Augmented visual feedback in upper limb stroke rehabilitatio
- Conditions
- StrokeCirculatory SystemStroke, not specified as haemorrhage or infarction
- Registration Number
- ISRCTN14268457
- Lead Sponsor
- niversity of Strathclyde (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 45
1. Aged more than or equal to 18 years
2. Clinical diagnosis of stroke
3. Sub-acute stage of stroke (up to three months from time of onset of stroke)
4. Some movement in affected arm and/or hand - Action Research Arm Test (ARAT) score of 4-56 (57 max score)
5. Medically stable hence suitable for physical rehabilitation
6. Ability to understand and follow simple instructions
7. Able to give informed consent when assisted to do so with suitable communication aids
1. Pre-existing upper limb deficits
2. Bilateral arm impairments
3. Severe visual or cognitive problems precluding participation in study protocol
4. Involved in any other intervention study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Arm function assessed by the Action Research Arm Test (ARAT) at baseline, six weeks and six months
- Secondary Outcome Measures
Name Time Method 1. Kinematic (temporal and spatial parameters) assessment measured using sensors worn during a section of the ARAT<br>2. Hand function measured by the 9 Hole Peg Test<br>3. Stroke Impact Scale - to evaluate quality of life and disability changes<br>Measured at baseline, six weeks and six months<br><br>Additional outcome measures:<br>1. A patient and therapist questionnaire at 6 weeks to assess the acceptance of the visualisation system from their perspective<br>2. The safety of intervention assessed by number and nature of adverse events at end of intervention period and at follow up<br>3. Acceptance of the visualisation system will be assessed by withdrawal or dropout rates from study