Protocol for a pilot randomised controlled trial of mindfulness-based cognitive therapy in youth with inflammatory bowel disease and depression.
Study Goal
The researchers aimed to evaluate the effectiveness of mindfulness-based cognitive therapy (MBCT) in reducing depression and improving IBD-related outcomes in adolescents and young adults with IBD.
Results Summary
The study is a pilot RCT assessing MBCT's impact on depression, anxiety, stress, IBD-related quality of life, and other secondary outcomes, but results are not yet available (pre-results).
Population
Adolescents and young adults (AYAs) with inflammatory bowel disease (IBD) and depression.
Effective Dosage
Not specified
Duration
Intervention duration not explicitly stated, but outcomes are measured at baseline, therapy completion, and 20 weeks.
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
mindfulness-based cognitive therapy (MBCT) | increase | the course of IBD | Adolescents and young adults (AYAs) with IBD | - | are of particular interest because of their potential to improve | #1 |
mindfulness-based cognitive therapy (MBCT) | increase | depression | Adolescents and young adults (AYAs) with IBD | - | are of particular interest because of their potential to improve | #2 |
mindfulness-based cognitive therapy (MBCT) | neutral | depression subscale score from the Depression, Anxiety and Stress Scale | AYAs with IBD and depression | - | will be used to analyse | #3 |
mindfulness-based cognitive therapy (MBCT) | neutral | anxiety | AYAs with IBD and depression | - | will be used to analyse | #4 |
mindfulness-based cognitive therapy (MBCT) | neutral | stress | AYAs with IBD and depression | - | will be used to analyse | #5 |
mindfulness-based cognitive therapy (MBCT) | neutral | post-traumatic growth | AYAs with IBD and depression | - | will be used to analyse | #6 |
mindfulness-based cognitive therapy (MBCT) | neutral | IBD-related quality of life | AYAs with IBD and depression | - | will be used to analyse | #7 |
mindfulness-based cognitive therapy (MBCT) | neutral | illness knowledge | AYAs with IBD and depression | - | will be used to analyse | #8 |
mindfulness-based cognitive therapy (MBCT) | neutral | medication adherence | AYAs with IBD and depression | - | will be used to analyse | #9 |
mindfulness-based cognitive therapy (MBCT) | neutral | mindfulness | AYAs with IBD and depression | - | will be used to analyse | #10 |
mindfulness-based cognitive therapy (MBCT) | neutral | IBD activity | AYAs with IBD and depression | - | will be used to analyse | #11 |
mindfulness-based cognitive therapy (MBCT) | neutral | inflammatory markers | AYAs with IBD and depression | - | will be used to analyse | #12 |
mindfulness-based cognitive therapy (MBCT) | neutral | microbiome | AYAs with IBD and depression | - | will be used to analyse | #13 |
mindfulness-based cognitive therapy (MBCT) | neutral | brain neuroconnectivity changes | AYAs with IBD and depression | - | will be used to analyse | #14 |
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. TRIAL REGISTRATION NUMBER: ACTRN12617000876392, U1111-1197-7370; Pre-results.