Comparing cancer genetic counselling using telegenetics with in-person and telephone appointments: Results of a partially randomised patient-preference pilot study.

Telehealth cancer genetics genetic counselling service delivery models telegenetics telemedicine

Journal

Journal of telemedicine and telecare
ISSN: 1758-1109
Titre abrégé: J Telemed Telecare
Pays: England
ID NLM: 9506702

Informations de publication

Date de publication:
14 Jul 2022
Historique:
entrez: 14 7 2022
pubmed: 15 7 2022
medline: 15 7 2022
Statut: aheadofprint

Résumé

Direct-to-patient telegenetics, which uses video conferencing to connect health professionals directly to patients' devices, has been widely adopted during the pandemic. However, limited evidence currently supports its use in cancer genetic counselling. Before the pandemic, we conducted a two-arm partially randomised patient-preference pilot trial to evaluate direct-to-patient telegenetics for patients and genetic counsellors. Patients were randomised to a standard care (telephone/in-person) or direct-to-patient telegenetics appointment. Patients completed questionnaires before, during and after appointments measuring: psychological distress, perceived genetic counsellor empathy, telegenetics satisfaction and technical challenges. Genetic counsellor-reported outcomes -measured using purpose-designed questionnaires- included telegenetics satisfaction, therapeutic alliance and time for assessment. Open-ended patient and genetic counsellor questionnaire responses were synthesised using content analysis. Fifty-six patients and seven genetic counsellors participated. Thirteen patients switched appointment type. No significant differences in distress ( Our results suggest that direct-to-patient telegenetics is a satisfactory service delivery model that does not appear to compromise patient-genetic counsellor relationships or increase patient distress. These findings support direct-to-patient telegenetics use in cancer genetic counselling, although larger trials are needed.

Identifiants

pubmed: 35833346
doi: 10.1177/1357633X221112556
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1357633X221112556

Auteurs

Tina Gonzalez (T)

Prince of Wales Hereditary Cancer Centre, 376195Prince of Wales Hospital, Randwick, NSW, Australia.
Department of Clinical Genetics, 60086Royal North Shore Hospital, St Leonards, NSW, Australia.

Kathy Tucker (K)

Prince of Wales Hereditary Cancer Centre, 376195Prince of Wales Hospital, Randwick, NSW, Australia.
Prince of Wales Clinical School, 7800UNSW Medicine and Health, UNSW Sydney, Kensington, NSW, Australia.

Claire E Wakefield (CE)

School of Women's and Children's Health, 7800UNSW Medicine and Health, 7800UNSW Sydney, Kensington, NSW, Australia.
Kids Cancer Centre, 63623Sydney Children's Hospital, Randwick, NSW, Australia.

Peter Geelan-Small (P)

Stats Central, Mark Wainwright Analytical Centre, 7800UNSW Sydney, Kensington, NSW, Australia.

Stephanie Macmillan (S)

Prince of Wales Clinical School, 7800UNSW Medicine and Health, UNSW Sydney, Kensington, NSW, Australia.

Natalie Taylor (N)

School of Population Health, UNSW Medicine and Health, 7800UNSW Sydney, Kensington, NSW, Australia.

Rachel Williams (R)

Prince of Wales Hereditary Cancer Centre, 376195Prince of Wales Hospital, Randwick, NSW, Australia.
Prince of Wales Clinical School, 7800UNSW Medicine and Health, UNSW Sydney, Kensington, NSW, Australia.

Classifications MeSH