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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38106
Enrollment
87
Registered
2011-04-07
Start date
2011-05-02
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stroke-related arm-hand function and skill performance problems arm-hand skill performance problems stroke

Interventions

None listed

Sponsors

Adelante Kenniscentrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

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

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)