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Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention

BACKGROUND: Genetic information given to an individual newly diagnosed with a genetic condition is likely to have important health implications for other family members. The task of communicating with these relatives commonly falls to the newly diagnosed person. Talking to relatives about genetic in...

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Autores principales: Hodgson, Jan M, Metcalfe, Sylvia A, Aitken, MaryAnne, Donath, Susan M, Gaff, Clara L, Winship, Ingrid M, Delatycki, Martin B, Skene, Loane LC, McClaren, Belinda J, Paul, Jean L, Halliday, Jane L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995589/
https://www.ncbi.nlm.nih.gov/pubmed/24628824
http://dx.doi.org/10.1186/1471-2350-15-33
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author Hodgson, Jan M
Metcalfe, Sylvia A
Aitken, MaryAnne
Donath, Susan M
Gaff, Clara L
Winship, Ingrid M
Delatycki, Martin B
Skene, Loane LC
McClaren, Belinda J
Paul, Jean L
Halliday, Jane L
author_facet Hodgson, Jan M
Metcalfe, Sylvia A
Aitken, MaryAnne
Donath, Susan M
Gaff, Clara L
Winship, Ingrid M
Delatycki, Martin B
Skene, Loane LC
McClaren, Belinda J
Paul, Jean L
Halliday, Jane L
author_sort Hodgson, Jan M
collection PubMed
description BACKGROUND: Genetic information given to an individual newly diagnosed with a genetic condition is likely to have important health implications for other family members. The task of communicating with these relatives commonly falls to the newly diagnosed person. Talking to relatives about genetic information can be challenging and is influenced by many factors including family dynamics. Research shows that many relatives remain unaware of relevant genetic information and the possible impact on their own health. This study aims to evaluate whether a specific genetic counselling intervention for people newly diagnosed with a genetic condition, implemented over the telephone on a number of occasions, could increase the number of at-risk relatives who make contact with genetics services after a new genetic diagnosis within a family. METHODS: This is a prospective, multi-centre randomised controlled trial being conducted at genetics clinics at five public hospitals in Victoria, Australia. A complex genetic counselling intervention has been developed specifically for this trial. Probands (the first person in a family to present with a diagnosis of a genetic condition) are being recruited and randomised into one of two arms – the telephone genetic counselling intervention arm and the control arm receiving usual care. The number of at-risk relatives for each proband will be estimated from a family pedigree collected at the time of diagnosis. The primary outcome will be measured by comparing the proportion of at-risk relatives in each arm of the trial who make subsequent contact with genetics services. DISCUSSION: This study, the first randomised controlled trial of a complex genetic counselling intervention to enhance family communication, will provide evidence about how best to assist probands to communicate important new genetic information to their at-risk relatives. This will inform genetic counselling practice in the context of future genomic testing. TRIAL REGISTRATION: Australia and New Zealand Clinical Trials Register (ANZCTR): ANZCTRN12608000642381.
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spelling pubmed-39955892014-04-23 Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention Hodgson, Jan M Metcalfe, Sylvia A Aitken, MaryAnne Donath, Susan M Gaff, Clara L Winship, Ingrid M Delatycki, Martin B Skene, Loane LC McClaren, Belinda J Paul, Jean L Halliday, Jane L BMC Med Genet Study Protocol BACKGROUND: Genetic information given to an individual newly diagnosed with a genetic condition is likely to have important health implications for other family members. The task of communicating with these relatives commonly falls to the newly diagnosed person. Talking to relatives about genetic information can be challenging and is influenced by many factors including family dynamics. Research shows that many relatives remain unaware of relevant genetic information and the possible impact on their own health. This study aims to evaluate whether a specific genetic counselling intervention for people newly diagnosed with a genetic condition, implemented over the telephone on a number of occasions, could increase the number of at-risk relatives who make contact with genetics services after a new genetic diagnosis within a family. METHODS: This is a prospective, multi-centre randomised controlled trial being conducted at genetics clinics at five public hospitals in Victoria, Australia. A complex genetic counselling intervention has been developed specifically for this trial. Probands (the first person in a family to present with a diagnosis of a genetic condition) are being recruited and randomised into one of two arms – the telephone genetic counselling intervention arm and the control arm receiving usual care. The number of at-risk relatives for each proband will be estimated from a family pedigree collected at the time of diagnosis. The primary outcome will be measured by comparing the proportion of at-risk relatives in each arm of the trial who make subsequent contact with genetics services. DISCUSSION: This study, the first randomised controlled trial of a complex genetic counselling intervention to enhance family communication, will provide evidence about how best to assist probands to communicate important new genetic information to their at-risk relatives. This will inform genetic counselling practice in the context of future genomic testing. TRIAL REGISTRATION: Australia and New Zealand Clinical Trials Register (ANZCTR): ANZCTRN12608000642381. BioMed Central 2014-03-14 /pmc/articles/PMC3995589/ /pubmed/24628824 http://dx.doi.org/10.1186/1471-2350-15-33 Text en Copyright © 2014 Hodgson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Hodgson, Jan M
Metcalfe, Sylvia A
Aitken, MaryAnne
Donath, Susan M
Gaff, Clara L
Winship, Ingrid M
Delatycki, Martin B
Skene, Loane LC
McClaren, Belinda J
Paul, Jean L
Halliday, Jane L
Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title_full Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title_fullStr Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title_full_unstemmed Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title_short Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
title_sort improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995589/
https://www.ncbi.nlm.nih.gov/pubmed/24628824
http://dx.doi.org/10.1186/1471-2350-15-33
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