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首页> 外文期刊>Trials >Faecal incontinence intervention study (FINS): self-management booklet information with or without nurse support to improve continence in people with inflammatory bowel disease: study protocol for a randomized controlled trial
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Faecal incontinence intervention study (FINS): self-management booklet information with or without nurse support to improve continence in people with inflammatory bowel disease: study protocol for a randomized controlled trial

机译:粪便失禁干预研究(FINS):有或没有护士支持的自我管理小册子信息,以改善炎症性肠病患者的节制:一项随机对照试验的研究方案

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Background Inflammatory bowel disease, comprising Crohn’s disease and ulcerative colitis, is a life-long currently incurable illness. It causes bouts of acute intestinal inflammation, in an unpredictable relapsing-remitting course, with bloody diarrhoea and extreme urgency to access a toilet. Faecal incontinence is a devastating social and hygiene problem, impacting heavily on quality of life and ability to work and socialise. Faecal incontinence affects 2–10 % of adults in the general population. People with inflammatory bowel disease have a high risk of incontinence with up to 74 % affected. No previous study has explored conservative interventions for these patients. Methods This randomised controlled trial will recruit 186 participants to answer the research question: does implementation of the UK nationally recommended guidance approach to stepwise management of faecal incontinence improve bowel control and quality of life in people with inflammatory bowel disease? We have worked with people with inflammatory bowel disease to translate this guidance into a condition-specific information booklet on managing incontinence. We will randomise participants to receive the booklet, or the booklet plus up to four 30-minute sessions with an inflammatory bowel disease specialist nurse. To be eligible, patients must be in disease remission and report incontinence. The primary outcome measure at 6 months after randomisation is the St Mark’s incontinence score. Other outcomes include quality of life, MY-MOP (generic tool: participants set two goals for intervention, grading goals at baseline and then re-scoring after intervention) and EQ-5D-5 L to enable calculation of quality-adjusted life years. Analysis will be on an intention-to-treat basis. Qualitative interviews will explore participant and health professionals’ views on the interventions. Discussion Few high-quality studies of conservative interventions in inflammatory bowel disease, and none for faecal incontinence, have been conducted. We have collaborated with patients to design this study. Blinding to this behavioural intervention is not possible, but our self-report outcome measures with a degree of objectivity. There is genuine equipoise between the booklet only and booklet plus nurse arms, and the study will determine if additional support from a nurse is a crucial element in implementing advice. Trial registration clinitrials.gov.uk: NCT02355834 (Date of registration: 12 December 2014). Protocol version: 4.0. 08.04.15
机译:背景技术包括克罗恩氏病和溃疡性结肠炎在内的炎症性肠病是一生中目前无法治愈的疾病。它会在无法预测的复发-缓解过程中引起急性肠道发炎,并伴有血性腹泻和极度紧急进入厕所的危险。粪便失禁是一个破坏性的社会和卫生问题,严重影响生活质量以及工作和社交能力。粪便失禁影响普通人群中2-10%的成年人。炎症性肠病患者有较高的失禁风险,受影响的人群高达74%。以前没有研究探索针对这些患者的保守干预措施。方法该随机对照试验将招募186名参与者,以回答研究问题:英国国家推荐的指导性方法逐步控制粪便失禁是否会改善炎症性肠病患者的肠道控制和生活质量?我们与炎症性肠病患者合作,将本指南转化为关于失禁的特定病情手册。我们将随机分配参与者以接受小册子,或小册子以及炎症性肠病专科护士进行的最多四次30分钟的课程。为了符合条件,患者必须处于疾病缓解状态并报告失禁。随机分配后6个月的主要结局指标是圣马克的失禁评分。其他结果包括生活质量,MY-MOP(通用工具:参与者设定两个干预目标,在基线时对目标定级,然后在干预后重新评分)和EQ-5D-5 L,以计算质量调整的生命年。分析将以意向为基础。定性访谈将探讨参与者和卫生专业人员对干预措施的看法。讨论很少有关于炎症性肠病的保守干预的高质量研究,也没有针对粪便失禁的研究。我们已经与患者合作设计了这项研究。这种行为干预是不可能的,但是我们的自我报告结果在一定程度上具有客观性。仅小册子和小册子加护士手臂之间就有真正的平衡,这项研究将确定护士的额外支持是否对实施建议至关重要。试用注册clinitrials.gov.uk:NCT02355834(注册日期:2014年12月12日)。协议版本:4.0。 15.04.15

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