Protocol for a pilot randomised controlled trial of mindfulness-based cognitive therapy in youth with inflammatory bowel disease and depression

被引:7
|
作者
Ewais, Tatjana [1 ,2 ]
Begun, Jake [1 ,3 ]
Kenny, Maura [4 ,5 ]
Chuang, Kai-Hsiang [6 ]
Barclay, Johanna [3 ]
Hay, Karen [7 ]
Kisely, Steve [2 ,8 ]
机构
[1] Mater Misericordiae Brisbane Ltd, Mater Young Adult Hlth Ctr, South Brisbane, Qld, Australia
[2] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[3] Univ Queensland, Mater Res Inst, Brisbane, Qld, Australia
[4] Univ Adelaide, Fac Hlth & Med Sci, Adelaide, SA, Australia
[5] Mindfulness Training Inst, Teaching Fac, Sydney, NSW, Australia
[6] Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia
[7] QIMR Berghofer Med Res Inst, Stat Unit, Herston, Qld, Australia
[8] Metro South Hosp & Hlth Serv, Princess Alexandra Hosp, Woolloongabba, Qld, Australia
来源
BMJ OPEN | 2019年 / 9卷 / 04期
关键词
POSTTRAUMATIC GROWTH INVENTORY; ANXIETY; LONG; CONNECTIVITY; METAANALYSIS; GENETICS; EFFICACY; RELAPSE;
D O I
10.1136/bmjopen-2018-025568
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Inflammatory bowel disease (IBD) is a chronic autoinflammatory disease of the gastrointestinal tract with peak age of onset during adolescence and young adulthood. Adolescents and young adults (AYAs) with IBD experience higher depression rates compared with peers who are well or have other chronic conditions. Mindfulness-based interventions are of particular interest because of their potential to improve both the course of IBD and depression. Methods and analysis This study is a parallel design, single-blind, pilot randomised controlled trial (RCT) of mindfulness-based cognitive therapy (MBCT) in AYAs with IBD and depression. The trial aims to recruit 64 participants who will be randomly allocated to MBCT or treatment as usual. The primary outcome measure is the depression subscale score from the Depression, Anxiety and Stress Scale. Secondary outcomes include anxiety, stress, post-traumatic growth, IBD-related quality of life, illness knowledge, medication adherence, mindfulness, IBD activity, inflammatory markers, microbiome and brain neuroconnectivity changes. All outcomes other than neuroimaging will be collected at three time points: at baseline, at therapy completion and at 20 weeks. Neuroimaging will be conducted at baseline and at therapy completion. Mixed-effects linear and logistic regression modelling will be used to analyse continuous and dichotomous outcomes, respectively. Participants' experiences will be explored through focus groups, and thematic analysis will be used to generate relevant themes. Ethics and dissemination The protocol has been approved by the Mater Hospital Human Research Ethics Committee (HREC) and University of Queensland HREC. Trial findings will be published in peer-reviewed journals and will be presented at scientific conferences.
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页数:8
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