Table 2.

Proposed psychosocial measures

1. Numeracy and perceived risk

2. Attitude towards genetic testing

3. Genetic knowledge and understanding of genetic risk

4. Reaction to risk results and rating of test results information

5. Genetic counseling satisfaction and perceived personal control

6. Shared decision-making and physician visit satisfaction

7. Intention to change

8. Information sharing

9. Recall and decisional regret

10. Anxiety and impact of events