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Invloed van een robotische handschoen op het reiken en grijpen na CVA

Conditions
pper extremity impairment after strokeCVAFuntiebeperking bovenste extremiteit na een beroerte
Registration Number
NL-OMON20620
Lead Sponsor
Roessingh Research and Development BV, Enschede
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

Patients should be clinically diagnosed with unilateral ischemic or hemorrhagic stroke

- Between 18-80 years of age

Exclusion Criteria

- People with severe sensory problems of the affected upper extremity

- People with severe acute pain of the affected arm -People who participate in other studies that can affect functional performance of the arm and hand

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The main study parameters are outcomes related to (functional) task performance and movement execution. To examine the direct influence of the grasp support system on (functional) performance of the most-affected arm and hand during the different proposed conditions, the following main study parameters will be measured: • Qualitative observations of functional task performance and movement execution (e.g. speed of movement, precision, fluidity, compensatory movements) • Quantitative parameters of functional task performance and movement execution (e.g. performance time, kinematics of hand and arm joints, movement path, velocity (profile), acceleration and jerk)
Secondary Outcome Measures
NameTimeMethod
To explore user acceptance of the grasp support system and to examine the direct effect of the grasp support system on changes in hand strength and movement execution, the following parameters will be registered during the measurements: • System Usability Scale (SUS) • Semi-structured interview about user’s experience • Action Research Arm Test (ARAT) • Maximal pinch force (Jamar pinch Gauge dynamometer)
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