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Robot-assisted Arm Training in Multiple Sclerosis (RAMSES)
18 juni 2018 bijgewerkt door: Nicola Smania, MD, Clinical Professor, Universita di Verona
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
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.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
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)
Studietype
Ingrijpend
Inschrijving (Werkelijk)
60
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Verona, Italië, 37134
- UOC Neurorehabilitation
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 65 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
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
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Robot assisted treatment
The experimental group (EG) will undergo a robot-assisted arm training using Amadeo® (Tyromotion-Austria).
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The protocol will consist of exercises as follows: passive modality , passive/plus modality , assisted therapy and Balloon.
Andere namen:
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Actieve vergelijker: Conventional treatment
The conventional group (CG) will undergo robot unassisted treatment (Conventional treatment).
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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 |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Action Research Arm test
Tijdsspanne: Up to 6 weeks
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Assesses upper limb functioning using observational methods
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Up to 6 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Fugl-Meyer Assessment Motor Scale - Arm Section
Tijdsspanne: Up to 6 weeks
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Evaluates and measures recovery in post-stroke hemiplegic patients
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Up to 6 weeks
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Motor Activity Log
Tijdsspanne: Up to 6 weeks
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Semi-structured interview to assess arm function.
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Up to 6 weeks
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Tremor Severity Scale
Tijdsspanne: Up to 6 weeks
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A clinical rating scale which measured the severity of tremor
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Up to 6 weeks
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Nine Hole Peg Test
Tijdsspanne: Up to 6 weeks
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Measures finger dexterity
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Up to 6 weeks
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Motricity Index
Tijdsspanne: Up to 6 weeks
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Measures of strength in upper limb
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Up to 6 weeks
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Amadeo® hand muscle strength (Newton)
Tijdsspanne: Up to 6 weeks
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Measures of muscle strenght using the robotic device
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Up to 6 weeks
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Visual anolgue Scale for tiredness and fatigue
Tijdsspanne: Up to 6 weeks
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Measures of tirediness and fatigue on a 10-point likert scale
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Up to 6 weeks
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Multiple Sclerosis Quality of Life-54
Tijdsspanne: Up to 6 weeks
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Measures of a multidimensional health-related quality of life measure that combines both generic and MS-specific items into a single instrument.
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Up to 6 weeks
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Assessment of Life Habits
Tijdsspanne: Up to 6 weeks
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Assesses participants on 77 life habits from daily activities to social participation across 12 domains.
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Up to 6 weeks
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UL electromyographic analysis of muscle activation
Tijdsspanne: Up to 6 weeks
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Instrumental assessment of muscle activity during a reaching task
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Up to 6 weeks
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Nicola Smania, Professor, Universita di Verona
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 november 2014
Primaire voltooiing (Werkelijk)
1 september 2017
Studie voltooiing (Werkelijk)
1 mei 2018
Studieregistratiedata
Eerst ingediend
23 mei 2018
Eerst ingediend dat voldeed aan de QC-criteria
18 juni 2018
Eerst geplaatst (Werkelijk)
19 juni 2018
Updates van studierecords
Laatste update geplaatst (Werkelijk)
19 juni 2018
Laatste update ingediend die voldeed aan QC-criteria
18 juni 2018
Laatst geverifieerd
1 juni 2018
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- FISM 14/14/F14
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
ONBESLIST
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