Literature DB >> 29789176

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

Willem Eijzenga1, Eveline de Geus1, Cora M Aalfs2, Fred H Menko3, Rolf H Sijmons4, Hanneke C J M de Haes1, Ellen M A Smets5.   

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 homogeneous sample and address counselees' understanding and recall.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cancer risk; Genetic counseling; Motivational interviewing; Randomized controlled trial; Relatives

Mesh:

Year:  2018        PMID: 29789176     DOI: 10.1016/j.pec.2018.05.009

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  5 in total

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Authors:  Jingsong Zhao; Yue Guan; Colleen M McBride
Journal:  Patient Educ Couns       Date:  2022-03-11

Review 2.  Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review.

Authors:  Alison Luk Young; Aalya Imran; Michael J Spoelma; Rachel Williams; Katherine M Tucker; Jane Halliday; Laura E Forrest; Claire E Wakefield; Phyllis N Butow
Journal:  Eur J Hum Genet       Date:  2022-10-17       Impact factor: 5.351

3.  A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial.

Authors:  Lieke M van den Heuvel; Yvonne M Hoedemaekers; Annette F Baas; J Peter van Tintelen; Ellen M A Smets; Imke Christiaans
Journal:  BMJ Open       Date:  2019-07-09       Impact factor: 2.692

4.  IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results.

Authors:  Deborah Cragun; Jason Beckstead; Meagan Farmer; Gillian Hooker; Marleah Dean; Ellen Matloff; Sonya Reid; Ann Tezak; Anne Weidner; Jennifer G Whisenant; Tuya Pal
Journal:  BMC Cancer       Date:  2021-10-13       Impact factor: 4.430

5.  Usefulness of mobile apps for communication of genetic test results to at-risk family members in a U.S. integrated health system: a qualitative approach from user-testing.

Authors:  Cameron B Haas; Aaron Scrol; Chethan Jujjavarapu; Gail P Jarvik; Nora B Henrikson
Journal:  Health Policy Technol       Date:  2021-04-22       Impact factor: 5.211

  5 in total

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