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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
Auxilium Vitae Volterra
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscle Spasticity focused on measuring Robotics, Upper Extremity

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Upper limb spasticity due to neurological impairment;
  2. Cognitive abilities sufficient for understanding instructions;
  3. Absence of severe pain assessed as Visual Analogic Score (VAS) < 4 (range 0-10).

Exclusion Criteria:

  1. Unstable general clinical conditions;
  2. Unability to keep sitting posture;
  3. 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

    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
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    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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