Efficacy of digital health technologies in the management of inflammatory bowel disease: an umbrella review
- PMID: 40374487
- DOI: 10.1016/j.landig.2024.12.007
Efficacy of digital health technologies in the management of inflammatory bowel disease: an umbrella review
Abstract
The use of digital health technology (DHT) is increasing worldwide. Clinical trials assessing available health tools for the management of patients with inflammatory bowel disease (IBD) are sparse, with limited evidence-based outcome data. In this umbrella review, we investigated the effectiveness of DHT in the care of patients with IBD and identified areas for future research following the Joanna Briggs Institute methodology. Systematic reviews published between January, 2012, and September, 2024, were identified through searches across nine databases (Ovid Embase, Ovid MEDLINE, ProQuest PsycINFO, Epistemonikos, Cochrane, Health Evidence, DoPHER, PROSPERO, and CINAHL via EBSCO), and the results were imported into Covidence software. Inclusion criteria included systematic reviews of randomised controlled trials (RCTs) involving patients of all ages with Crohn's disease or ulcerative colitis, using DHT for diagnostics, treatment support, monitoring, self-management, or increasing participation in research studies, compared with standard care or alternative interventions. Outcomes included the efficacy and effectiveness of digital interventions, as reported in the studies. The primary outcome was clinical efficacy reported as one or more of the following: clinical response or remission, disease activity, flare-ups or relapses, and quality of life. Secondary outcomes included medication adherence, number of health-care visits, patient engagement (satisfaction and adherence or compliance with interventions), attendance for all terms of engagement, rate of interactions, knowledge improvement, psychological outcomes, and cost or cost-time effectiveness. The review protocol was registered in PROSPERO (registration number: CRD42023417525). AMSTAR-2 was used for methodological quality assessment. Nine relevant reviews were included, including five with meta-analyses comprising 13-19 RCTs in each review; four reviews were rated as high quality and five as critically low quality. DHT was not directly beneficial in achieving or maintaining clinical remission in IBD. In four trials, DHT use was associated with a reduced number of hospital attendances and increased treatment adherence, supporting its role as an adjuvant to standard clinical practice in IBD. Although current evidence from several RCTs and systematic reviews does not indicate better clinical outcomes with DHT in maintaining IBD remission and reducing relapse rates, DHT could be used as an adjuvant resource contributing towards treatment adherence and reducing hospital visits.
Copyright © 2025 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of interests JA is a scientific advisory board member for Orchard Therapeutics and is funded by a National Institute for Health and Care Research (NIHR) advanced fellowship. MG is a non-paid member of the Crohn’s in Childhood Research Association Advisor Board; member and previous chair of the Research Committee of the British Society of Paediatric Gastroenterology, Hepatology and Nutrition (BSPGHAN); member and previous chair of the Special Interest Group for Basic Science and Translational Research of ESPGHAN (European Society of Paediatric Gastroenterology, Hepatology and Nutrition); collaborator of a research project led by Cambridge University Hospitals and awarded a Helmsley’s Trust Grant in 2022; and collaborator of a study titled “Prime-P” at the Quadram Institute of Bioscience, which was awarded a Seedcorn Grant in 2023. MP is a non-paid board member of the non-profit and foundation MyCoach, a foundation that owns the content of myIBDcoach. NA received funding from the British Society of Gastroenterology (BSG), BSPGHAN, and CYMEDTECH; payment or honoraria from Janssen, AbbVie, and Takeda; and support from Eli Lilly to attend a conference. NA is also a member and previous chair of the BSG Adolescent and Young Persons Committee and a previous chair of the European Crohn’s and Colitis Organisation (ECCO) Epi-Committee. PN is the co-lead of the transition theme at the NIHR HealthTech Research centre in Paediatrics and Child Health. UK has received funding from AbbVie, Jannsen, Bristol Myers Squibb, Eli Lilly, Medtronic, and Takeda, as well as consulting fees and payment or honoraria from AbbVie, Jannsen, BMS, Eli Lilly, Medtronic, Takeda, Celltrion, Roche, and Pfizer. UK has participated in a Data Safety Monitoring Board or Advisory Board for AbbVie, Jannsen, Eli Lilly, Medtronic, Takeda, Roche, and Pfizer. UK is also a member of the ECCO committee. All other authors declare no competing interests.
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