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CompletedNCT04367285Updated Apr 29, 2020

Sensor-based Technology for Upper Limb Rehabilitation

An interventional study of Sensor-based Training and Upper limb motor training in Multiple Sclerosis, sponsored by I.R.C.C.S. Fondazione Santa Lucia. Completed at 1 site in Italy. Open to participants aged 30 Years to 70 Years. Per ClinicalTrials.gov, last updated 2020-04-29.

Sponsored by I.R.C.C.S. Fondazione Santa Lucia · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 1 month after the study started (first participant enrolled Mar 2017, registered Apr 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Randomized
Ages
30 Years to 70 Years
Sex
All
01

Study 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)

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Conditions studied

  • Multiple Sclerosis
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In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's enrollment of 35 is below the median of 50 across 2,342 interventional studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

I.R.C.C.S. Fondazione Santa Lucia is the lead sponsor of 56 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
30 Years to 70 Years
Sexes eligible
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

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.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Sensor-based Training

    Other: Sensor-based Training

  • Active comparator
    Upper limb motor training

    Other: Upper limb motor training

Interventions

  • OtherSensor-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.

  • OtherUpper 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.

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What researchers measure

Primary outcomes

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

    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)

    Time frame: 1 month

Secondary outcomes

  1. Fatigue Level at 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

    Time frame: 1 month

  2. Modified Barthel Index (MBI) at 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.

    Time frame: 1 month

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

    Time frame: 1 month

  4. Changes of Medical Research Council scale (MRC) at 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.

    Time frame: 1 month

07

Study locations

1 site
  • Marco Tramontano
    Rome, 00179, Italy
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04367285
Lead sponsor
I.R.C.C.S. Fondazione Santa Lucia
Responsible party
Marco Tramontano (head of rehabilitation Services, I.R.C.C.S. Fondazione Santa Lucia) — Principal investigator
First posted
Apr 29, 2020
Start date
Mar 1, 2017
Primary completion
Nov 4, 2019
Completion
Jan 31, 2020
Last update
Apr 29, 2020

Study contacts

Marco Tramontano
principal investigator · SANTA LUCIA FOUNDATION

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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