MedPath

Augmented visual feedback in upper limb stroke rehabilitatio

Completed
Conditions
Stroke
Circulatory System
Stroke, 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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Arm function assessed by the Action Research Arm Test (ARAT) at baseline, six weeks and six months
Secondary Outcome Measures
NameTimeMethod
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
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