A study of prisms and therapy in attention loss after stroke (SPATIAL): A feasibility randomised controlled trial

Author:

Longley Verity1ORCID,Woodward-Nutt Kate2,Turton Ailie J.3,Stocking Katie4,Checketts Matthew2,Bamford Ann2,Douglass Emma3,Taylor Julie5,Woodley Julie3,Moule Pam3,Vail Andy4,Bowen Audrey2ORCID

Affiliation:

1. Faculty of Health and Education, Manchester Metropolitan University, Manchester, UK

2. Geoffrey Jefferson Brain Research Centre, The Manchester Academic Health Science Centre, Northern Care Alliance & University of Manchester, Manchester, UK

3. School for Health and Social Wellbeing, University of the West of England, Bristol, UK

4. Centre for Biostatistics, The Manchester Academic Health Science Centre, Northern Care Alliance & University of Manchester, Manchester, UK

5. Dorothy House Hospice Care, Bradford-on-Avon, UK

Abstract

Objective Investigate feasibility and acceptability of prism adaptation training for people with inattention (spatial neglect), early after stroke, during usual care. Design Phase II feasibility randomised controlled trial with 3:1 stratified allocation to standard occupational therapy with or without intervention, and nested process evaluation. Setting Ten hospital sites providing in-patient stroke services. Participants Screened positive for inattention more than one-week post-stroke; informal carers. Occupational therapists participated in qualitative interviews. Intervention Adjunctive prism adaptation training at the start of standard occupational therapy sessions for three weeks. Main measures Feasibility measures included recruitment and retention rates, intervention fidelity and attrition. Outcomes collected at baseline, 3 weeks and 12 weeks tested measures including Nottingham Extended Activities of Daily Living Scale. Acceptability was explored through qualitative interviews and structured questions. Results Eighty (31%) patients were eligible, 57 (71%) consented, 54 randomised (40:13, +1 exclusion) and 39 (74%) completed 12-week outcomes. Treatment fidelity was good: participants received median eight intervention sessions (IQR: 5, 12) lasting 4.7 min (IQR: 4.1, 5.0). All six serious adverse events were unrelated. There was no signal that patients allocated to intervention did better than controls. Twenty five of 35 recruited carers provided outcomes with excellent data completeness. Therapists, patients and carers found prism adaptation training acceptable. Conclusions It is feasible and acceptable to conduct a high-quality definitive trial of prism adaptation training within occupational therapy early after stroke in usual care setting, but difficult to justify given no sign of benefit over standard occupational therapy. Clinical trial registration https://www.isrctn.com/ Ref ISRCTN88395268.

Funder

Stroke Association

University of Manchester

National Institute for Health Research

Publisher

SAGE Publications

Subject

Rehabilitation,Physical Therapy, Sports Therapy and Rehabilitation

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