A Study to Evaluate the Impact of Care4Today® IBD, a Smart System to Facilitate the Management of Crohn's Disease by Patients and Health Care Providers
NCT ID: NCT04232228
Last Updated: 2025-04-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
32 participants
OBSERVATIONAL
2020-02-07
2022-04-04
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Participants with Crohn's Disease (CD)
Adult participants with moderate to severe CD who agree to be part of the study and who fit the inclusion/exclusion criteria and use Care4Today inflammatory bowel disease (C4T IBD) alongside standard of care (SOC) at participating centers will be observed. Data available per clinical practice and via the C4T IBD application will be collected within this study. Participants will also be asked to complete questionnaires that are sent directly to the patients, which are not completed as part of clinical practice or via the application. Relevant data will be collected by prospectively following participants from the index date for 12 months, and also by retrospectively collecting data for the 6-month period prior to the index date from participant's medical records. Index is the activation date of C4T IBD application in participant's smartphone.
No intervention
No intervention was used in this study.
Interventions
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No intervention
No intervention was used in this study.
Eligibility Criteria
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Inclusion Criteria
* Participants with at least 6 months of continuous care in the study centre prior to index date
* Participants who have agreed to install Care4Today® inflammatory bowel disease (C4T IBD) on their iOS or android smartphone as part of their management of CD
* Participants providing informed written consent to participate in the study from the date of activation (including installation and linkage to HCP web interface) of the C4T IBD app on his/her smartphone
Exclusion Criteria
* Participants in remission for over 2 years as documented in their medical records
* Participants participating in an interventional clinical trial
* Participants participating in an observational study where the protocol interferes with the C4T study in the opinion of the principal investigator at each site
* Participants with insufficient command of English to interact effectively with C4T IBD and complete the study questionnaires in the opinion of the principal investigator at each site
* Participants unable or unwilling to provide their informed written consent to participate in the study
18 Years
ALL
No
Sponsors
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Janssen-Cilag Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Janssen-Cilag Ltd. Clinical Trial
Role: STUDY_DIRECTOR
Janssen-Cilag Ltd.
Locations
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Leeds Teaching Hospitals NHS Trust
Leeds, , United Kingdom
Countries
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Other Identifiers
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CNTO1275CRD4033
Identifier Type: OTHER
Identifier Source: secondary_id
CR108721
Identifier Type: -
Identifier Source: org_study_id
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