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Hand Motor Rehabilitation Using a Wearable Robotic Device (WRL HX MCP)

Primary Purpose

Hand Injuries

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
WRL HX MCP
Sponsored by
Istituto Nazionale Assicurazione contro gli Infortuni sul Lavoro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Hand Injuries focused on measuring Humans, Adult, Diseases, musculoskeletal, Metacarpophalangeal Joints, Range of Motion, Articular, Feasibility Studies, Rehabilitation Research, Robotics, Exoskeleton Device, Wearable Electronic Devices

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • history of traumatic hand injury or post-traumatic hand surgery
  • hand size allowing to achieve proper exoskeleton fit
  • NRS pain score in the 1-5 range

Exclusion Criteria:

  • cognitive or linguistic ability insufficient to understand instructions
  • cardiac implanted electronic devices
  • open skin at the level of the patient-device interface
  • absence of contraindications for finger joints mobilisation
  • current or prior history of malignancy
  • pregnancy or breast feeding

Sites / Locations

  • INAIL - Centro di Riabilitazione Motoria di VolterraRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Robotic therapy

Arm Description

All participants will receive a program of robot-assisted rehabilitation exercises., including passive, active-assisive and active MCP Range-of-Motion Exercises, and active bidigital pinching movements in the transparent mode.

Outcomes

Primary Outcome Measures

Feasibility indicator: completion of study procedures
Percent of participants for whom study procedures were completed successfully
Feasibility indicator: patient acceptability
Clinician-generated questionnaire to investigate patients' impressions about the physical interaction with the robotic device
Feasibility indicator: reliability evaluated through the number of device malfunctions
The physiotherapist is required to report any malfunctions occurring during the study in regard to the use of WRL HX MCP

Secondary Outcome Measures

Goniometric measure of MCP Active Range of Motion (AROM)
The physiotherapist measures the MCP joint angles in maximum active flexion and extension using a short-arm goniometer
Goniometric measure of MCP Passive Range of Motion (PROM)
The physiotherapist measures the MCP joint angles in maximum passive flexion and extension using a short-arm goniometer
Robotic measure of MCP Active Range of Motion (AROM)
MCP joint maximum active flexion and extension range of motion is registered while the device and human joint are coupled together, using WRL HX MCP set in a transparent mode as an evaluation tool, without any manual assistance.
Robotic measure of MCP passive Range of Motion (PROM)
MCP joint maximum passive flexion and extension range of motion is registered while the device and human joint are coupled together, using WRL HX MCP set in a transparent mode as an evaluation tool, with manual assistance from the therapist.
Robotic estimation of MCP joint flexion peak torque
MCP joint flexion peak torque is evaluated by the exoskeleton torque joint sensor during the robot-in-charge mobilization sequences
Numeric Pain Rating Scale (NPRS)
NPRS is an 11-point scale for patient self-reporting of pain, with 0 being "no pain" and 10 being "the worst pain imaginable"
Safety evaluated through the number of adverse events
The physiotherapist is required to report any adverse events occurring during the study in regard to the use of WRL HX MCP

Full Information

First Posted
November 21, 2021
Last Updated
August 2, 2022
Sponsor
Istituto Nazionale Assicurazione contro gli Infortuni sul Lavoro
Collaborators
Scuola Superiore Sant'Anna di Pisa
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1. Study Identification

Unique Protocol Identification Number
NCT05155670
Brief Title
Hand Motor Rehabilitation Using a Wearable Robotic Device (WRL HX MCP)
Official Title
Hand Motor Rehabilitation Using a Wearable Robotic Device (WRL HX MCP): a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
March 26, 2021 (Actual)
Primary Completion Date
September 25, 2022 (Anticipated)
Study Completion Date
September 25, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Nazionale Assicurazione contro gli Infortuni sul Lavoro
Collaborators
Scuola Superiore Sant'Anna di Pisa

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
The purpose of this pilot study is to assess the safety and usability of the WRL HX MCP medical device, a prototypal robotic system for metacarpophalangeal joint mobilization. WRL HX MCP was developed by the Wearable Robotics Laboratory of Scuola Superiore Sant'Anna in a project funded by and in collaboration with INAIL, to fulfil the needs of patients with post-traumatic hand stiffness.
Detailed Description
This study aims to: Test the safety and reliability of the WRL HX MCP device for assisting flexion and extension movement of the stiff metacarpophalangeal joint Conduct a preliminary examination of the efficacy of the device in the treatment of joint stiffness to design a subsequent RCT Evaluate the performance of the device in estimating the biomechanical parameters useful for the objective treatment outcome assessment. Ten injured workers with post-traumatic and/or post-operative index finger MCP stiffness will be enrolled in a clinical trial consisting of one to four sessions of robotic therapy with WRL HX MCP at the INAIL Rehabilitation Center in Volterra. Pilot testing of the experimental device will include the preliminary goniometric measure of passive and active MCP range of motion (ROM), the selection of the appropriate size of exoskeleton segments to fit user's anthropometry, the robotic assessment of ROM, force and torque trajectories of MCP joint, a program of robot-assisted passive and active MCF mobilization and a final clinical and robotic reassessment of joint ROM. The session will last about 1 hour and all exercises will be administered by a trained physical therapist supported by two members of the engineering team; pain level will be assessed at baseline and after each mobilization sequence; patient feedback will be recorded about the usability of the device in term of comfort, wearability, user safety, and overall satisfaction. For Aim 1, the Safety and Reliability of the device will be evaluated in terms of the number of adverse events and malfunctions occurring during the study session. For Aim 2, the efficacy of robot-assisted mobilization modes will be assessed by means of the longitudinal analysis of pre- and post-treatment measurements of MCP range of motion and pain intensity level, the flexion peak torque evaluation and the final administration of an ad-hoc satisfaction questionnaire. For aim 3, the performance of WRL HX MCP will be studied by comparing the robotic MCP angle estimation with the measurements from a motion capture system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hand Injuries
Keywords
Humans, Adult, Diseases, musculoskeletal, Metacarpophalangeal Joints, Range of Motion, Articular, Feasibility Studies, Rehabilitation Research, Robotics, Exoskeleton Device, Wearable Electronic Devices

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robotic therapy
Arm Type
Experimental
Arm Description
All participants will receive a program of robot-assisted rehabilitation exercises., including passive, active-assisive and active MCP Range-of-Motion Exercises, and active bidigital pinching movements in the transparent mode.
Intervention Type
Device
Intervention Name(s)
WRL HX MCP
Intervention Description
WRL HX MCP is a non CE marked class IIa medical device designed for clinical application in hand rehabilitation; it consists in a cable-driven robotic MCP orthosis providing flexion-extension of the metacarpo-phalangeal joint. WRL HX MCP features and a series-elastic actuators (SEA) architecture for compliant actuation of MCP flexion-extension and a self-aligning mechanism to absorb human/robot joint axes misplacement. Exoskeleton module is mounted on a dorsal hand support and connected to its electronic box through wires.
Primary Outcome Measure Information:
Title
Feasibility indicator: completion of study procedures
Description
Percent of participants for whom study procedures were completed successfully
Time Frame
through study completion, an average of 1 year
Title
Feasibility indicator: patient acceptability
Description
Clinician-generated questionnaire to investigate patients' impressions about the physical interaction with the robotic device
Time Frame
After the robotic therapy session; the total expected time for the session is about 90 minutes.
Title
Feasibility indicator: reliability evaluated through the number of device malfunctions
Description
The physiotherapist is required to report any malfunctions occurring during the study in regard to the use of WRL HX MCP
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Goniometric measure of MCP Active Range of Motion (AROM)
Description
The physiotherapist measures the MCP joint angles in maximum active flexion and extension using a short-arm goniometer
Time Frame
at baseline and immediately after the robotic therapy session.
Title
Goniometric measure of MCP Passive Range of Motion (PROM)
Description
The physiotherapist measures the MCP joint angles in maximum passive flexion and extension using a short-arm goniometer
Time Frame
at baseline and immediately after the robotic therapy session
Title
Robotic measure of MCP Active Range of Motion (AROM)
Description
MCP joint maximum active flexion and extension range of motion is registered while the device and human joint are coupled together, using WRL HX MCP set in a transparent mode as an evaluation tool, without any manual assistance.
Time Frame
at baseline and immediately after the robotic therapy session
Title
Robotic measure of MCP passive Range of Motion (PROM)
Description
MCP joint maximum passive flexion and extension range of motion is registered while the device and human joint are coupled together, using WRL HX MCP set in a transparent mode as an evaluation tool, with manual assistance from the therapist.
Time Frame
at baseline and immediately after the robotic therapy session
Title
Robotic estimation of MCP joint flexion peak torque
Description
MCP joint flexion peak torque is evaluated by the exoskeleton torque joint sensor during the robot-in-charge mobilization sequences
Time Frame
during robot-in-charge mobilization sequences
Title
Numeric Pain Rating Scale (NPRS)
Description
NPRS is an 11-point scale for patient self-reporting of pain, with 0 being "no pain" and 10 being "the worst pain imaginable"
Time Frame
at baseline and after each of the two series of joint mobilization exercises, lasting up to 30 minutes each.
Title
Safety evaluated through the number of adverse events
Description
The physiotherapist is required to report any adverse events occurring during the study in regard to the use of WRL HX MCP
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: history of traumatic hand injury or post-traumatic hand surgery hand size allowing to achieve proper exoskeleton fit NRS pain score in the 1-5 range Exclusion Criteria: cognitive or linguistic ability insufficient to understand instructions cardiac implanted electronic devices open skin at the level of the patient-device interface absence of contraindications for finger joints mobilisation current or prior history of malignancy pregnancy or breast feeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elisa Taglione, MD
Phone
+39058898456
Email
e.taglione@inail.it
First Name & Middle Initial & Last Name or Official Title & Degree
Ilaria Creatini, MD
Phone
+39058898422
Email
i.creatini@inail.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elisa Taglione, MD
Organizational Affiliation
INAIL - Centro di Riabilitazione Motoria di Volterra
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Simona Crea, PhD
Organizational Affiliation
The BioRobotics Institute, Scuola Superiore Sant'Anna
Official's Role
Study Director
Facility Information:
Facility Name
INAIL - Centro di Riabilitazione Motoria di Volterra
City
Volterra
State/Province
Pisa
ZIP/Postal Code
56048
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elisa Taglione, MD
Phone
+39058898456
Email
e.taglione@inail.it
First Name & Middle Initial & Last Name & Degree
Ilaria Creatini, MD
Phone
+39058898422
Email
i.creatini@inail.it
First Name & Middle Initial & Last Name & Degree
Elisa Taglione, MD
First Name & Middle Initial & Last Name & Degree
Ilaria Creatini, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Citation
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Citation
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Results Reference
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Hand Motor Rehabilitation Using a Wearable Robotic Device (WRL HX MCP)

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