MedPath

hoMEcare aRm rehabiLItatio

Completed
Conditions
Stroke (single) with resulting unilateral paresis.
Registration Number
NL-OMON28842
Lead Sponsor
MCG
Brief Summary

Rozevink, S. G., Sluis, C. K. van der, Garzo, A., Keller, T., & Hijmans, J. M. (2021). hoMEcare aRm rehabiLItatioN (MERLIN): Telerehabilitation using an unactuated device based on serious games improves the upper limb function in chronic stroke. Journal of NeuroEngineering and Rehabilitation (InPress), 18(48), 1–12. https://doi.org/10.1186/s12984-021-00841-3 Rozevink, S. G., van der Sluis, C. K., & Hijmans, J. M. (2021). HoMEcare aRm rehabiLItatioN (MERLIN): preliminary evidence of long term effects of telerehabilitation using an unactuated training device on upper limb function after stroke. Journal of NeuroEngineering and Rehabilitation, 18(141), 1–9. https://doi.org/https://doi.org/10.1186/s12984-021-00934-z

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
15
Inclusion Criteria

18 years or older
-Unilateral paresis with at least some proximal voluntary movement capability (max FMA-UE = 50)
-First incidence of single stroke or stuttering stroke
-Minimal 6 months and maximal 3 years post-stroke
-Able to perform finger extension 3 times
-Ability to give informed consent, understand and execute simple instructions
-Visual, mental and cognitive ability to assimilate and actively participate in the protocol
-Being able to speak and understand Dutch/English
-Know how to operate a computer (or have someone to help) and have the possibility to train at home.

Exclusion Criteria

-Multiple strokes or bilateral impairment
-Inability to give informed consent
-Moderate or severe cognitive impairment
-Depression
-Other medical disorders which could have effect on the results of the intervention such as rheumatic disorders or shoulder pain
-Following occupational or physiotherapy specifically focussed on the arm/hand
-Patients who have a positive predictor within 24 hours, such as wrist movement

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Wolf Motor Function Test (WMFT)
Secondary Outcome Measures
NameTimeMethod
Action Research Arm Test (ARAT), Fugl-Meyer Assessment-Upper Extremity (FMA-UE), EuroQol-5D (EQ-5D), Intrinsic Motivation Inventory (IMI), System Usability Scale (SUS), Dutch Quebec User Evaluation of Satisfaction with Assistive Technology (D-QUEST) and biomechanical data using the ArmAssist Assessment (AAA) and Inertial Measurement Units (IMUs). Subjective opinion of the patient about the effectiveness and usability will be assessed during in-depth interviews.
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