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粪便失禁干预研究(FINS):有或无护士支持的自我管理手册信息对改善炎症性肠病患者的大便失禁情况:一项随机对照试验的研究方案

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.

作者信息

Norton Christine, Dibley Lesley B, Hart Ailsa, Duncan Julie, Emmanuel Anton, Knowles Charles H, Stevens Natasha, Terry Helen, Verjee Azmina, Kerry Sally, Hounsome Natalia

机构信息

Florence Nightingale Faculty of Nursing and Midwifery, King's College, 57 Waterloo Road, London, SE1 8WA, UK.

St Mark's Hospital, Watford Road, Harrow, HA1 3UJ, UK.

出版信息

Trials. 2015 Oct 6;16:444. doi: 10.1186/s13063-015-0962-0.

Abstract

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.

摘要

背景

炎症性肠病包括克罗恩病和溃疡性结肠炎,是一种终身性且目前无法治愈的疾病。它会引发急性肠道炎症发作,病程呈不可预测的复发-缓解型,伴有血性腹泻以及急需上厕所的情况。大便失禁是一个严重的社会和卫生问题,对生活质量、工作能力和社交能力都有重大影响。在普通人群中,2%-10%的成年人会出现大便失禁。炎症性肠病患者出现失禁的风险很高,高达74%的患者受其影响。此前尚无研究探讨针对这些患者的保守干预措施。

方法

这项随机对照试验将招募186名参与者,以回答研究问题:实施英国国家推荐的大便失禁逐步管理指导方法,是否能改善炎症性肠病患者的肠道控制能力和生活质量?我们与炎症性肠病患者合作,将该指导转化为一本关于失禁管理的特定病情信息手册。我们将随机分配参与者,使其接受该手册,或该手册加上与一名炎症性肠病专科护士进行的最多四次30分钟的会诊。符合条件的患者必须处于疾病缓解期且报告有失禁情况。随机分组后6个月的主要结局指标是圣马克失禁评分。其他结局指标包括生活质量、MY-MOP(通用工具:参与者设定两个干预目标,在基线时对目标进行评分,然后在干预后重新评分)以及EQ-5D-5L,以便计算质量调整生命年。分析将基于意向性分析原则。定性访谈将探讨参与者和医疗专业人员对干预措施的看法。

讨论

针对炎症性肠病的保守干预措施,高质量研究很少,针对大便失禁的研究则尚无。我们与患者合作设计了这项研究。对这种行为干预进行盲法处理是不可能的,但我们的自我报告结局指标具有一定程度的客观性。仅手册组和手册加护士组之间存在真正的平衡,该研究将确定护士的额外支持是否是实施建议的关键要素。

试验注册

clinitrials.gov.uk:NCT02355834(注册日期:2014年12月12日)。方案版本:4.0。2015年4月8日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec37/4594995/b2ca25cc418a/13063_2015_962_Fig1_HTML.jpg

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