GUIA: a digital platform to facilitate result disclosure in genetic counseling
Sabrina A. SuckieliD, Jaqueline A. Odgis, Katie M. GallagheriD, Jessica RodrigueziD, Dana L. WatnickiD, Gabrielle BertieriD, Monisha SebastiniD, Nicole M. Yelton, Estefany María, Jessenia Lopez, Michelle Branco RamosiD, Nicole KellyiD, Nehama Teitelman, Faygel Beren, Tom Kaszemacher, Kojo Davis, Irma Laguerre, Lynne D. RichardsoniD, George A. DíaziD, Nathaniel Michael PearsoniD, Stephen B. EllisiD, Christian StolteiD, Mimsie Robinson, Patricia KovatchiD, Carol R. HorowitziD, , Eimear E. KennyiD
Abstract
PurposeUse of genomic sequencing is increasing at a pace that requires technological solutions to effectively meet the needs of a growing patient population. We developed GUIA, a web-based application, to enhance the delivery of genomic results and related clinical information to patients and families. MethodsGUIA development occurred in 5 phases: formative research, content development, user interface design, stakeholder/community member input, and web application development. Development was informed by qualitative research involving parents (N=22) whose children underwent genomic testing. Participants enrolled in the NYCKidSeq pilot study (N=18) completed structured feedback interviews post-result disclosure using GUIA. Genetic specialists, researchers, patients, and community stakeholders provided their perspectives on GUIAs design to ensure technical, cultural, and literacy appropriateness. ResultsNYCKidSeq participants responded positively to the use of GUIA to deliver their childrens results. All participants (N=10) with previous experience with genetic testing felt GUIA improved result disclosure, and 17 (94%) participants said the content was clear. ConclusionsGUIA communicates complex genomic information in an understandable and personalized manner. Initial piloting demonstrated GUIAs utility for families enrolled NYCKidSeq pilot study. Findings from the NYCKidSeq clinical trial will provide insight into GUIAs effectiveness in communicating results among diverse, multilingual populations.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 28
- FWCI
- 3.25
- Field percentile
- top 7%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The NYCKidSeq randomized controlled trial: Impact of GUIA digitally enhanced genetic counseling in racially and ethnically diverse families
Sabrina A. Suckiel, Nicole Kelly, … Eimear E. Kenny·medRxiv·Jul 5, 2023
- The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children
Jacqueline A. Odgis, Katie M. Gallagher, … Eimear E. Kenny·TrialsPeer-reviewed·Jan 14, 2021
- When to return genomic newborn screening results: health care professional perspectives
Anna C. F. Lewis, Adam H. Buchanan, … Ingrid A. Holm·medRxiv·Sep 7, 2026
- Developing clinician-centred design principles for Genomic Test Reports in Pakistan
Momal Agha, Faisal F. Khan·medRxiv·Dec 3, 2023
- Information and genetic counselling for psychiatric risks in children with rare disorders
Andrew Cuthbert, Aimée Challenger, … Marianne B. M. van den Bree·bioRxiv·Feb 22, 2019
- Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach
Katrina M. Romagnoli, Zachary M. Salvati, … Marc S. Williams·Journal of the American Medical Informatics AssociationPeer-reviewed·Mar 4, 2024