NL-OMON50142
Not Yet Recruiting
N/A
A pilot study to investigate the feasibility of an intervention based on the Arm Activity Tracker in stroke patients. - Feasibility of the Arm Activity Tracker.
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Erasmus MC, Universitair Medisch Centrum Rotterdam
- Enrollment
- 20
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- People that suffered from an ischemic or hemorrhagic unilateral stroke more
- •than one week ago and less than six months ago.
- •\- The stroke resulted in new reduced upper limb function on one side.
- •\- Age: 18 years or older.
- •\- Inpatient in rehabilitation institute.
- •\- Subjects have to be able to lift the paretic arm against gravity.
- •\- Participants have to be able to do on/off the devices on both wrists
- •independently or with the assistance of a caregiver.
- •\- Participants need to be able to provide informed consent as documented by
- •\- The patient is planned to stay in the rehabilitation institute for at least
Exclusion Criteria
- •\- Severely reduced upper limb function which results in inability to lift the
- •affected hand off the lap when sitting.
- •\- Upper limb complications (e.g. frozen shoulder, severe upper limb pain).
- •\- Participants cannot comply with the study as a result of significant
- •cognitive, communication or visual impairment.
- •\- Severely impaired sensation resulting in inability to sense vibro\-tactile
- •triggers from the arm activity tracker.
- •\- Severely impaired vision which results in inability to read messages from the
- •display of the hand activity tracker.
- •\- Comprehensive aphasia which results in inability to read and/or understand
Outcomes
Primary Outcomes
Not specified
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