TY - JOUR
T1 - Co-design and Consultation Ensure Consumer Needs Are Met
T2 - Building an eHealth Platform for Children with Inflammatory Bowel Disease
AU - Pipicella, Joseph Louis
AU - Vernon-Roberts, Angharad
AU - Dutt, Shoma
AU - Giles, Edward
AU - Day, Andrew S.
AU - Connor, Susan Jane
AU - Andrews, Jane Mary
N1 - Funding Information:
The authors would like to thank Stratos Technology Partners (518 Colombo Street, Christchurch Central City, Christchurch 8011, New Zealand) for assisting with software build, Dr Astrid Jane Williams (University of New South Wales, Medicine (SWS Clinical School), Sydney, New South Wales, Australia) for assisting with manuscript editing., and Prof Richard Blair Gearry (University of Otago Christchurch, Department of Medicine, Christchurch, New Zealand) for attending working group meetings and assisting with manuscript editing.
Funding Information:
Open Access funding enabled and organized by CAUL and its Member Institutions. The study received generous support from The Leona M. and Harry B. Helmsley Charitable Trust (Grant No. #2002-04267) and The Australian Government, Department of Education and Training: Research Training Program (RTP) Fees Offset Scholarship.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Background: Crohn’s Colitis Care is an adult inflammatory bowel disease eHealth system. Crohn’s Colitis Care required additional pediatric functionality to enable life-long records and mitigate transition inadequacies. Aim: This study describes and evaluates a consensus method developed to ensure consumer needs were met. Methods: Pediatric-specific functionality and associated resources considered important for inclusion were developed by a clinician consensus group. This group was divided into thematic subgroups and underwent two voting rounds. The content validity index was used to determine items reaching consensus. Children with inflammatory bowel disease and their parents were later shown a descriptive list of non-clinical inclusion topics proposed by the consensus group, and asked to vote on whether topic-related functionality and resources should be included. Results: The consensus process consulted 189 people in total (38 clinicians, 32 children with inflammatory bowel disease and 119 parents). There was agreement across all groups to incorporate functionality and resources pertaining to quality of life, mental health, self-management, and transition readiness; however, divergence was seen for general inflammatory bowel disease facts, your inflammatory bowel disease history, and satisfaction. Cost saw the greatest disparity, being less supported by consumers compared to clinicians. Over 75% of consumers agreed it would be okay for appointments to take longer for survey completion, and > 90% thought Crohn’s Colitis Care should allow consumers to ask their treating team questions. Conclusions: Widespread consumer co-design and consultation were important in unveiling differing perspectives to ensure Crohn’s Colitis Care was built to support both consumer and clinician perspectives. Graphical Abstract: Consumers collaborate to create a list of functionality and resources to be included in software (left), influencing the final product build (right). [Figure not available: see fulltext.].
AB - Background: Crohn’s Colitis Care is an adult inflammatory bowel disease eHealth system. Crohn’s Colitis Care required additional pediatric functionality to enable life-long records and mitigate transition inadequacies. Aim: This study describes and evaluates a consensus method developed to ensure consumer needs were met. Methods: Pediatric-specific functionality and associated resources considered important for inclusion were developed by a clinician consensus group. This group was divided into thematic subgroups and underwent two voting rounds. The content validity index was used to determine items reaching consensus. Children with inflammatory bowel disease and their parents were later shown a descriptive list of non-clinical inclusion topics proposed by the consensus group, and asked to vote on whether topic-related functionality and resources should be included. Results: The consensus process consulted 189 people in total (38 clinicians, 32 children with inflammatory bowel disease and 119 parents). There was agreement across all groups to incorporate functionality and resources pertaining to quality of life, mental health, self-management, and transition readiness; however, divergence was seen for general inflammatory bowel disease facts, your inflammatory bowel disease history, and satisfaction. Cost saw the greatest disparity, being less supported by consumers compared to clinicians. Over 75% of consumers agreed it would be okay for appointments to take longer for survey completion, and > 90% thought Crohn’s Colitis Care should allow consumers to ask their treating team questions. Conclusions: Widespread consumer co-design and consultation were important in unveiling differing perspectives to ensure Crohn’s Colitis Care was built to support both consumer and clinician perspectives. Graphical Abstract: Consumers collaborate to create a list of functionality and resources to be included in software (left), influencing the final product build (right). [Figure not available: see fulltext.].
KW - Consensus
KW - Inflammatory bowel diseases
KW - Outpatients
KW - Pediatrics
KW - Telemedicine
UR - http://www.scopus.com/inward/record.url?scp=85175058469&partnerID=8YFLogxK
U2 - 10.1007/s10620-023-08146-2
DO - 10.1007/s10620-023-08146-2
M3 - Article
C2 - 37897556
AN - SCOPUS:85175058469
SN - 0163-2116
VL - 68
SP - 4368
EP - 4380
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 12
ER -