脑卒中后失语症的解决方案集中短期治疗(SOFIA试验):一项可行性随机对照试验方案

S. Northcott, A. Simpson, Shirley A. Thomas, S. Hirani, C. Flood, K. Hilari
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引用次数: 9

摘要

背景:大约四分之一的中风患者会出现失语症,这是一种语言障碍。患有失语症的人有变得抑郁和孤立的风险。有有限的证据表明,有效的干预措施,以提高心理健康的客户群体。一种潜在的干预方法是专注于解决方案的简短疗法(SFBT),它通过关注一个人的技能和资源,而不是他们的缺陷,来支持一个人建立有意义的、可实现的改变。SOFIA试验旨在探讨SFBT对不同失语症患者(包括严重失语症患者)的可接受性,并评估开展未来决定性试验的可行性,调查临床和成本效益。方法:本试验为单盲、随机、等候名单对照可行性试验,采用嵌套定性研究和试点经济评价,比较SFBT加常规护理与单独常规护理。该研究将招募32名卒中后≥6个月的失语症患者。所有参与者将在基线、随机化后3个月和6个月由盲法评估者评估心理社会结果。参与者将被随机分配到干预组(随机化后立即开始干预)或等候组(随机化后六个月开始干预)。等待名单组将在随机分组后9个月进行额外评估。干预包括六个SFBT会话,由言语和语言治疗师在三个月内提供。参与者和治疗师也将参与深入访谈,探讨他们的研究经验。试点经济评估将使用EQ-5D-5L测量方法和经过调整的客户服务收据清单。失语症患者参与了试验的设计和监测。讨论:鉴于失语症患者的抑郁和孤立程度很高,有必要研究有效的干预措施,以增强失语症患者的心理健康。试验注册:ClinicalTrials.gov NCT03245060 10/08/2017。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solution Focused brief therapy In post-stroke Aphasia (SOFIA Trial): protocol for a feasibility randomised controlled trial
Background: Around a quarter of people post stroke will experience aphasia, a language disability. Having aphasia places someone at risk of becoming depressed and isolated. There is limited evidence for effective interventions to enhance psychological well-being for this client group. A potential intervention is Solution Focused Brief Therapy (SFBT), which supports a person to build meaningful, achievable change through focusing on a person’s skills and resources rather than their deficits. The SOFIA Trial aims to explore the acceptability of SFBT to people with varying presentations of aphasia, including severe aphasia, and to assess the feasibility of conducting a future definitive trial investigating clinical and cost effectiveness. Methods: The trial is a single-blind, randomised, wait-list controlled feasibility trial with nested qualitative research and pilot economic evaluation comparing SFBT plus usual care to usual care alone. The study will recruit 32 participants with aphasia who are ≥6 months post stroke. All participants will be assessed on psychosocial outcome measures at baseline, three, and six months post randomisation by assessors blinded to treatment allocation. Participants will be randomly assigned to intervention group (start intervention immediately post randomisation) or wait-list group (start intervention six months post randomisation). Wait-list group will additionally be assessed nine months post randomisation. The intervention consists of up to six SFBT sessions delivered over three months by speech and language therapists. Participants and therapists will also take part in in-depth interviews exploring their experiences of the study. The pilot economic evaluation will use the EQ-5D-5L measure and an adapted Client Service Receipt Inventory. People with aphasia have been involved in designing and monitoring the trial. Discussion: Given the high levels of depression and isolation, there is a need to investigate effective interventions that enhance the psychological wellbeing of people with aphasia. Trial registration: ClinicalTrials.gov NCT03245060 10/08/2017.
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