Name (Synonyms) | Correlation |
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There is one clinical trial.
The COVID-19 outbreak requires a rapid re-shaping of the entire organization of the rehabilitation services. This includes the design and planning of appropriate rehabilitation settings, intervention and logistics for organizing space for patients. The aims of this study are: (a) to evaluate the feasibility of the bedside use of a novel rehabilitation device for upper limb in patients with stroke; (b) to evaluate the motor and cognitive outcomes of the treatment; (c) to validate the instrumental outcomes provided by the device.
Description: It is a tool for measuring the usability
Measure: System Usability Scale (SUS) Time: After 30 rehabilitation sessionsDescription: It is a tool for measuring the acceptability.
Measure: Technology Acceptance Model (TAM) Time: After 30 rehabilitation sessionsDescription: It is a tool for measuring the satisfaction.
Measure: Likert Scale Time: After 30 rehabilitation sessionsDescription: The Fugl-Meyer Assessment is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, sensation and joint functioning in patients with post-stroke hemiplegia. It is applied clinically and in research to determine disease severity, describe motor recovery, and to plan and assess treatment.
Measure: Fugl-Meyer Assessment for upper extremity (FMA-UE) Time: At baseline; after 30 rehabilitation sessionsDescription: It is a clinical instrument for characterizing the strength of the paretic upper extremity following stroke.
Measure: Motricity Index for the upper extremity (MI-UE) Time: At baseline; after 30 rehabilitation sessionsDescription: It is a clinical instrument for characterizing upper limb spasticity. Shoulder, elbow and wrist spasticity will be assessed.
Measure: Modified Ashworth Scale (MAS) Time: At baseline; after 30 session rehabilitation sessionsDescription: It is a unidimensional measure of pain intensity in adults.
Measure: Numeric Pain Rating Scale (NPRS) Time: At baseline; after 30 rehabilitation sessionsDescription: It is a measure of independence in activities of daily living.
Measure: Modified Barthel Index (mBI) Time: At baseline; after 30 rehabilitation sessionsDescription: It is a widely used screening assessment for detecting cognitive impairment.
Measure: Montreal Cognitive Assessment (MoCA) Time: At baseline; after 30 rehabilitation sessionsDescription: The kinematics of the end-effector of the robot will be acquired during point-to-point tasks.
Measure: Kinematic parameters Time: At baseline (twice, one day apart); after 10 rehabilitation sessions; after 20 rehabilitation sessions; after 30 rehabilitation sessions