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Completed

NCT Number: NCT03561155

Robot-assisted Arm Training in Multiple Sclerosis

The upper limb (UL) plays an important role in the daily functioning of patients with Multiple Sclerosis (MS) and negatively influences their quality of life. Effective arm-hand training programs are needed. Various robotic systems have been developed for UL rehabilitation, mainly used in patients with stroke. Preliminary work in MS has focused on proximal sections of the arm. No study has evaluated the use of robotics for improving manual dexterity and their effects on cortical activity. The results of this research project could be relevant for the advancement of knowledge about UL functional recovery in individuals with MS and to determine the pattern of muscle activation underlying functional recovery.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UOC Neurorehabilitation

Verona, 37134, Italy

About this study

Studies regarding the effectiveness of conventional and robot-based upper limb (UL) rehabilitation in individuals with MS is very limited.In the last 15 years, conventional rehabilitation of the UL in patients with neurological disorders has been enriched by the development of robots as they can provide high-intensity, repetitive, interactive and task-specific exercises.They are increasingly used in rehabilitation after stroke, therefore may also be good candidates for neuromotor rehabilitation of patients with MS. Furthermore, these devices can provide various feedbacks that can guide patients during the sensorimotor training and allow quantitative measurement of motor performance during training.One of these devices is the Amadeo®, a modern, mechatronic end-effector robotic device designed to improve sensorimotor functions in patients with restricted movement in individual fingers or in the entire hand.Another important issue concerns cortical plasticity, which plays a fundamental role in motor learning and neurorehabilitation.To date, the specific mechanisms leading to UL recovery after neurological rehabilitation are still unclear.The development of new EEG instruments allows brain activity to be tested under specific rehabilitation tasks contributes to give new insight in the dynamics of cortical networks reorganization promoted by rehabilitation.The main aim of the study is to perform a single blind RCT on 60 outpatients with MS (age:18-65 years;EDSS<8) in order to compare the efficacy of high-intensity robot-assisted training with conventional treatment on sensorimotor hand recovery, disability in ADLs and QoL.The secondary aim is to explore the underlying neuronal mechanisms of UL recovery by using EEG investigations and innovative robotic equipment. 10 controls (age 18-65 yrs) will undergo one session of the same Video-EEG acquisition to collect normative data to compare with data collected on patients.Each participant will receive 40-minute sessions over an 8 week period (3 days/week). Each session will consist of 30 minutes of hand training and 10 minutes of passive upper limbs mobilization.The experimental group will receive robot-assisted therapy by Amadeo.The control group will receive conventional rehabilitation.Before treatment, immediately after treatment, 1 month after treatment patients will be evaluated with a comprehensive protocol of all ICF domains as well as acquisition by Video-EEG acquisition combined with Amadeo® robotic training device.Primary outcome measures:Fugl-Meyer Assessment Motor Scale.Secondary measures: UL electromyographic analysis,Tremor Severity Scale, Nine Hole Peg Test, Amadeo® hand muscle strength (Newton), Motricity Index, Visual anolgue Scale for tiredness and fatigue; TEMPA, Motor Activity Log, Action Research Arm test, Multiple Sclerosis Quality of Life-54 and the assessment of Life Habits. Parametric tests and nonparametric tests will be performed according to variable distribution (p<.05)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 18-65 years
  • EDSS score<8
  • Mini Mental State Evaluation (MMSE) score>24
  • Ashworth Scale Score<2 evaluated at the elbow, wrist and fingers
  • Nine Hole Peg Test (NHPT) score >30 sec.

Exclusion criteria

  • Disease recurrence that worsened significantly during the 3 months prior to recruitment
  • Medical therapy not well defined
  • Musculoskeletal impairments or excessive pain in any joint that could limit participation in an exercise program
  • Severe visual dysfunction
  • Performance of any type of rehabilitation treatment in the month prior to recruitment
  • Other concomitant neurological or orthopaedic diseases involving the UL and interfering with their function

Treatment and study plan

Robot assisted treatment (Amadeo®)

Device

The protocol will consist of exercises as follows:

passive modality , passive/plus modality , assisted therapy and Balloon.

Other names: Robot assisted treatment

conventional treatment

Other

The protocol will consist of exercises as follow:

upper limb mobilization, facilitation of movements and active tasks. The exercises will be focused on improving muscle strength, finger extension and flexion and motor control

Primary outcomes

  1. Action Research Arm test

    Time frame: Up to 6 weeks

    Assesses upper limb functioning using observational methods

Secondary outcomes

  1. Fugl-Meyer Assessment Motor Scale - Arm Section

    Time frame: Up to 6 weeks

    Evaluates and measures recovery in post-stroke hemiplegic patients

  2. Motor Activity Log

    Time frame: Up to 6 weeks

    Semi-structured interview to assess arm function.

  3. Tremor Severity Scale

    Time frame: Up to 6 weeks

    A clinical rating scale which measured the severity of tremor

  4. Nine Hole Peg Test

    Time frame: Up to 6 weeks

    Measures finger dexterity

  5. Motricity Index

    Time frame: Up to 6 weeks

    Measures of strength in upper limb

  6. Amadeo® hand muscle strength (Newton)

    Time frame: Up to 6 weeks

    Measures of muscle strenght using the robotic device

  7. Visual anolgue Scale for tiredness and fatigue

    Time frame: Up to 6 weeks

    Measures of tirediness and fatigue on a 10-point likert scale

  8. Multiple Sclerosis Quality of Life-54

    Time frame: Up to 6 weeks

    Measures of a multidimensional health-related quality of life measure that combines both generic and MS-specific items into a single instrument.

  9. Assessment of Life Habits

    Time frame: Up to 6 weeks

    Assesses participants on 77 life habits from daily activities to social participation across 12 domains.

  10. UL electromyographic analysis of muscle activation

    Time frame: Up to 6 weeks

    Instrumental assessment of muscle activity during a reaching task

Sponsors and collaborators

Lead sponsor

Universita di Verona

Other

Registry information

Official study title

Effects of High-intensity Robot-assisted Training in Hand Function Recovery and ADL Independence in Individuals With Multiple Sclerosis: a Randomized Controlled Single-blinded Trial

Acronym: RAMSES

Important dates

Study start
2014
Primary completion
2017
Study completion
2018
First posted
Jun 19, 2018
Registry last updated
Jun 19, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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