Literature DB >> 18618513

Randomized trial of a decision aid for individuals considering genetic testing for hereditary nonpolyposis colorectal cancer risk.

Claire E Wakefield1, Bettina Meiser, Judi Homewood, Robyn Ward, Sheridan O'Donnell, Judy Kirk.   

Abstract

BACKGROUND: Despite the potential benefits of genetic testing for hereditary nonpolyposis colorectal cancer (HNPCC) risk, individuals can find the genetic testing decision-making process complicated and challenging. The goal of the current study was to measure the effectiveness of a tailored decision aid designed specifically to assist individuals to make informed decisions regarding genetic testing for HNPCC risk.
METHODS: In all, 153 individuals were randomized to receive the decision aid or a control pamphlet at the end of their first genetic counseling consultation. Of these, 109 (71.2%) completed the first questionnaire 1 week after consultation, whereas 95 (62.1%) completed the 6-month follow-up questionnaire.
RESULTS: Although the decision aid had no significant effect on postdecisional regret or actual genetic testing decision, the trial results demonstrated that participants who received the decision aid had significantly lower levels of decisional conflict (ie, uncertainty) regarding genetic testing (chi-square(1) = 8.97; P = .003) and were more likely to be classified as having made an informed choice concerning genetic testing (chi-square(1) = 4.37; P = .037) than participants who received a control pamphlet. Also, men who received the decision aid had significantly higher knowledge levels regarding genetic testing compared with men who received the control pamphlet, whereas no such differences were found for women (chi-square(2) = 6.76; P = .034).
CONCLUSIONS: A decision aid for individuals considering genetic testing for HNPCC is an effective intervention to reduce uncertainty and assist individuals to make an informed choice regarding genetic testing for HNPCC after genetic counseling. (c) 2008 American Cancer Society.

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Mesh:

Year:  2008        PMID: 18618513     DOI: 10.1002/cncr.23681

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  22 in total

1.  Preferences regarding targeted education and risk assessment in people with a family history of major depressive disorder.

Authors:  Veronica Quinn; Bettina Meiser; Alex Wilde; Zoe Cousins; Kristine Barlow-Stewart; Philip B Mitchell; Peter R Schofield
Journal:  J Genet Couns       Date:  2014-01-10       Impact factor: 2.537

2.  Facilitating informed decisions regarding microsatellite instability testing among high-risk individuals diagnosed with colorectal cancer.

Authors:  Sharon L Manne; Neal J Meropol; David S Weinberg; Hetal Vig; Zohra Ali-Khan Catts; Cheri Manning; Eric Ross; Kristen Shannon; Daniel C Chung
Journal:  J Clin Oncol       Date:  2010-02-08       Impact factor: 44.544

3.  Does a decision aid for prostate cancer affect different aspects of decisional regret, assessed with new regret scales? A randomized, controlled trial.

Authors:  Julia J van Tol-Geerdink; Jan Willem H Leer; Carl J Wijburg; Inge M van Oort; Henk Vergunst; Emile J van Lin; J Alfred Witjes; Peep F M Stalmeier
Journal:  Health Expect       Date:  2015-05-03       Impact factor: 3.377

4.  The Personal Patient Profile-Prostate decision support for men with localized prostate cancer: a multi-center randomized trial.

Authors:  Donna L Berry; Barbara Halpenny; Fangxin Hong; Seth Wolpin; William B Lober; Kenneth J Russell; William J Ellis; Usha Govindarajulu; Jaclyn Bosco; B Joyce Davison; Gerald Bennett; Martha K Terris; Andrea Barsevick; Daniel W Lin; Claire C Yang; Greg Swanson
Journal:  Urol Oncol       Date:  2011-12-07       Impact factor: 3.498

5.  Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.

Authors:  Anita Y Kinney; Karin M Butler; Marc D Schwartz; Jeanne S Mandelblatt; Kenneth M Boucher; Lisa M Pappas; Amanda Gammon; Wendy Kohlmann; Sandra L Edwards; Antoinette M Stroup; Saundra S Buys; Kristina G Flores; Rebecca A Campo
Journal:  J Natl Cancer Inst       Date:  2014-11-05       Impact factor: 13.506

6.  Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.

Authors:  Kristen Dilzell; Kerry Kingham; Kelly Ormond; Uri Ladabaum
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

7.  A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.

Authors:  Christina G S Palmer; Ariadna Martinez; Michelle Fox; Jin Zhou; Nina Shapiro; Yvonne Sininger; Wayne W Grody; Lisa A Schimmenti
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

8.  Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening.

Authors:  Alice G Ames; Alice Jaques; Obioha C Ukoumunne; Alison D Archibald; Rony E Duncan; Jon Emery; Sylvia A Metcalfe
Journal:  Health Expect       Date:  2012-10-15       Impact factor: 3.377

9.  Assessment of microsatellite instability in colorectal cancer patients from Brazil.

Authors:  Sinara M O Leite; Karina B Gomes; Victor C Pardini; Alessandro C S Ferreira; Vanessa C Oliveira; Geraldo M G Cruz
Journal:  Mol Biol Rep       Date:  2010-01       Impact factor: 2.316

Review 10.  Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.

Authors:  Alison M Elliott
Journal:  Cold Spring Harb Perspect Med       Date:  2020-03-02       Impact factor: 6.915

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