Abstract

Genetic testing is increasingly part of routine clinical care. However, testing decisions may be characterized by regret as findings also implicate blood relatives. It is not known if genetic testing decisions are affected by the way information is presented (i.e., framing effects). We employed a randomized factorial design to examine framing effects on hypothetical genetic testing scenarios (common, life-threatening disease and rare, life-altering disease). Participants (n = 1012) received one of six decision frames: choice, default (n = 2; opt-in, opt-out), or enhanced choice (n = 3, based on the Theory of Planned Behavior). We compared testing decision, satisfaction, regret, and decision cognitions across decision frames and between scenarios. Participants randomized to ‘choice’ were least likely to opt for genetic testing compared with default and enhanced choice frames (78% vs. 83–91%, p < 0.05). Neither satisfaction nor regret differed across frames. Perceived autonomy (behavioral control) predicted satisfaction (B = 0.085, p < 0.001) while lack of control predicted regret (B = 0.346, p < 0.001). Opting for genetic testing did not differ between disease scenarios (p = 0.23). Results suggest framing can nudge individuals towards opting for genetic testing. These findings have important implications for individual self-determination in the genomic era. Similarities between scenarios with disparate disease trajectories point to possible modular approaches for web-based decisional support.

Highlights

  • We considered that framing could affect decision cognitions—yet no significant differences were observed across frames

  • We observed that default frames as well as enhanced choice frames all increased the likelihood of individuals opting for genetic testing compared with the ‘choice’ frame

  • We found framing genetic testing decisions increases the likelihood of individuals opting for genetic testing

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Summary

Introduction

Genetic testing is no longer solely the domain of specialty clinics and test results are used to guide health behavior, disease management, and reproductive choices. Genetic testing decisions are challenging for patients for numerous reasons [2]. Results are not always definitive (i.e., variants of unknown significance), contributing to prognostic uncertainty. Deciding to have genetic testing spurs a sequence of additional decisions arising from test results that may include preventative efforts such as significant lifestyle changes, risk-reducing surgery (e.g., hereditary breast and ovarian cancer syndrome), or reproductive decisions (e.g., pregnancy termination). Genetic tests are unlike other medical tests because results implicate family members [4]. Family dynamics add to the complexity of testing decisions and may contribute to decisional conflict and regret [5]

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