Perceived importance of genome sequencing |
Mean (SD) |
3.76 (0.55) |
|
|
|
Range |
1.4–5.0 |
|
|
|
Knowledge of genomics |
Mean (SD) |
0.47 (0.24) |
|
|
|
Range |
0–1 |
|
|
|
Perceived ability to cope with genome sequencing results |
Mean (SD) |
4.17 (0.67) |
|
|
|
Range |
1–5 |
|
|
|
Intention to change behavior if gene variant indicating cancer risk was found |
Mean (SD) |
4.25 (0.66) |
|
|
|
Range |
1–5 |
|
|
|
Attitude towards uncertainty |
Mean (SD) |
4.03 (0.68) |
|
|
|
Range |
1.57–5 |
|
|
|
Fear of cancer recurrence |
Mean (SD) |
13.76 (815) |
12.36 (7.94) |
11.89 (8.15) |
F(1.90, 494.21)=10.26, p = 0.000 |
Range |
0–30 |
0–30 |
0–30 |
|
Perceived susceptibility of (another) cancer |
Mean (SD) |
64.78 (16.44) |
65.09 (16.33) |
65.87 (17.82) |
F(1.94, 503.19) = 0.69, p = 0.500 |
Satisfaction with decision to have genome sequencing |
Mean (SD) |
26.17 (3.17) |
26.74 (3.89) |
26.33 (4.13) |
F(1.93, 494.50)=2.33, p = 0.100 |
Genome sequencing anxiety |
Mean (SD) |
|
5.78 (9.94) |
6.38 (11.82) |
t(265) = −1.160, p = 0.247 |
General anxiety and depressive symptoms |
Mean (SD) |
|
7.98 (6.66) |
8.53 (7.30) |
t(265)=-1.610, p = 0.109 |
Anxiety subscale
|
|
Mean (SD) |
|
5.15 (4.09) |
5.48 (4.44) |
t(265)= −1.617, p = 0.107 |
Depression subscale
|
|
Mean (SD) |
|
2.83 (3.25) |
3.04 (3.45) |
t(265) = −1.205, p = 0.229 |
Hope |
Mean (SD) |
|
39.30 (5.52) |
39.23 (6.07) |
t(211) = 0.203, p = 0.839 |
Distress |
Mean (SD) |
|
22.34 (9.49) |
23.20 (10.29) |
t(210) = −1.354, p = 0.177 |
Perceived uncertainty about genome sequencing |
Mean (SD) |
|
8.23 (7.37) |
7.95 (7.64) |
t(210) = 0.660, p=0.510 |