- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT03561155
Robot-assisted Arm Training in Multiple Sclerosis (RAMSES)
18. Juni 2018 aktualisiert von: 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.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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)
Studientyp
Interventionell
Einschreibung (Tatsächlich)
60
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Verona, Italien, 37134
- UOC Neurorehabilitation
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre bis 65 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Alle
Beschreibung
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
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 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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Aktiver Komparator: 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 |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Action Research Arm test
Zeitfenster: 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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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Fugl-Meyer Assessment Motor Scale - Arm Section
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Hauptermittler: Nicola Smania, Professor, Universita di Verona
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
1. November 2014
Primärer Abschluss (Tatsächlich)
1. September 2017
Studienabschluss (Tatsächlich)
1. Mai 2018
Studienanmeldedaten
Zuerst eingereicht
23. Mai 2018
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
18. Juni 2018
Zuerst gepostet (Tatsächlich)
19. Juni 2018
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
19. Juni 2018
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
18. Juni 2018
Zuletzt verifiziert
1. Juni 2018
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- FISM 14/14/F14
Plan für individuelle Teilnehmerdaten (IPD)
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