How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial (2024)

Abstract

Objective: In hereditary and familial cancer, counselees are requested to inform their at-risk relatives. We developed an intervention to support counselees in this task. Methods: A randomized controlled trial was conducted aimed at improving cancer genetic counselees’ i) knowledge, ii) motivation to disclose information, and ii) self-efficacy in this regard. Eligible participants were randomized to telephonic counseling (n = 148), or standard care (n = 157) and assessed at baseline, 1 week post-intervention, and 4 months after study enrolment. Results: No between-group differences were found in participants’ knowledge, motivation, and self-efficacy. Knowledge concerning which second-degree relatives to inform was lower compared to first-degree relatives. About 60% of the participants was of the opinion that they needed to inform more relatives than stated in their summary letter and only about 50% were correctly aware of which information to disclose. Of note, at baseline, almost 80% of the participants had already correctly informed their at-risk relatives. Conclusions: Since, unexpectedly, counselees already informed most of their relatives before the intervention was offered, efficacy of the intervention could not convincingly be determined. Counselees’ knowledge about whom to inform about what is suboptimal. Practice Implications: Future interventions should target a more hom*ogeneous sample and address counselees’ understanding and recall.

Original languageEnglish
Pages (from-to)1611-1619
JournalPatient Education and Counseling
Volume101
Issue number9
DOIs
Publication statusPublished - 2018

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Eijzenga, W., de Geus, E., Aalfs, C. M., Menko, F. H., Sijmons, R. H., de Haes, H. C. J. M. (2018). How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial. Patient Education and Counseling, 101(9), 1611-1619. https://doi.org/10.1016/j.pec.2018.05.009

Eijzenga, Willem ; de Geus, Eveline ; Aalfs, Cora M. et al. / How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial. In: Patient Education and Counseling. 2018 ; Vol. 101, No. 9. pp. 1611-1619.

@article{a187ecebb9644f64a14b707f480393e0,

title = "How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial",

abstract = "Objective: In hereditary and familial cancer, counselees are requested to inform their at-risk relatives. We developed an intervention to support counselees in this task. Methods: A randomized controlled trial was conducted aimed at improving cancer genetic counselees{\textquoteright} i) knowledge, ii) motivation to disclose information, and ii) self-efficacy in this regard. Eligible participants were randomized to telephonic counseling (n = 148), or standard care (n = 157) and assessed at baseline, 1 week post-intervention, and 4 months after study enrolment. Results: No between-group differences were found in participants{\textquoteright} knowledge, motivation, and self-efficacy. Knowledge concerning which second-degree relatives to inform was lower compared to first-degree relatives. About 60% of the participants was of the opinion that they needed to inform more relatives than stated in their summary letter and only about 50% were correctly aware of which information to disclose. Of note, at baseline, almost 80% of the participants had already correctly informed their at-risk relatives. Conclusions: Since, unexpectedly, counselees already informed most of their relatives before the intervention was offered, efficacy of the intervention could not convincingly be determined. Counselees{\textquoteright} knowledge about whom to inform about what is suboptimal. Practice Implications: Future interventions should target a more hom*ogeneous sample and address counselees{\textquoteright} understanding and recall.",

author = "Willem Eijzenga and {de Geus}, Eveline and Aalfs, {Cora M.} and Menko, {Fred H.} and Sijmons, {Rolf H.} and {de Haes}, {Hanneke C. J. M.} and Smets, {Ellen M. A.}",

year = "2018",

doi = "https://doi.org/10.1016/j.pec.2018.05.009",

language = "English",

volume = "101",

pages = "1611--1619",

journal = "Patient Education and Counseling",

issn = "0738-3991",

publisher = "Elsevier Ireland Ltd",

number = "9",

}

Eijzenga, W, de Geus, E, Aalfs, CM, Menko, FH, Sijmons, RH, de Haes, HCJM 2018, 'How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial', Patient Education and Counseling, vol. 101, no. 9, pp. 1611-1619. https://doi.org/10.1016/j.pec.2018.05.009

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial. / Eijzenga, Willem; de Geus, Eveline; Aalfs, Cora M. et al.
In: Patient Education and Counseling, Vol. 101, No. 9, 2018, p. 1611-1619.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial

AU - Eijzenga, Willem

AU - de Geus, Eveline

AU - Aalfs, Cora M.

AU - Menko, Fred H.

AU - Sijmons, Rolf H.

AU - de Haes, Hanneke C. J. M.

AU - Smets, Ellen M. A.

PY - 2018

Y1 - 2018

N2 - Objective: In hereditary and familial cancer, counselees are requested to inform their at-risk relatives. We developed an intervention to support counselees in this task. Methods: A randomized controlled trial was conducted aimed at improving cancer genetic counselees’ i) knowledge, ii) motivation to disclose information, and ii) self-efficacy in this regard. Eligible participants were randomized to telephonic counseling (n = 148), or standard care (n = 157) and assessed at baseline, 1 week post-intervention, and 4 months after study enrolment. Results: No between-group differences were found in participants’ knowledge, motivation, and self-efficacy. Knowledge concerning which second-degree relatives to inform was lower compared to first-degree relatives. About 60% of the participants was of the opinion that they needed to inform more relatives than stated in their summary letter and only about 50% were correctly aware of which information to disclose. Of note, at baseline, almost 80% of the participants had already correctly informed their at-risk relatives. Conclusions: Since, unexpectedly, counselees already informed most of their relatives before the intervention was offered, efficacy of the intervention could not convincingly be determined. Counselees’ knowledge about whom to inform about what is suboptimal. Practice Implications: Future interventions should target a more hom*ogeneous sample and address counselees’ understanding and recall.

AB - Objective: In hereditary and familial cancer, counselees are requested to inform their at-risk relatives. We developed an intervention to support counselees in this task. Methods: A randomized controlled trial was conducted aimed at improving cancer genetic counselees’ i) knowledge, ii) motivation to disclose information, and ii) self-efficacy in this regard. Eligible participants were randomized to telephonic counseling (n = 148), or standard care (n = 157) and assessed at baseline, 1 week post-intervention, and 4 months after study enrolment. Results: No between-group differences were found in participants’ knowledge, motivation, and self-efficacy. Knowledge concerning which second-degree relatives to inform was lower compared to first-degree relatives. About 60% of the participants was of the opinion that they needed to inform more relatives than stated in their summary letter and only about 50% were correctly aware of which information to disclose. Of note, at baseline, almost 80% of the participants had already correctly informed their at-risk relatives. Conclusions: Since, unexpectedly, counselees already informed most of their relatives before the intervention was offered, efficacy of the intervention could not convincingly be determined. Counselees’ knowledge about whom to inform about what is suboptimal. Practice Implications: Future interventions should target a more hom*ogeneous sample and address counselees’ understanding and recall.

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UR - https://www.ncbi.nlm.nih.gov/pubmed/29789176

U2 - https://doi.org/10.1016/j.pec.2018.05.009

DO - https://doi.org/10.1016/j.pec.2018.05.009

M3 - Article

C2 - 29789176

SN - 0738-3991

VL - 101

SP - 1611

EP - 1619

JO - Patient Education and Counseling

JF - Patient Education and Counseling

IS - 9

ER -

Eijzenga W, de Geus E, Aalfs CM, Menko FH, Sijmons RH, de Haes HCJM et al. How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial. Patient Education and Counseling. 2018;101(9):1611-1619. doi: https://doi.org/10.1016/j.pec.2018.05.009

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial (2024)

FAQs

What is genetic counseling for hereditary cancer risk? ›

Genetic counseling is helpful for individuals with more than one family member with the same or related types of cancer (e.g. breast and ovarian cancer or colon and uterine cancer), personal and/or family history of early-onset cancer, personal and/or family history of rare cancers (e.g. male breast cancer or fallopian ...

What is the role of genetic counseling in cancer? ›

It could also provide useful information for your family members about their cancer risks. A genetic counselor can also refer you to support resources for people with cancer, an increased chance of cancer, or family histories of cancer.

What is the role of genetic Counselling in preventing hereditary disease? ›

Genetic counselors help identify families at possible risk of a genetic condition by gathering and analyzing family history and inheritance patterns and calculating chances of recurrence.

How does genetic counseling help families? ›

They help to identify families at possible risk of a genetic disorder, gather and analyze family history and inheritance patterns, calculate risks of recurrence, and provide information about genetic testing and related procedures.

What is the most important responsibility of a genetic counselor? ›

Genetic counselors assess clients' risk for a variety of inherited conditions, such as birth defects. They review genetic test results with individuals and families and support them in making decisions based on those results. They also offer information to other healthcare providers.

What does genetic counseling typically involve? ›

In a typical day, genetic counselors: Determine risk for certain diseases or disorders. Analyze family health history to look for inherited health risks. Educate individuals regarding their chance for inheriting genetic diseases.

How can genetic Counselling help? ›

Genetic counselling can help you: understand more about a genetic condition and what causes it. understand the risk of you or your family member having a genetic condition. work out whether to have genetic testing.

What is gene therapy for hereditary cancer? ›

Gene transfer is a new treatment modality that introduces new genes into a cancerous cell or the surrounding tissue to cause cell death or slow the growth of the cancer. This treatment technique is very flexible, and a wide range of genes and vectors are being used in clinical trials with successful outcomes.

What is genetic counseling in genetics? ›

Genetic counseling gives you information about how genetic conditions might affect you or your family. The genetic counselor or other healthcare professional will collect your personal and family health history.

Why would I be referred to genetic counseling? ›

The reasons that a person might be referred to a genetic counselor, medical geneticist, or other genetics professional include: A personal or family history of a genetic condition, birth defect, chromosomal disorder, or hereditary cancer. Two or more pregnancy losses (miscarriages), a stillbirth, or a baby who died.

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