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Experimentation of Sensorized Pseudoelastic Orthoses Produced by Additive Manufacturing

Primary Purpose

Acquired Brain Injury

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
pseudoelastic orthosis
Sponsored by
IRCCS Eugenio Medea
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acquired Brain Injury

Eligibility Criteria

6 Years - 20 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Quadriplegia or acquired hemiplegia.
  2. Age 6-20 years.
  3. Dystonic, dyskinetic, spastic.
  4. Chronic phase patients (> 1 year post event).
  5. Spastic syndrome with Ashworth Score (AS) for the limb of interest> 1.
  6. Collaborative.

Exclusion Criteria:

  1. Fixed limitations of the joint.
  2. Joint pain.
  3. Skin allergies.
  4. Behavioral and psychiatric disorders (eg, emotional problems, anxiety, panic attacks).

Sites / Locations

  • IRCCS Eugenio MedeaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Treatment

Control

Arm Description

Upper limb rehabilitation with pseudoelastic orthosis

Upper limb rehabilitation without pseudoelastic orthosis

Outcomes

Primary Outcome Measures

Joint Stiffness of affected upper limb joint
Quantitative measure performed by means of an isokinetic machine (Unit of measure: Nm/°). Changes in joint stiffness following the use of new customized devices during a rehabilitation treatment period. Lower stiffness is better.

Secondary Outcome Measures

Modified Ashworth Scale
Clinical scale for spasticity (5 levels), higher is worse.
Melbourne Upper Limb Assessment 2
Clinical scale for evaluating quality of upper limb movement (16 items, each assessed from 0 to 4 points). Result reported in %. Higher is better.
Quality of Upper Extremity Skills Test
Clinical scale evaluating the quality of upper extremity function (33 items, 4 domains). Minimum score 0, maximum score 100. Higher is better.
Active range of motion
Measured with goniometer in degrees.
Passive range of motion
Measured with goniometer in degrees.
Range of motion of target joint during a pointing-forward task
Measured in degrees. A kinematic analysis will be performed during a pointing-forward task using an optoelectronic system.

Full Information

First Posted
February 27, 2020
Last Updated
February 6, 2023
Sponsor
IRCCS Eugenio Medea
Collaborators
CNR - ICMATE UOS di Lecco
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1. Study Identification

Unique Protocol Identification Number
NCT04328857
Brief Title
Experimentation of Sensorized Pseudoelastic Orthoses Produced by Additive Manufacturing
Official Title
Experimentation of Sensorized Pseudoelastic Orthoses Produced by Additive Manufacturing
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
May 31, 2023 (Anticipated)
Study Completion Date
May 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IRCCS Eugenio Medea
Collaborators
CNR - ICMATE UOS di Lecco

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The proposed clinical investigation plan is a pivotal controlled study with two parallel groups, has a total duration of 12 months and involves the recruitment of 34 pediatric patients suffering from acquired brain injury. The primary objective of the clinical study is to evaluate the improvement of joint stiffness through the use of sensorized pseudoelastic orthoses for the rehabilitation of pediatric patients with acquired brain injury. The effectiveness of the treatment in terms of joint stiffness (primary outcome) will be assessed and the effect of the treatment will be quantified with clinical evaluation scales and instrumental measurements by means of an optoelectronic system and isokinetic machine. The tolerability and acceptability of the device will also be checked.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acquired Brain Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
Upper limb rehabilitation with pseudoelastic orthosis
Arm Title
Control
Arm Type
No Intervention
Arm Description
Upper limb rehabilitation without pseudoelastic orthosis
Intervention Type
Device
Intervention Name(s)
pseudoelastic orthosis
Intervention Description
The subject will be given specific physiotherapy including activities oriented to multimodal exploration and refinement of gross and fine motor skills, customized according to the functional status of the individual patient.
Primary Outcome Measure Information:
Title
Joint Stiffness of affected upper limb joint
Description
Quantitative measure performed by means of an isokinetic machine (Unit of measure: Nm/°). Changes in joint stiffness following the use of new customized devices during a rehabilitation treatment period. Lower stiffness is better.
Time Frame
After 4 weeks of treatment
Secondary Outcome Measure Information:
Title
Modified Ashworth Scale
Description
Clinical scale for spasticity (5 levels), higher is worse.
Time Frame
After 4 weeks of treatment
Title
Melbourne Upper Limb Assessment 2
Description
Clinical scale for evaluating quality of upper limb movement (16 items, each assessed from 0 to 4 points). Result reported in %. Higher is better.
Time Frame
After 4 weeks of treatment
Title
Quality of Upper Extremity Skills Test
Description
Clinical scale evaluating the quality of upper extremity function (33 items, 4 domains). Minimum score 0, maximum score 100. Higher is better.
Time Frame
After 4 weeks of treatment
Title
Active range of motion
Description
Measured with goniometer in degrees.
Time Frame
After 4 weeks of treatment
Title
Passive range of motion
Description
Measured with goniometer in degrees.
Time Frame
After 4 weeks of treatment
Title
Range of motion of target joint during a pointing-forward task
Description
Measured in degrees. A kinematic analysis will be performed during a pointing-forward task using an optoelectronic system.
Time Frame
After 4 weeks of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Quadriplegia or acquired hemiplegia. Age 6-20 years. Dystonic, dyskinetic, spastic. Chronic phase patients (> 1 year post event). Spastic syndrome with Ashworth Score (AS) for the limb of interest> 1. Collaborative. Exclusion Criteria: Fixed limitations of the joint. Joint pain. Skin allergies. Behavioral and psychiatric disorders (eg, emotional problems, anxiety, panic attacks).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elena Beretta
Phone
031877851
Email
elena.beretta@lanostrafamiglia.it
First Name & Middle Initial & Last Name or Official Title & Degree
FAbio A Storm
Email
fabio.storm@lanostrafamiglia.it
Facility Information:
Facility Name
IRCCS Eugenio Medea
City
Bosisio Parini
State/Province
LC
ZIP/Postal Code
23842
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elena Beretta, MD
Phone
+39031877111
Email
elena.beretta@lanostrafamiglia.it
First Name & Middle Initial & Last Name & Degree
Fabio A Storm

12. IPD Sharing Statement

Plan to Share IPD
No

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Experimentation of Sensorized Pseudoelastic Orthoses Produced by Additive Manufacturing

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