The Effects of a Mindfulness Based Intervention on IBD Disability (EMBODY)
Crohn Disease
About this trial
This is an interventional supportive care trial for Crohn Disease
Eligibility Criteria
Inclusion Criteria: Voluntary written informed consent of the participant has been obtained prior to any screening procedures Males and females 18-80 years old. Patients with a diagnosis of Crohn's disease based on radiology, endoscopy and/or histology Patients with more than one year of follow-up since diagnosis Patients having internet or smartphone access Patients being fluent in Dutch Exclusion Criteria: Participation in an interventional Trial with an investigational medicinal product (IMP) or device Patients that initiated a new IBD medication (steroids, thiopurines, methotrexate, biologicals or small molecules) in the past three months Patients in whom a major surgery or acute surgery with hospitalization can be expected during the complete study period Patients with a present or past psychiatric disease diagnosis (psychosis, bipolar disease, substance abuse) Patients using psychotropic medication Patients with former experience of mindfulness training
Sites / Locations
- University Hospitals Leuven
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Early intervention group
Late intervention group
This group will receive the intervention immediately after baseline.
This group will receive the intervention 6 months after baseline, in psychological studies called the waiting list group