Evaluation of a Robotic Device for Rapid Assessment of Hand Sensorimotor Functio

• Conditions: I64; Stroke, not specified as haemorrhage or infarction

• Registration Number: DRKS00018681
• Lead Sponsor: Kliniken Schmieder Allensbach

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-09-26
• Study Completion: 2020-03-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

Diagnosis of stroke (ischemic or hemorrhagic)

Exclusion Criteria

Complete paralysis, pain when placing the hand in the device, inability to understand task instructions , minimum passive range of motion of MCP joint smaller than 20 degrees, maximum 40% of subjects (12/30) with unimpaired proprioception (Kinesthetic Up-Down Test KUDT in Nottingham Sensory Assessment 3/3), maximum 40% of subjects (12/30) with severely impaired proprioception (KUDT: 0/3), severe spasticity for finger flexors (Modified Ashworth Scale > 2)

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Robotic outcome measures (i.e. index finger velocity, position, force)

Secondary Outcome Measures

Name	Time	Method
Clinical outcomes: Box & Block test, Nottingham Sensory Assessment, Montreal Cognitive Assessment, Fugl-Meyer Assessment