This study assessed the extent to which different formats of informing men
and women age 50 and over of the risks of colorectal cancer (CRC) affected
their perceptions of their absolute and comparative (self versus other) 10-
year and lifetime risks; emotional reactions about getting CRC; and screeni
ng intentions. Forty-four men and 78 women received information about the a
bsolute lifetime risk of getting CRC. In addition, participants either did
or did not receive information about (1) lifetime risk of getting CRC compa
red with other cancers, and (2) risk factors for CRC (age and polyps). Part
icipants who received risk factors information were more likely to increase
their perceived absolute 10-year and lifetime risks of getting CRC compare
d with participants who did not receive risk factors information. In additi
on, participants who received risk factors information were more likely to
believe age was related to getting CRC and felt at greater risk for having
polyps compared with participants who did not receive this information. Non
e of the experimental conditions affected how worried anxious, and fearful
participants felt about getting CRC, nor did they affect screening intentio
ns. Independent of experimental condition, participants tended to increase
their intentions to get screened for CRC in the next year or two. Intention
to be screened was more pronounced among participants who had been screene
d via a fecal occult blood test (FOBT) or sigmoidoscopy (SIG). Implications
for the design of interventions involving the communication of CRC risks a
re discussed.