Feasibility of a functional hand orthosis (MyHand) to support hand function in stroke

Feasibility of a functional hand orthosis (MyHand) to support hand function in stroke - Feasibility MyHand orthosis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON46169

Enrollment

Registered

2016-06-17

Start date

2017-05-19

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

cerebrovascular accident Stroke

Interventions

All subjects will receive the same intervention: use of a dynamic functional hand orthosis to support hand function during functional tasks.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Time post-stroke at least 4 weeks - Hemiparesis of arm and hand (Brunnstrom stage 3-4) - Age between 18 and 80 - Able to complete sessions (at least 3,5h) - Free from co-morbidity that affects movement of the arm - Free from fixed contractures in arm and hand - Mentally competent and able to follow instructrions

Exclusion criteria

Exclusion criteria: - Potential other diseases that affect the wellbeing of the subject and the measurements (such as fever, flu, etc.)

Design outcomes

Primary

Measure	Time frame
Main outcome measure is the Wolf Motor Function Test (WMFT).	—

Secondary

Measure	Time frame
Action Research Arm Test (ARAT), System Usability Scale (SUS), Motor Activity Log (MAL), an interview (including Patiënt Specifieke Klachten (PSK) lijst) and a diary in which the use duration per activity will be noted.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)