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

Completed

• Conditions: cerebrovascular accident; Stroke; 10007963

• Registration Number: NL-OMON46169
• Lead Sponsor: Revalidatiecentrum Het Roessingh

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 5

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

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main outcome measure is the Wolf Motor Function Test (WMFT).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Action Research Arm Test (ARAT), System Usability Scale (SUS), Motor Activity<br /><br>Log (MAL), an interview (including *Patiënt Specifieke Klachten (PSK) lijst*)<br /><br>and a diary in which the use duration per activity will be noted.</p><br>