Mobile Self-Management of Irritable Bowel Syndrome for Adolescents

Completed · Not applicable

Conditions studied: Irritable Bowel Syndrome, Abdominal Pain

In brief

The objective of the proposed research is to conduct user testing of a mobile-based self-management support intervention for adolescents and young adults with Irritable Bowel Syndrome (IBS), a chronic digestive condition. The application (app; BodiMojo Buddy) uses a virtual coach that can serve to increase patient engagement through interactive skill-building, self-care, and mindfulness-based cognitive behavioral activities. If the BodiMojo Buddy mobile app is successful, it will have a significant public health impact by providing a mobile resource to the 10-15% of the US population who suffer from IBS and potentially improving health outcomes and reducing significant costs to the US healthcare system. Study participation involves participants downloading and using the app for 30 days. During the 30 days, participants will interact with the app by inputting their current mood, receiving supportive feedback from the app, reading messages, and doing brief activities (such as relaxation activities, etc.). Before and after the 30 days of user testing, participants will complete a few brief questionnaires about their behavior, how their symptoms affect their life, and how they receive support from others. These questions will take around 20 minutes to complete at each administration.

Key facts

Study ID: NCT03138980
Run by: University of California, Los Angeles
People needed: 26
Starts: 2016-01-30
Expected to finish: 2016-09-22
Last updated by the study team: 2017-06-27

Who can join

Age: 13 and older, up to 21. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Age 13-21 years
For adolescents: Parent-reported physician diagnosis of IBS, using pediatric Rome III diagnostic criteria for functional gastrointestinal disorders. For young adults: self-reported physician diagnosis of IBS using Rome III diagnostic criteria, or meeting criteria for IBS or functional abdominal pain as determined during phone screening.
Have daily use of an iPhone or iPad that meets the following technical specifications: at least iOS 8; for iPhones, must be iPhone 5 or above.
Able and willing to give informed assent/consent and comply with study requirements
Have one caregiver willing and able to participate in the study [only for 13-17 year olds]

You may not qualify if…

Inability to provide informed assent/permission/consent
Inability to read, speak, and understand English (because the app content/parent guides are written in English, as are the measures being used in the study)

Where it is running

UCLA Pediatric Pain Program Research Offices — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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