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. 2014 Jun 24;10(5):e293–e298. doi: 10.1200/JOP.2013.001192

Table 3.

Survivors' Preferences for Timing of Information

Information At Diagnosis (%) During Treatment (%) End of Treatment (%) During Follow-Up (%) Diagnosis Through Follow-Up (%) Not Sure (%) Do Not Need (%)
Detailed summary of treatment 29.4 25.9 36.5 15.3 35.3 3.5 7.1
Follow-up plan/appointment schedule 14.1 16.5 35.3 36.5 38.8 1.2 0.0
Monitoring plan scans, blood work 16.5 15.3 37.7 41.2 42.4 0.0 1.2
Adverse effects first 1-2 years 21.2 14.1 34.1 38.8 38.8 2.4 2.4
Late effects > 2 years 17.7 8.2 25.9 48.2 43.5 2.4 3.5
Screening for new cancers 10.6 10.6 29.4 42.4 37.7 2.4 3.5
Strategies for fear of recurrence 9.4 10.6 30.6 34.1 29.4 5.9 14.1
Coping after treatment 7.1 12.9 40.0 27.1 22.4 9.4 21.2
Family adjustment 10.6 14.1 29.4 24.7 25.9 10.6 25.9
Support groups 10.6 9.4 25.9 20.0 21.2 11.8 24.7
Pain symptom management 23.5 21.2 14.1 12.9 38.8 0.0 28.2
Integrative medicine 22.4 9.4 14.1 10.6 30.6 8.3 22.4
Nutrition 22.4 18.8 15.3 15.3 47.1 1.2 12.9
Exercise 18.8 16.5 14.1 14.1 45.9 3.5 14.1
Genetic counseling 15.3 1.2 8.2 15.3 14.1 16.5 32.9
Fertility 22.4 4.7 7.1 10.6 5.9 5.9 50.6
Sexual health 20.0 11.8 14.1 17.7 22.4 4.7 35.3
Smoking cessation 9.4 3.5 5.9 3.5 14.1 9.4 54.1
Financial resources 23.5 3.5 5.9 7.1 25.9 8.3 34.1
Vocational employment counseling 8.2 3.5 9.4 11.8 14.1 10.6 49.4
Resources around health insurance 25.9 3.5 8.2 5.9 25.9 8.2 31.8

NOTE. Boldface indicates most commonly reported timing for the information, or information items “not needed.”