Crohn Disease Clinical Trial
— EMBODYOfficial title:
The Effects of a Mindfulness Based Intervention on IBD Disability
NCT number | NCT05944068 |
Other study ID # | S67980 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 6, 2024 |
Est. completion date | June 30, 2025 |
EMBODY (Effects of a Mindfulness Based interventiOn on ibD disabilitY) aims to evaluate the effects of a mindfulness based intervention on a broad number of disease related disability dimensions in patients with Crohn's disease (abdominal pain, regulation defecation, joint pain, energy, emotions, body image, interpersonal interactions, education and work, sexual function, sleep). Besides, the investigators will measure the effect of the intervention on depression, anxiety, stress, disease acceptance and perceived control as well as (biomarkers of) disease activity. It will be a prospective, randomized-controlled, monocentric, superiority trial using a waiting list with treatment as usual as control arm. Half of the patients will immediately start the mindfulness based intervention (early intervention group). In the other half, there will be a waiting time of 6 months before starting the mindfulness based intervention (late intervention or control group). Clinical disease activity (two-item patient reported outcome (PRO2)), faecal calprotectin and C-reactive protein (CRP) will be collected throughout the trial (pre-, during and post-intervention). The investigators will measure IBD-related disability through the IBD-Disk, a tool for assessing the impact of the disease on ten different dimensions of everyday life dimensions. Depression, anxiety and Stress will be investigated via the Depression Anxiety Stress Scale Short Form (DASS21). Disease acceptance and perceived control will be measured using the Subjective Health Experience (SHE) model. Evolution of the different variables will be compared between both groups (ANOVA).
Status | Recruiting |
Enrollment | 50 |
Est. completion date | June 30, 2025 |
Est. primary completion date | May 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Voluntary written informed consent of the participant has been obtained prior to any screening procedures 2. Males and females 18-80 years old. 3. Patients with a diagnosis of Crohn's disease based on radiology, endoscopy and/or histology 4. Patients with more than one year of follow-up since diagnosis 5. Patients having internet or smartphone access 6. Patients being fluent in Dutch Exclusion Criteria: 1. Participation in an interventional Trial with an investigational medicinal product (IMP) or device 2. Patients that initiated a new IBD medication (steroids, thiopurines, methotrexate, biologicals or small molecules) in the past three months 3. Patients in whom a major surgery or acute surgery with hospitalization can be expected during the complete study period 4. Patients with a present or past psychiatric disease diagnosis (psychosis, bipolar disease, substance abuse) 5. Patients using psychotropic medication 6. Patients with former experience of mindfulness training |
Country | Name | City | State |
---|---|---|---|
Belgium | University Hospitals Leuven | Leuven |
Lead Sponsor | Collaborator |
---|---|
Universitaire Ziekenhuizen KU Leuven |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Evolution of C-reactive protein and fecal calprotectin over time | Evolution of CRP over time. Evolution of faecal calprotectin over time. | 12 months | |
Primary | The median change in the IBD-related disability index by month 3 | This study will evaluate if a mindfulness based intervention can improve IBD-related disability, measured through the IBD Disk. Patients are asked to rate each item on a scale from 0 to 10 (0 = absolutely disagree, 10 = absolutely agree), resulting in a total score ranging from 0 to 100. A higher score represents higher IBD-related disability. | 6 months | |
Secondary | The median change in separate components of the IBD-related disability index, perceived stress, perceived control and disease acceptante by month 3 | The median change in the seperate components of the IBD-related disability index by month 3.
Each item is rated on a scale from 0 to 10 (0 = absolutely disagree, 10 = absolutely agree). A higher score represents higher IBD-related disability. The median change in the depression/anxiety/stress scale of the DASS21 by month 3. Each of the three scales contains 7 items. Items are rated on 4-point severity/frequency scales. Higher scores represent higher probability of depression, anxiety and/or stress. The median change in the disease acceptance/perceived control component of the SHE model by month 3. The SHE model contains 6 questions with a scale from 1 to 7 (1=fully agree, 7=fully disagree). Higher scores represent higher perceived control/acceptance. |
6 months |
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