Robot-assisted Arm Training in Multiple Sclerosis (RAMSES)
Primary Purpose
Multiple Sclerosis, Rehabilitation
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Robot assisted treatment (Amadeo®)
Conventional treatment
Sponsored by

About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring Upper Extremity, Recovery
Eligibility Criteria
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
Sites / Locations
- UOC Neurorehabilitation
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Robot assisted treatment
Conventional treatment
Arm Description
The experimental group (EG) will undergo a robot-assisted arm training using Amadeo® (Tyromotion-Austria).
The conventional group (CG) will undergo robot unassisted treatment (Conventional treatment).
Outcomes
Primary Outcome Measures
Action Research Arm test
Assesses upper limb functioning using observational methods
Secondary Outcome Measures
Fugl-Meyer Assessment Motor Scale - Arm Section
Evaluates and measures recovery in post-stroke hemiplegic patients
Motor Activity Log
Semi-structured interview to assess arm function.
Tremor Severity Scale
A clinical rating scale which measured the severity of tremor
Nine Hole Peg Test
Measures finger dexterity
Motricity Index
Measures of strength in upper limb
Amadeo® hand muscle strength (Newton)
Measures of muscle strenght using the robotic device
Visual anolgue Scale for tiredness and fatigue
Measures of tirediness and fatigue on a 10-point likert scale
Multiple Sclerosis Quality of Life-54
Measures of a multidimensional health-related quality of life measure that combines both generic and MS-specific items into a single instrument.
Assessment of Life Habits
Assesses participants on 77 life habits from daily activities to social participation across 12 domains.
UL electromyographic analysis of muscle activation
Instrumental assessment of muscle activity during a reaching task
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03561155
Brief Title
Robot-assisted Arm Training in Multiple Sclerosis
Acronym
RAMSES
Official 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
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
November 2014 (Actual)
Primary Completion Date
September 1, 2017 (Actual)
Study Completion Date
May 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universita di Verona
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Rehabilitation
Keywords
Upper Extremity, Recovery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Robot assisted treatment
Arm Type
Experimental
Arm Description
The experimental group (EG) will undergo a robot-assisted arm training using Amadeo® (Tyromotion-Austria).
Arm Title
Conventional treatment
Arm Type
Active Comparator
Arm Description
The conventional group (CG) will undergo robot unassisted treatment (Conventional treatment).
Intervention Type
Device
Intervention Name(s)
Robot assisted treatment (Amadeo®)
Other Intervention Name(s)
Robot assisted treatment
Intervention Description
The protocol will consist of exercises as follows:
passive modality , passive/plus modality , assisted therapy and Balloon.
Intervention Type
Other
Intervention Name(s)
Conventional treatment
Intervention Description
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 Outcome Measure Information:
Title
Action Research Arm test
Description
Assesses upper limb functioning using observational methods
Time Frame
Up to 6 weeks
Secondary Outcome Measure Information:
Title
Fugl-Meyer Assessment Motor Scale - Arm Section
Description
Evaluates and measures recovery in post-stroke hemiplegic patients
Time Frame
Up to 6 weeks
Title
Motor Activity Log
Description
Semi-structured interview to assess arm function.
Time Frame
Up to 6 weeks
Title
Tremor Severity Scale
Description
A clinical rating scale which measured the severity of tremor
Time Frame
Up to 6 weeks
Title
Nine Hole Peg Test
Description
Measures finger dexterity
Time Frame
Up to 6 weeks
Title
Motricity Index
Description
Measures of strength in upper limb
Time Frame
Up to 6 weeks
Title
Amadeo® hand muscle strength (Newton)
Description
Measures of muscle strenght using the robotic device
Time Frame
Up to 6 weeks
Title
Visual anolgue Scale for tiredness and fatigue
Description
Measures of tirediness and fatigue on a 10-point likert scale
Time Frame
Up to 6 weeks
Title
Multiple Sclerosis Quality of Life-54
Description
Measures of a multidimensional health-related quality of life measure that combines both generic and MS-specific items into a single instrument.
Time Frame
Up to 6 weeks
Title
Assessment of Life Habits
Description
Assesses participants on 77 life habits from daily activities to social participation across 12 domains.
Time Frame
Up to 6 weeks
Title
UL electromyographic analysis of muscle activation
Description
Instrumental assessment of muscle activity during a reaching task
Time Frame
Up to 6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicola Smania, Professor
Organizational Affiliation
Universita di Verona
Official's Role
Principal Investigator
Facility Information:
Facility Name
UOC Neurorehabilitation
City
Verona
ZIP/Postal Code
37134
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30405526
Citation
Gandolfi M, Vale N, Dimitrova EK, Mazzoleni S, Battini E, Benedetti MD, Gajofatto A, Ferraro F, Castelli M, Camin M, Filippetti M, De Paoli C, Chemello E, Picelli A, Corradi J, Waldner A, Saltuari L, Smania N. Effects of High-intensity Robot-assisted Hand Training on Upper Limb Recovery and Muscle Activity in Individuals With Multiple Sclerosis: A Randomized, Controlled, Single-Blinded Trial. Front Neurol. 2018 Oct 24;9:905. doi: 10.3389/fneur.2018.00905. eCollection 2018.
Results Reference
derived
Learn more about this trial
Robot-assisted Arm Training in Multiple Sclerosis
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