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. 2019 Jun 27;11(7):1466. doi: 10.3390/nu11071466

Table 2.

Differences in sleep disturbance symptoms, daytime functioning, and psychiatric aspects between control (placebo) and test (alpha-s1 casein hydrolysate (ACH)) phases.

Variables Placebo ACH p-Value
Group Time Group × Time
Pittsburgh Sleep Quality Index
Week 0 10.14 ± 0.42 9.79 ± 0.42
Week 2 8.23 ± 0.42 8.79 ± 0.43
Week 4 8.41 ± 0.42 8.51 ± 0.43 0.668 <0.001 ** 0.211
Insomnia Severity Index
Week 0 12.15 ± 0.73 12.08 ± 0.73
Week 2 9.75 ± 0.73 10.50 ± 0.74
Week 4 9.44 ± 0.73 10.04 ± 0.74 0.406 <0.001 ** 0.523
Epworth Sleepiness Scale
Week 0 6.30 ± 0.58 6.72 ± 0.58
Week 2 6.10 ± 0.58 5.91 ± 0.59
Week 4 6.02 ± 0.58 5.67 ± 0.59 0.920 0.039 0.324
Fatigue Severity Scale
Week 0 31.60 ± 1.64 32.55 ± 1.65
Week 2 31.00 ± 1.65 32.64 ± 1.67
Week 4 30.67 ± 1.65 31.29 ± 1.67 0.276 0.462 0.854
Beck Depression Inventory
Week 0 11.65 ± 1.25 12.37 ± 1.26
Week 2 11.49 ± 1.26 12.28 ± 1.27
Week 4 10.41 ± 1.26 10.79 ± 1.27 0.464 0.008 * 0.912
Beck Anxiety Inventory
Week 0 8.04 ± 1.11 7.71 ± 1.11
Week 2 8.41 ± 1.11 7.72 ± 1.12
Week 4 7.70 ± 1.11 7.09 ± 1.12 0.363 0.362 0.924

Data are least square (LS) mean ± standard error of mean (SEM). p-value, linear mixed-effects model was used to analyze the effects of group, time, and group × time for four weeks. * q-value < 0.05 and ** q-value < 0.01, Storey’s positive false discovery rate (pFDR) was calculated to account for multiple testing.