Sensor-based Technology for Upper Limb Rehabilitation

Sponsor
I.R.C.C.S. Fondazione Santa Lucia (Other)
Overall Status
Completed
CT.gov ID
NCT04367285
Collaborator
(none)
35
1
2
35
1

Study Details

Study Description

Brief Summary

Sensor-based technological therapy devices may be good candidates for neuromotor rehabilitation of people with Multiple Sclerosis (MS), especially for treating upper extremities function limitations. The sensor-based device rehabilitation is characterized by interactive therapy games with audio-visual feedback that allows training the movement of shoulders, elbows and wrist, measuring the strength and the active range of motion of upper limb, registering data in an electronic database in order to quantitatively monitoring measures and therapy progress. The aim of this study is to evaluate the effects of sensor-based motor rehabilitation in add-on to the conventional neurorehabilitation, on increasing the upper limbs functions of MS patients. The training consisting of twelve sessions of upper limb training, was compared with twelve sessions of upper limb sensory-motor training, without robotic support. Both rehabilitation programs were performed for 40 minutes three times a week, for 4 weeks, in addition to the conventional therapy. All patients were evaluated at baseline (T0) and after 4 weeks of training (T1)

Condition or Disease Intervention/Treatment Phase
  • Other: Sensor-based Training
  • Other: Upper limb motor training
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
35 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Sensor-based Technology for Upper Limb Rehabilitation in Subject With Multiple Sclerosis: a Randomized Controlled Trial
Actual Study Start Date :
Mar 1, 2017
Actual Primary Completion Date :
Nov 4, 2019
Actual Study Completion Date :
Jan 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sensor-based Training

Other: Sensor-based Training
Sensor-based Training consists of twelve sessions of upper limb training with PABLO®-Tyromotion. For each session the training consists in interactive-games based on virtual reality which allowed a task-oriented approach and a neurocognitive feedback. The exercises require precision tasks and one-dimensional and bidimensional reaction, allowing to train the attention, the strength control and movement control, the coordination and the movement precision. The interactive-games were chosen from those proposed by the Tyromotion PABLO® System.

Active Comparator: Upper limb motor training

Other: Upper limb motor training
Upper limb motor training, without robotic support. Subjects performed specific exercises aimed to recovery global upper limb functions, to control hand grasp and to improve hand's fine movements.

Outcome Measures

Primary Outcome Measures

  1. Changes in functionality of the upper limb measured in 9 Hole Peg Test (9HPT) at 1 months [1 month]

    Changes in functionality of the upper limb measured in 9-HPT. Changes in the measure in 9-HPT (time, seconds *total scale*) Nine Hole PegTest (Mathiowetz et al, Occup Therap J Resaerach 1985) Time in second to perform the whole test will be recordered (better with less time)

Secondary Outcome Measures

  1. Fatigue Level at 1 month [1 month]

    Fatigue Severity Scale (FSS) is one of the most commonly used self-report questionnaires to measure fatigue. Each question on this scale, which is composed of Likert type questions: 1.I strongly disagree 2.I do not agree 3.No tend to disagree 4. Indefinitely. The total score of the scale, which consists of 9 questions, varies between 9-63. People are asked to mark the appropriate options for each question taking into account their status in the last 1 month period. A total of 36 points and above indicate fatigue

  2. Modified Barthel Index (MBI) at 1 month [1 month]

    Change of Modified Barthel Index (MBI) at 1 month. MBI MBI values ranging from 0 to 105, where 0 means the worse outcome and 105 the best one.

  3. Changes in Multiple Sclerosis Quality of Life-54 questionnaire (MSQOL-54)at 1 month [1 month]

    Change from Baseline in MSQOL-54. MSQOL-54 is a multidimensional health-related quality of life measure, assessing the perception of physical and mental well-being. The instrument is composed of 54 items concerning 12 subscales, which form two scales relating to the physical and mental well-being. The score of the physical function scales, perceptions of health, energy/fatigue, role-physical limitations, pain, sexual function, social function, health distress, is added and corrected to obtain a score on the MSQUOL PHYSICAL HEALTH scale: a score above 50.0 indicates physical well-being. The score of the health distress scale, overall quality of life, emotional well-being, role limitations - emotional, cognitive function is summed and corrected to obtain a score on the scale MSQUOL MENTAL HEALTH: a score above 50.0 indicates mental well-being. The administration time is about 11-18 minutes, it can be completed by an interviewer or by the patient.

  4. Changes of Medical Research Council scale (MRC) at 1 month [1 month]

    The MRC score is obtained by evaluating 12 muscle groups in the upper extremities (wrist extensors, elbow flexors and abductors of the shoulder) and lower extremities (dorsal ankle flexors, knee extensors, and hip flexors). For each muscle group will be assigned a score between 0 (complete paralysis) and 5 (normal force), and the total score can vary between 0 up to 60 points.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • diagnosis of Multiple Sclerosis

  • upper limb deficits,

  • disability between 5 and 8.5 on the Expanded Disability Status Scale (EDSS).

Exclusion Criteria:
  • Modified Ashworth Scale (MAS) < 3 at the upper limb;

  • cognitive deficits affecting the ability to understand task instructions (Mini-Mental State Examination < 24

  • Medical Research Council (MRC) scale with score 0 or 5;

  • presence of clinically evaluated severe comorbidities; pregnancy;

  • subjects with artificial pacemaker;

  • subjects involved in other studies.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marco Tramontano Rome Italy 00179

Sponsors and Collaborators

  • I.R.C.C.S. Fondazione Santa Lucia

Investigators

  • Principal Investigator: Marco Tramontano, SANTA LUCIA FOUNDATION

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marco Tramontano, head of rehabilitation Services, I.R.C.C.S. Fondazione Santa Lucia
ClinicalTrials.gov Identifier:
NCT04367285
Other Study ID Numbers:
  • FSLCE/PROG.631
First Posted:
Apr 29, 2020
Last Update Posted:
Apr 29, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 29, 2020