Clinical Hypnosis in Pediatric Crohn's Disease (HypnoCrohns)
Pediatric Crohns Disease
About this trial
This is an interventional treatment trial for Pediatric Crohns Disease focused on measuring hypnosis, inflammatory bowel disease, mind-body, brain-gut, hypnotherapy, quality of life, psychosocial
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed with Crohn's disease at least 3 months prior to enrollment
- Inactive, mild, or moderate disease activity by Improve Care Now Physician's Global Assessment (ICN PGA) at most recent GI clinic visit
- Ages 12-18 years at time of enrollment
- English-speaking and with the normal cognitive development required to understand the verbal instructions/suggestions provided in the hypnosis session/audio recordings and to understand and complete the written surveys
- Has daily access to an electronic device (ex. smartphone, computer) that can receive text messages or e-mail, on which online surveys can be completed, and on which the participant can access and listen to audio recordings.
Exclusion Criteria:
- Patients diagnosed with Crohn's disease less than 3 months prior to enrollment
- Severe disease activity per ICN PGA at most recent GI clinic visit
- Age < 12 years or > 18 years
- Non-English speaking or having a cognitive disability that precludes understanding the verbal instructions/suggestions provided in the hypnosis session/audio recordings and the completion of written surveys
- Lacks daily access to an electronic device (ex. smartphone, computer) that can receive text messages or e-mail, on which online surveys can be completed, and on which the participant can access and listen to audio recordings.
Sites / Locations
- Vanderbilt University Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Hypnosis Intervention
Waitlist Control
The intervention is clinical hypnosis--a single in-person session followed by instructions to listen to audio recordings at home. The sessions consist of the provider's voice guiding the participant into a relaxed and focused state and providing therapeutic suggestions--for example, to replace discomfort with a more pleasant sensation, to ease anxiety, and to increase energy.
This group will serve as a control comparison and be offered the intervention after control data collection is complete.