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. 2016 Jun 18;24(11):4639–4649. doi: 10.1007/s00520-016-3307-y

Table 3.

Floor and ceiling effects of the SCNS-SF34 and suggested factor structure in head and neck cancer patients (n = 201)

Item Factor loadings1
Lowest score (%) Highest score (%) 1 2 3 4
Physical and daily living 38.8 0
 1. Pain 70.9 2.5 .39 .54
 2. Lack of energy/tiredness 51.0 4.5 .33 .51 .60
 3. Feelings unwell a lot of the time 74.6 1.0 .53 .67
 4. Work around the home 58.4 3.0 .76
 5. Not being able to do the things you used to do 57.7 7.5 .39 .39 .69
Psychological 29.7 0
 6. Anxiety 68.0 2.5 .78 .31
 7. Feeling down or depressed 67.7 1.0 .32 .78
 8. Feelings of sadness 66.7 2.0 .81
 9. Fears about the cancer spreading 51.5 8.5 .85
 10. Worry that the results of treatment are beyond your control 59.7 3.5 .34 .74
 11. Uncertainty about the future 50.0 5.5 .33 .82
 12. Learning to feel in control of your situation 58.0 1.5 .35 .68 .41
 13. Keeping a positive look 54.2 3.5 .31 .52 .42
 14. Feelings about death and dying 65.0 4.5 .79
 17. Concerns about the worries of those close to you 60.5 2.5 .38 .42 .30
Sexuality 69.9 .5
 15. Changes in sexual feelings 75.3 3.0 .48 .74
 16. Changes in your sexual relationships 77.8 2.5 .36 .84
 31. To be given information about sexual relationships 85.4 .5 .76
Health system, information and patient support 21.1 0
 18. More choice about which cancer specialists you see 67.5 1.5 .47 .41
 20. Reassurance by medical staff that the way you feel is normal 43.5 2.5 .62 .34 .31
 21. Hospital staff attending promptly to your physical needs 57.5 2.0 .73
 22. Hospital staff acknowledging, and showing sensitivity to your feelings and emotional needs 55.0 1.5 .75
 23. Being given written information about the important aspects of your care 58.0 2.0 .75
 24. Being given information (written, diagrams, drawings) about aspects of managing your illness and side effects at home 61.5 4.0 .65 .30
 25. Being given explanations of those tests for which you would like explanations 46.2 2.5 .72 .31
 26. Being adequately informed about the benefits and side effects of treatments before you choose to have them 47.2 4.5 .79
 27. Being informed about your test results as soon as feasible 43.3 11.9 .74 .31
 28. Being informed about cancer which is under control or diminishing (that is, remission) 38.3 10.4 .77 .37
 29. Being informed about things you can do to help yourself to get well 50.2 8.5 .78 .30
 30. Having access to professional counselling (e.g. psychologist, social worker, counsellor, nurse specialist) if you, your family or friends need it 66.7 4.5 .67 .35
 32. Being treated like a person not just another case 53.2 9.5 .79
 33. Being treated in a hospital or clinic that is as physically pleasant as possible 44.3 6.5 .72
 34. Having one member of hospital staff with whom you can talk to about all aspects of your condition, treatment and follow-up 47.3 6.5 .78
 19. More choice about which hospital you attend 68.5 2.0
Eigenvalue 16.69 3.34 1.67 1.23
Variance 50.58 10.11 5.05 3.71
Cronbach’s α .95 .95 .89 .79

aLoadings >.3 are presented, and main (i.e. highest) loading is italicized