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Table 2 Primary and secondary outcomes at baseline and completion of the study. Between-group analysis was performed

From: A randomized controlled pilot trial to assess the effectiveness of a specially formulated food supplement and pelvic floor muscle training in women with stress-predominant urinary incontinence

 

Control Group (N = 16)

Treatment Group (N = 16)

P-value

UDI-6 score before (mean ± SD)

43 ± 18

45 ± 21

0.77

UDI-6 score after (mean ± SD)

33 ± 26

29 ± 22

0.69

UDI-6 score change (mean ± SD)

-10 ± 31

-16 ± 25

0.58

IIQ-7 score before (mean ± SD)

48 ± 23

50 ± 30

0.76

IIQ-7 score after (mean ± SD)

40 ± 28

30 ± 21

0.31

IIQ-7 score change (mean ± SD)

-8 ± 30

-20 ± 27

0.25

Maximum vaginal squeeze pressure before (cmH2O, mean ± SD)

36 ± 18

30 ± 15

0.27

Maximum vaginal squeeze pressure after (cmH2O)

41 ± 21

45 ± 28

0.71

Change in vaginal squeeze pressure (cmH2O, mean ± SD)

5 ± 12

15 ± 15

0.04

Oxford Scale before (mean ± SD)

2.4 ± 0.8

2.2 ± 0.6

0.51

Oxford Scale after (mean ± SD)

2.9 ± 0.5

2.8 ± 0.5

0.53

Oxford Scale change (mean ± SD)

0.5 ± 0.7

0.6 ± 0.5

0.78

PGI-S score before (mean ± SD)

2.8 ± 0.8

3.1 ± 0.8

0.31

PGI-S score after (mean ± SD)

2.6 ± 0.8

2.3 ± 0.8

0.19

PGI-S score change (mean ± SD)

-0.2 ± 0.9

-0.8 ± 0.8

0.04

PGI-I score (mean ± SD)

2.4 ± 1.0

2.6 ± 0.9

0.61

  1. Urogenital Distress Inventory (UDI-6), Incontinence Impact Questionnaire (IIQ-7), Patient Global Impression of Severity and Improvement question (PGI-S and PGI-I)