NL-OMON50142尚未招募不适用
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.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- 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
- •five weeks from the start of the study.
排除标准
- •- 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
- •messages from the display of the hand activity tracker.
- •- Potential non-compliance, such as known intolerance to the device material,
- •major comorbidities (e.g. cardiopulmonary disease, orthopaedic disorders of the
- •upper limb).
- •- Major depression.
研究者
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