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炎症性肠病综合自我管理干预(CSM-IBD):一项试点随机对照试验的方案

A Comprehensive Self-Management Intervention for Inflammatory Bowel Disease (CSM-IBD): Protocol for a Pilot Randomized Controlled Trial.

作者信息

Kamp Kendra, Clark-Snustad Kindra, Yoo Linda, Winders Samantha, Cain Kevin, Levy Rona L, Dey Neelendu, Lee Scott, Keefer Laurie, Heitkemper Margaret

机构信息

Department of Biobehavioral Nursing and Health Informatics, School of Nursing, University of Washington, Seattle, WA, United States.

Division of Gastroenterology, School of Medicine, University of Washington, Seattle, WA, United States.

出版信息

JMIR Res Protoc. 2023 Jun 7;12:e46307. doi: 10.2196/46307.

Abstract

BACKGROUND

Despite pharmacological treatment, individuals with inflammatory bowel disease (IBD) experience a variety of symptoms, including abdominal pain, fatigue, anxiety, and depression. Few nonmedical self-management interventions are available for people with IBD. A validated comprehensive self-management (CSM) intervention is effective for patients with irritable bowel syndrome who can have symptoms similar to those of individuals with IBD. We created a modified CSM intervention tailored to individuals with IBD (CSM-IBD). The CSM-IBD is an 8-session program delivered over 8-12 weeks with check-ins with a registered nurse.

OBJECTIVE

The primary objective of this pilot study is to determine the feasibility and acceptability of study procedures and the CSM-IBD intervention and to evaluate preliminary efficacy on quality of life and daily symptoms for a future randomized controlled trial. Additionally, we will examine the association of socioecological, clinical, and biological factors with symptoms at baseline and response to intervention.

METHODS

We are conducting a pilot randomized controlled trial of the CSM-IBD intervention. Participants aged 18-75 years who are experiencing at least 2 symptoms are eligible for inclusion. We plan to enroll 54 participants who will be randomized (2:1) into the CSM-IBD program or usual care. Patients in the CSM-IBD program will have 8 intervention sessions. Primary study outcomes include the feasibility of recruitment, randomization, and data or sample collection, as well as the acceptability of study procedures and interventions. Preliminary efficacy outcome variables include quality of life and symptoms. Outcomes data will be assessed at baseline, immediately post intervention, and 3 months post intervention. Participants in the usual care group will have access to the intervention after study participation.

RESULTS

This project is funded by the National Institutes of Nursing Research and reviewed by the University of Washington's institutional review board. Recruitment began in February 2023. As of April 2023, we have enrolled 4 participants. We expect the study to be completed by March 2025.

CONCLUSIONS

This pilot study will evaluate the feasibility and efficacy of a self-management intervention (a web-based program with weekly check-ins with a registered nurse) that aims to improve symptom management in individuals with IBD. In the long term, we aim to validate a self-management intervention to improve patient quality of life, reduce direct and indirect costs related to IBD, and be culturally appropriate and accessible, particularly in rural and underserved communities.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05651542; https://clinicaltrials.gov/ct2/show/NCT05651542.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/46307.

摘要

背景

尽管接受了药物治疗,但炎症性肠病(IBD)患者仍会出现多种症状,包括腹痛、疲劳、焦虑和抑郁。针对IBD患者的非医疗自我管理干预措施很少。一种经过验证的综合自我管理(CSM)干预措施对肠易激综合征患者有效,这些患者可能有与IBD患者相似的症状。我们创建了一种针对IBD患者量身定制的改良CSM干预措施(CSM-IBD)。CSM-IBD是一个为期8节的课程,在8至12周内完成,并与注册护士进行签到。

目的

这项初步研究的主要目的是确定研究程序和CSM-IBD干预措施的可行性和可接受性,并评估其对生活质量和日常症状的初步疗效,为未来的随机对照试验提供依据。此外,我们将研究社会生态、临床和生物学因素与基线症状及干预反应之间的关联。

方法

我们正在进行一项CSM-IBD干预措施的初步随机对照试验。年龄在18至75岁且至少出现2种症状的参与者符合纳入条件。我们计划招募54名参与者,他们将被随机分配(2:1)到CSM-IBD项目或常规护理组。CSM-IBD项目的患者将接受8次干预课程。主要研究结果包括招募、随机分组以及数据或样本收集的可行性,以及研究程序和干预措施的可接受性。初步疗效结果变量包括生活质量和症状。结果数据将在基线、干预后立即以及干预后3个月进行评估。常规护理组的参与者在研究结束后可以使用该干预措施。

结果

该项目由美国国立护理研究所以及华盛顿大学机构审查委员会资助。招募工作于2023年2月开始。截至2023年4月,我们已招募了4名参与者。我们预计该研究将于2025年3月完成。

结论

这项初步研究将评估一种自我管理干预措施(一个基于网络的项目,每周与注册护士进行签到)的可行性和疗效,该措施旨在改善IBD患者的症状管理。从长远来看,我们旨在验证一种自我管理干预措施,以提高患者的生活质量,降低与IBD相关的直接和间接成本,并在文化上具有适宜性和可及性,特别是在农村和服务不足的社区。

试验注册

ClinicalTrials.gov NCT05651542;https://clinicaltrials.gov/ct2/show/NCT05651542。

国际注册报告识别码(IRRID):PRR1-10.2196/46307。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359e/10285620/5eaf10b25a56/resprot_v12i1e46307_fig1.jpg

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