Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
03 Sep 2024
Historique:
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 4 9 2024
Statut: epublish

Résumé

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. 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. This study was approved by Clinical Trials Ontario. Results will be shared through stakeholder workshops, national and international conferences and peer-reviewed journals. NCT06455384.

Identifiants

pubmed: 39231549
pii: bmjopen-2024-090084
doi: 10.1136/bmjopen-2024-090084
doi:

Banques de données

ClinicalTrials.gov
['NCT06455384']

Types de publication

Journal Article Clinical Trial Protocol Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

e090084

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: YB and MC are cofounders of Genetics Adviser.

Auteurs

Guylaine D'Amours (G)

Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Marc Clausen (M)

Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Stephanie Luca (S)

Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.

Emma Reble (E)

Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Rita Kodida (R)

Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Daniel Assamad (D)

Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.

Francois Bernier (F)

Department of Medical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada.

Lauren Chad (L)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.

Gregory Costain (G)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

Irfan Dhalla (I)

Care Experience Institute, Unity Health Toronto, Toronto, Ontario, Canada.
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Hanna Faghfoury (H)

Fred A. Litwin Family Centre in Genetic Medicine, University Health Network, Toronto, Ontario, Canada.
Sinai Health, Toronto, Ontario, Canada.

Jan M Friedman (JM)

Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada.

Stacy Hewson (S)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

Trevor Jamieson (T)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

Josh Silver (J)

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Fred A. Litwin Family Centre in Genetic Medicine, University Health Network, Toronto, Ontario, Canada.

Cheryl Shuman (C)

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

Matthew Osmond (M)

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

June C Carroll (JC)

Department of Family Medicine, Sinai Health, Toronto, Ontario, Canada.
Department of Family and Community Medicine, University of Toronto, Toronto, Ontario, Canada.

Rebekah Jobling (R)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.

Anne-Marie Laberge (AM)

Division of Medical Genetics, CHU Sainte-Justine, Montreal, Québec, Canada.
Department of Pediatrics, Université de Montréal, Montreal, Québec, Canada.

Melyssa Aronson (M)

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Zane Cohen Centre for Digestive Diseases, Sinai Health, Toronto, Ontario, Canada.

Eriskay Liston (E)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

Jordan Lerner-Ellis (J)

Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Christian Marshall (C)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.

Michael Brudno (M)

HPC4Health Consortium, Toronto, Ontario, Canada.

Quynh Pham (Q)

Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Centre for Digital Therapeutics, Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.

Frank Rudzicz (F)

Faculty of Computer Science, Dalhousie University, Halifax, Nova Scotia, Canada.
Vector Institute for Artificial Intelligence, Toronto, Ontario, Canada.

Ronald Cohn (R)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Program in Genetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Muhammad Mamdani (M)

Department of Data Science and Advanced Analytics, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Maureen Smith (M)

Patient Partner, Canadian Organization for Rare Disorders, Toronto, Ontario, Canada.

Serena Shastri-Estrada (S)

Department of Occupational Science and Occupational Therapy, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Genetics Navigator Advisory Board, Toronto, Ontario, Canada.

Emily Seto (E)

Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Centre for Digital Therapeutics, Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.

Kevin Thorpe (K)

Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Wendy Ungar (W)

Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Robin Z Hayeems (RZ)

Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Yvonne Bombard (Y)

Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada yvonne.bombard@utoronto.ca.
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

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