The SWIFT Cast Trial Protocol: A Randomized Controlled Evaluation of the Efficacy of an Ankle–Foot Cast on Walking Recovery Early after Stroke and the Neural–Biomechanical Correlates of Response

Author:

Pomeroy Valerie M.1,Rowe Phillip2,Baron Jean-Claude3,Clark Allan1,Sealy Richard4,Ugbolue Ukadike C.2,Kerr Ander2,

Affiliation:

1. Faculty of Medicine and Health Sciences, University of East Anglia, Norwich, UK

2. Bioengineering Department, University of Strathclyde, Glasgow, UK

3. Department of Clinical Neurosciences, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK

4. St George's NHS Trust, The Wolfson Centre, Wimbledon, London, UK

Abstract

Rationale An ankle–foot cast may enable people to repeatedly practice walking with a more normal movement pattern early after stroke. Aims To evaluate the clinical efficacy of using an ankle–foot cast [soft scotch ankle-foot (SWIFT) Cast] to enhance walking recovery and to find whether site of stroke lesion and/or baseline biomechanical characteristics predict response to a SWIFT Cast. Design Randomized, controlled, observer-blind trial. Study Participants ( n = 120), 3–42 days after stroke with walking difficulty. All will receive conventional physical therapy. Those allocated to the experimental group will also receive a SWIFT Cast for up to six-weeks. During therapy sessions, the SWIFT Cast will be worn for retraining of walking as clinically appropriate. Outside therapy sessions, participants will initially wear the SWIFT Cast for the whole of their waking day, and this will be adjusted as clinically appropriate. Outcomes Measures will be undertaken before randomization, six-weeks thereafter and six-months after stroke. Primary outcome will be walking speed. Secondary outcomes will include the Functional Ambulation Category and efficiency of gait (e.g. step-time symmetry). Structural brain imaging using magnetic resonance imaging (standard fluid attenuated inversion recovery and T1-weighted high-resolution ‘volume’ spoiled gradient) will be undertaken at baseline. The clinical efficacy analysis will use analysis of covariance. The relationship between clinical response to therapy and biomechanical data will use correlation and multivariate regression techniques as required. For neuroimaging data, the relationship to clinical response to therapy will be computed using voxel-based lesion-symptom mapping. An interaction test across groups will identify which voxels are associated with different mean levels of treatment efficacy.

Publisher

SAGE Publications

Subject

Neurology

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