Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations
Trevor Jamieson,
Kevin Thorpe,
Francois Bernier,
Melyssa Aronson,
Marc Clausen,
Rita Kodida,
Emma Reble,
June C Carroll,
Jordan Lerner-Ellis,
Yvonne Bombard,
Matthew Osmond,
Muhammad Mamdani,
Ronald Cohn,
Emily Seto,
Hanna Faghfoury,
Josh Silver,
Maureen Smith,
Lauren Chad,
Jan M Friedman,
Robin Z Hayeems,
Michael Brudno,
Gregory Costain,
Quynh Pham,
Anne-Marie Laberge,
Christian Marshall,
Cheryl Shuman,
Rebekah Jobling,
Irfan Dhalla,
Serena Shastri-Estrada,
Daniel Assamad,
Stephanie Luca,
Stacy Hewson,
Eriskay Liston,
Frank Rudzicz,
Wendy Ungar,
Guylaine D'Amours
Affiliations
Trevor Jamieson
Department of Medicine, University of Toronto, Toronto, Ontario, Canada
Kevin Thorpe
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada
Francois Bernier
Department of Medical Genetics, Alberta Children`s Hospital, Calgary, Alberta, Canada
Melyssa Aronson
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
Marc Clausen
Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
Rita Kodida
Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
Emma Reble
Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
June C Carroll
Department of Family Medicine, Sinai Health, Toronto, Ontario, Canada
Jordan Lerner-Ellis
Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada
Yvonne Bombard
Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
Matthew Osmond
Children`s Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada
Muhammad Mamdani
Department of Data Science and Advanced Analytics, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
Ronald Cohn
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Emily Seto
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada
Hanna Faghfoury
Fred A. Litwin Family Centre in Genetic Medicine, University Health Network, Toronto, Ontario, Canada
Josh Silver
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
Maureen Smith
Patient Partner, Canadian Organization for Rare Disorders, Toronto, Ontario, Canada
Lauren Chad
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Jan M Friedman
Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada
Robin Z Hayeems
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada
Michael Brudno
HPC4Health Consortium, Toronto, Ontario, Canada
Gregory Costain
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Quynh Pham
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada
Anne-Marie Laberge
Division of Medical Genetics, CHU Sainte-Justine, Montreal, Québec, Canada
Christian Marshall
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada
Cheryl Shuman
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
Rebekah Jobling
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Irfan Dhalla
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada
Serena Shastri-Estrada
Department of Occupational Science and Occupational Therapy, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
Daniel Assamad
Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada
Stephanie Luca
Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada
Stacy Hewson
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Eriskay Liston
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada
Frank Rudzicz
Faculty of Computer Science, Dalhousie University, Halifax, Nova Scotia, Canada
Wendy Ungar
Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada
Guylaine D'Amours
Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada
Introduction Genetic testing is used across medical disciplines leading to unprecedented demand for genetic services. This has resulted in excessive waitlists and unsustainable pressure on the standard model of genetic healthcare. Alternative models are needed; e-health tools represent scalable and evidence-based solution. We aim to evaluate the effectiveness of the Genetics Navigator, an interactive patient-centred digital platform that supports the collection of medical and family history, provision of pregenetic and postgenetic counselling and return of genetic testing results across paediatric and adult settings.Methods and analysis We will evaluate the effectiveness of the Genetics Navigator combined with usual care by a genetics clinician (physician or counsellor) to usual care alone in a randomised controlled trial. One hundred and thirty participants (adults patients or parents of paediatric patients) eligible for genetic testing through standard of care will be recruited across Ontario genetics clinics. Participants randomised into the intervention arm will use the Genetics Navigator for pretest and post-test genetic counselling and results disclosure in conjunction with their clinician. Participants randomised into the control arm will receive usual care, that is, clinician-delivered pretest and post-test genetic counselling, and results disclosure. The primary outcome is participant distress 2 weeks after test results disclosure. Secondary outcomes include knowledge, decisional conflict, anxiety, empowerment, quality of life, satisfaction, acceptability, digital health literacy and health resource use. Quantitative data will be analysed using statistical hypothesis tests and regression models. A subset of participants will be interviewed to explore user experience; data will be analysed using interpretive description. A cost-effectiveness analysis will examine the incremental cost of the Navigator compared with usual care per unit reduction in distress or unit improvement in quality of life from public payer and societal perspectives.Ethics and dissemination This study was approved by Clinical Trials Ontario. Results will be shared through stakeholder workshops, national and international conferences and peer-reviewed journals.Trial registration number NCT06455384.