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. Author manuscript; available in PMC: 2012 Apr 5.
Published in final edited form as: J Rural Health. 2009 Fall;25(4):372–377. doi: 10.1111/j.1748-0361.2009.00246.x

Table 1.

Scale Development

Factor Analysis for Identification of Hereditary Cancer Factor Loadings
1. Have you heard about testing for inherited susceptibility to cancer? Dropped
Component 1: Confidence (Cronbach alpha=.87) (1=not at all to 5=extremely)
2. How knowledgeable would you rate yourself in identifying individuals with familial/hereditary cancer syndromes? .85
3. How confident are you in your ability to identify individuals with familial/hereditary cancer syndromes? .82
4. How comfortable would you rate yourself in identifying individuals with familial/hereditary cancer syndromes? .88
Component 2: Importance (Cronbach alpha=.83)
5. How important is it for you to identify individuals with familial/hereditary cancer syndromes? .82
6. How effective is identifying individuals with familial/hereditary cancer syndromes in controlling cancer? .67
7. To what extent do your patients need to be identified if they have a familial/hereditary cancer syndrome? .87
8. To what extent do you feel it is your responsibility to identify individuals with familial/hereditary cancer syndromes? .74
Factor Analysis for Knowledge Items (Cronbach alpha=.91)
1. Approximately 10% of all cancers are hereditary. (True) .74
2. If a woman is positive for a mutation associated with a hereditary cancer syndrome but does not develop cancer, her child may also have that mutation. (True) .55
3. All cancer is the result of changes in genetic material. (True) .90
4. In hereditary non-polyposis colon cancer families, colon cancer tends to occur at an older age in each subsequent generation. (False) .68
5. Individuals with hereditary non-polyposis colon cancer tend to have earlier onset cancers than individuals with familial adenomatous polyposis. (False) .64
6. If an individual has early-onset colon cancer but has no family history, s/he may have hereditary non-polyposis colon cancer. (True) .62
7. Four items were relevant to hereditary breast-ovarian cancer, “Cancers with a strong inherited component can occur in both breasts. (True) .90
8. If a woman inherits a BRCA1 or BRCA2 (hereditary breast-ovarian cancer) mutation from her father, she has the same chance of developing breast or ovarian cancer as if she had inherited the mutation from her mother. (True) .91
9. Even if a woman has a mutation in BRCA1, she may not develop cancer. (True) .86
10. A BRCA1 or BRCA2 mutation is most likely suspected in a woman with breast cancer who has a family history of sarcoma and leukemia. (False) .49