Pain self-management plus nurse-led support in young adults with irritable bowel syndrome: Study protocol for a pilot randomized control trial

被引:15
|
作者
Cong, Xiaomei [1 ,2 ,3 ]
Ramesh, Divya [1 ]
Perry, Mallory [1 ]
Xu, Wanli [1 ]
Bernier, Katherine M. [1 ]
Young, Erin E. [1 ]
Walsh, Stephen [1 ]
Starkweather, Angela [1 ,2 ,4 ]
机构
[1] Univ Connecticut, Sch Nursing, 231 Glenbrook Rd, Storrs, CT 06269 USA
[2] Univ Connecticut, Ctr Adv Managing Pain, Storrs, CT USA
[3] Univ Connecticut, Inst Syst Genom, Farmington, CT USA
[4] Univ Connecticut, Ctr Accelerating Precis Pain Self Management P20, Storrs, CT USA
基金
美国国家卫生研究院;
关键词
genetics; gut microbiome; irritable bowel syndrome; pain; self-management; QUALITY-OF-LIFE; GUT MICROBIOME; SYMPTOMS; QUESTIONNAIRE; IBS; INTERVENTION; EPIDEMIOLOGY; ASSOCIATION; POPULATIONS; DISORDERS;
D O I
10.1002/nur.21862
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Irritable bowel syndrome (IBS) is a functional gut disorder that typically manifests in early adult years. IBS patients report that pain is the most distressing symptom with the greatest impact on quality of life. Pain-sensitivity genes and the gut microbiome may influence severity of symptoms as well as response to self-management (SM) interventions. Based on current understanding of the science of SM, pain neurophysiology, and the gut-brain axis, our team developed a pain SM intervention to be added to evidence-based self-management instruction to increase the individual's SM knowledge and skills (self-efficacy, self-regulation, and goal-setting). The purpose of this randomized controlled longitudinal pilot study is to examine the feasibility, acceptability, and preliminary effectiveness of the IBS-painSMintervention on IBS-pain SM behaviors and related health outcomes. A sample of 80 young adults (age 18-29 years old) will be recruited and randomly assigned to the experimental or control group. Both groups will receive 10 electronic video modules focused on IBS-pain SM knowledge and skills. The experimental group also will receive nurse-led one-on-one phone consultations to facilitate monitoring and problem-solving. All participants will be followed over 12 weeks. Primary outcomes will be measured at baseline, 6 weeks, and 12 weeks, including IBS-pain SM behaviors, quality of life, and well-being. The influence of pain-sensitivity genes and the gut microbiome on IBS-pain SM behaviors and health outcomes also will be assessed.
引用
收藏
页码:121 / 130
页数:10
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