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Table 3 Percentage of CML patients who perceived to receive no or little information per item of the EORTC QLQ-INFO25 and mean scores (SD) on information provision scales of the EORTC QLQ-INFO25, questionnaire vs intervention group

From: Effectiveness of digital care platform CMyLife for patients with chronic myeloid leukemia: results of a patient-preference trial

 

Questionnaire group

Intervention group

 

Percentage of cml patients who perceived to receive no or little information about:

Pre (n = 33) %

Post (n = 29) %

Δ

Pre (n = 75) %

Post (n = 57) %

Δ

Corrected P-value

The diagnosis of your disease

30.3

31.0

0.7

26.4

17.9

−8.5

.248

The extent (spread) of your disease

42.4

55.2

12.8

41.9

33.9

−8

.133

The possible causes of your disease

68.8

65.5

−3.3

64.9

55.4

−9.5

.505

Whether the disease is under control

18.2

17.2

−1

17.6

12.5

−5.1

.281

The purpose of any medical tests you have had or may undergo

27.3

31.0

3.7

20.3

16.1

−4.2

.448

The procedures of the medical tests

24.2

24.1

−0.1

23.0

16.4

−6.6

.608

The results of the medical tests you have already received

18.2

10.3

−7.9

12.2

9.1

−3.1

.622

The medical treatment

18.2

13.8

−4.4

13.5

9.1

− 4.4

.391

The expected benefit of the treatment

30.2

27.6

−2.6

18.9

9.1

−9.8

.106

The possible side-effects of your treatment

54.5

35.7

−18.8

51.4

27.3

−24.1

.688

The expected effects of the treatment on disease symptoms

48.5

34.5

−14

41.9

27.3

−14.6

.877

The effects of the treatment on social and family life

87.9

72.4

−15.5

81.1

72.7

−8.4

.529

The effect of the treatment on sexual activity

83.9

82.8

−1.1

90.5

88.9

−1.6

.940

Additional help outside the hospital

90.9

93.1

2.2

97.2

85.5

−11.7

.025

Rehabilitation services

90.9

92.9

2

94.5

87.3

−7.2

.155

Aspects of managing your illness at home

93.9

86.2

−7.7

87.7

85.5

−2.2

.357

Possible professional psychological support

93.8

96.6

2.8

84.9

78.6

−6.3

.163

Different locations of care

84.4

93.1

8.7

89.0

85.5

−3.5

.155

Things that you can do to help yourself get well

75.0

78.6

3.6

78.1

78.2

0.1

.402

EORTC-QLQ-INFO25 scalesa

Questionnaire group

Intervention group

 
 

Pre (n = 33)

Mean (SD)

Post (n = 29)

Mean (SD)

Δ

Pre (n = 75)

Mean (SD)

Post (n = 57)

Mean (SD)

Δ

Corrected P-value

Information about

 Disease

58.8 (24.1)

57.2 (22.5)

−1.6

57.1 (21.1)

63.2 (20.6)

6.1

.115

 Medical tests

71.7 (24.2)

67.8 (20.6)

−3.9

69.7 (22.5)

70.0 (22.2)

0.3

.442

 Treatments

48.1 (18.4)

53.8 (21.7)

5.7

50.2 (19.1)

55.4 (18.1)

5.2

.854

 Other services

12.4 (18.1)

13.2 (19.7)

0.8

16.4 (18.6)

22.3 (25.6)

5.9

.252

 Different location of care facilities

18.7 (25.3)

10.3 (20.1)

−8.4

16.9 (24.3)

20.0 (30.5)

3.1

.052

 How to help yourself

29.2 (31.4)

29.8 (30.5)

0.6

30.6 (26.5)

33.3 (30.1)

2.7

.513

Received written information

68.8 (47.1)

67.9 (47.6)

−0.9

70.3 (46.0)

71.4 (45.6)

1.1

.884

Received cd/video

6.06 (24.2)

10.3 (31.0)

4.24

5.48 (22.9)

7.14 (26.0)

1.66

.538

Satisfaction with amount of information

43.4 (25.7)

41.4 (21.2)

−2

38.4 (23.4)

36.4 (20.6)

−2

.865

Wish to receive more info

33.3 (47.9)

31.0 (47.1)

−2.3

45.9 (50.2)

22.8 (42.3)

−23.1

.106

Wish to receive less info

66.7 (47.9)

69.0 (47.1)

2.3

54.1 (50.2)

77.8 (42.0)

23.7

.105

Helpfulness of information

31.3 (26.3)

34.5 (26.4)

3.2

31.1 (21.8)

32.1 (22.2)

1

.222

Global score

46.3 (16.1)

46.7 (17.0)

0.4

47.1 (15.9)

51.2 (16.5)

4.1

.161

  1. P-value shows the difference between intervention and questionnaire with regard to the within-subject change between baseline and post-measurement
  2. Δ = difference between pre- and post-measurements
  3. aScores between 0 and 100, higher scores indicate more/better information and satisfaction