROExos Elbow Module (NEEM), an active robotic exoskeleton, for the passive mobilization and active training of elbow flexion and extension in 60 sub-acute and chronic stroke patients with motor impairments (hemiparesis and/or spasticity) of the right arm. The study protocol is a randomized controlled trial consisting of a 4-week functional rehabilitation program, with both clinical and robotically instrumented assessments to be conducted at baseline and post-treatment.
Detailed Description
The reliable assessment, attribution, and alleviation of upper-limb joint stiffness are essential clinical objectives in the early rehabilitation from stroke and other neurological disorders, to prevent the progression of neuromuscular pathology and enable proactive physiotherapy towards functional recovery. However, the current clinical evaluation and treatment of this stiffness (and underlying muscle spasticity) are severely limited by their dependence on subjective evaluation and manual limb mobilization, thus rendering the evaluation imprecise and the treatment insufficiently tailored to the specific pathologies and residual capabilities of individual patients. To address these needs, the proposed clinical trial will employ the NEUROExos Elbow Module (NEEM), an active robotic exoskeleton, for the passive mobilization and active training of elbow flexion and extension in stroke patients with motor impairments (hemiparesis and/or spasticity) of the right arm. The study protocol provide a functional rehabilitation program, with both clinical and robotically instrumented assessments to be conducted at baseline and post-treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spasticity, Muscle, Stroke, Upper Limb
Keywords
Robotics, Upper extremities, EMG
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized Clinical Trial
Masking
Outcomes Assessor
Masking Description
Indipendent assessor blinded on treatment provided
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Robotic treatment
Arm Type
Experimental
Arm Description
Patients receive 4 weeks of elbow rehabilitation treatment provided by the NEEM robotic elbow exoskeleton
Arm Title
Conventional treatment
Arm Type
Active Comparator
Arm Description
Patients receive 4 weeks of elbow conventional rehabilitation treatment matched in time
Intervention Type
Device
Intervention Name(s)
Neuroexsos elbow module
Intervention Description
The treatment group will be further divided into two levels (sub-groups), based on pathological severity: Level 1 corresponds to an FM score equal or below 28, and Level 2 with FM greater than 28. The two sub-groups will receive different combinations of robotically assisted passive mobilization (PM) and active mobilization (AM) treatment modalities, according to their differing clinical needs
Primary Outcome Measure Information:
Title
Change in the score of the upper-extremity section of Fugl-Meyer assessment scale (FM 0-66) higher score means better
Description
It is a clinical scale used for the assessment of motor function in stroke patients
Time Frame
before and within 1 week after 4 weeks of treatment
Title
Change in the score of Modified Ashworth Scale (MAS 0-5 scoring 1+ as 2 for statistical analysis) higher score means worse
Description
It is a clinical scale for spasticity assessment
Time Frame
Before and within 1 week after 4 weeks of treatment
Secondary Outcome Measure Information:
Title
Change in Maximum Extension Torque (MET)
Description
It corresponds to the maximum torque value recorded during a static hold phase at the maximum reached extension angle
Time Frame
Before and within 1 week after 4 weeks of treatment
Title
Change in Zero Torque Angle (ZTA)
Description
It is the angular value corresponding to null torque exerted by the robot; in this configuration, flexor and extensor torques are equal and opposite and the system is ideally not applying any force to hold the elbow in position, which has reached its equilibrium point
Time Frame
Before and within 1 week after 4 weeks of treatment
Title
Change in Joint Impedance (JIMP)
Description
A measure of the limb resistance to muscle elongation, extracted as the ratio between joint torque and joint angular position for constant, slow-speed movements, the main contribution to the joint impedance can be identified in the joint stiffness (i.e. rigidity).
Time Frame
Before and within 1 week after 4 weeks of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Upper limb spasticity due to neurological impairment;
Cognitive abilities sufficient for understanding instructions;
Absence of severe pain assessed as Visual Analogic Score (VAS) < 4 (range 0-10).
Exclusion Criteria:
Unstable general clinical conditions;
Inability to keep sitting posture;
Tendon retractions limiting upper limb joints range of motion.
Facility Information:
Facility Name
Ospedale Versilia
City
Camaiore
State/Province
Lucca
ZIP/Postal Code
55041
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33193052
Citation
Pilla A, Trigili E, McKinney Z, Fanciullacci C, Malasoma C, Posteraro F, Crea S, Vitiello N. Robotic Rehabilitation and Multimodal Instrumented Assessment of Post-stroke Elbow Motor Functions-A Randomized Controlled Trial Protocol. Front Neurol. 2020 Oct 22;11:587293. doi: 10.3389/fneur.2020.587293. eCollection 2020.
Results Reference
derived
Learn more about this trial
Multimodal Instrumented Assessment of Post-stroke Elbow
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