Powered Exoskeleton for the Treatment of Elbow Spasticity
Primary Purpose
Muscle Spasticity, Stroke
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Robotic treatment
Sponsored by
About this trial
This is an interventional treatment trial for Muscle Spasticity focused on measuring Robotics, Upper Extremity
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;
- Unability to keep sitting posture;
- Tendon retractions limiting upper limb joints range of motion.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Subacute stroke patients
Arm Description
Elbow passive/active robotic treatment provided by NEUROExos Elbow Module
Outcomes
Primary Outcome Measures
Modified Ashworth Scale
Impairmente level maesure according to ICF
Secondary Outcome Measures
Range of Motion
Impairmente level maesure according to ICF
Maximum Extension Torque
Paramenter directly exterted by the device
Zero-Torque Angle
Paramenter directly exterted by the device
Full Information
NCT ID
NCT02934646
First Posted
October 12, 2016
Last Updated
July 24, 2018
Sponsor
Auxilium Vitae Volterra
Collaborators
Azienda USL Toscana Nord Ovest, Scuola Superiore Sant'Anna di Pisa
1. Study Identification
Unique Protocol Identification Number
NCT02934646
Brief Title
Powered Exoskeleton for the Treatment of Elbow Spasticity
Official Title
Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity: Phase II Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Auxilium Vitae Volterra
Collaborators
Azienda USL Toscana Nord Ovest, Scuola Superiore Sant'Anna di Pisa
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a phase-II clinical study to assess whether intense passive mobilization of the elbow during the early stage is effective in preventing spasticity from occurring at a later stage. A group of subacute stroke patients was treated with the device named NEUROExos Elbow Module (NEEM) on a daily basis, in addition to traditional physical therapy. The outcome was assessed in terms of (i) system safety, (ii) system usability and (iii) treatment efficacy.
Investigators expected that intense therapy performed in the sub-acute phase following the stroke would be effective in preventing elbow spasticity from occurring at a later stage (i.e. 3-4 months after the stroke), the latter being quantified by means of the Modified Ashworth Scale (MAS). Similarly to other phase-II studies in the field of post-stroke rehabilitation, the present study will include only one group of patients. As a secondary objective, similarly to other studies with robot-assisted therapy, investigators wiil test the ability of this system to be used for assessing rehabilitation outcome. Investigators will introduce novel evaluation metrics based on the kinematics and kinetics variables recorded by the NEEM and compared them with MAS values.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Spasticity, Stroke
Keywords
Robotics, Upper Extremity
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Subacute stroke patients
Arm Type
Experimental
Arm Description
Elbow passive/active robotic treatment provided by NEUROExos Elbow Module
Intervention Type
Device
Intervention Name(s)
Robotic treatment
Intervention Description
Passive/active elbow mobilizzation provided by NEUROExos Elbow Module Robotic device
Primary Outcome Measure Information:
Title
Modified Ashworth Scale
Description
Impairmente level maesure according to ICF
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Range of Motion
Description
Impairmente level maesure according to ICF
Time Frame
2 weeks
Title
Maximum Extension Torque
Description
Paramenter directly exterted by the device
Time Frame
2 weeks
Title
Zero-Torque Angle
Description
Paramenter directly exterted by the device
Time Frame
2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 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;
Unability to keep sitting posture;
Tendon retractions limiting upper limb joints range of motion.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Powered Exoskeleton for the Treatment of Elbow Spasticity
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