AMUSE: Activity Monitoring of Upper extremity use in Stroke patients during and after rEhabilitation: a new step towards a solution of an old problem

Recruiting

• Conditions: stroke-related arm-hand function and skill performance problems; arm-hand skill performance problems; stroke; 10007963

• Registration Number: NL-OMON38106
• Lead Sponsor: Adelante Kenniscentrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 87

Inclusion Criteria

- age >=18 years,
- clinically diagnosed with central paresis of the arm/hand at entry in the study,
- a fair cognitive level, i.e. being able to understand the questionnaires and measurement instructions.

Exclusion Criteria

- additional complaints that may interfere with the execution of the measurements,
- no informed consent.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>- Amount of arm-hand use on both affected and non-affected side: accelerometry<br /><br>- Function level measures: Fugl-Meyer Motor Assessment (FM), and JAMAR<br /><br>- Activity level measures: Action Research Arm Test (ARAT), ABILHAND, and<br /><br>Stroke Impact Scale (SIS)<br /><br>- Quality of life measure: EuroQol-6D </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-</p><br>