Robot-assisted Arm Training in Multiple Sclerosis (RAMSES)
2018年6月18日 更新者: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.
調査の概要
詳細な説明
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)
研究の種類
介入
入学 (実際)
60
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Verona、イタリア、37134
- UOC Neurorehabilitation
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年~65年 (大人、高齢者)
健康ボランティアの受け入れ
はい
受講資格のある性別
全て
説明
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
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:単一グループの割り当て
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的: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.
他の名前:
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アクティブコンパレータ: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 |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Action Research Arm test
時間枠: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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Fugl-Meyer Assessment Motor Scale - Arm Section
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者:Nicola Smania, Professor、Universita di Verona
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2014年11月1日
一次修了 (実際)
2017年9月1日
研究の完了 (実際)
2018年5月1日
試験登録日
最初に提出
2018年5月23日
QC基準を満たした最初の提出物
2018年6月18日
最初の投稿 (実際)
2018年6月19日
学習記録の更新
投稿された最後の更新 (実際)
2018年6月19日
QC基準を満たした最後の更新が送信されました
2018年6月18日
最終確認日
2018年6月1日
詳しくは
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