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. 2011 Sep 18;27(3):297–306. doi: 10.1007/s00455-011-9366-9

Table 3.

Means (and 95% confidence intervals) for 24-h fluid intake measures at baseline and at the post-trial measurement

Time point Parameter Control phase Water protocol
No oral water access (N = 7) Unsupervised oral water access (N = 6) Supervised oral water access (N = 9) Access conditions combined (N = 15)
Pre-trial fluid balance Oral water intake (cc) N/A N/A N/A N/A
Other fluid intake (cc) 1474 (1113–1836) 1407 (729–2086) 1495 (1167–1823) 1460 (1180–1740)
Total fluid intake (cc) 1474 (1113–1836) 1407 (729–2086) 1495 (1167–1823) 1460 (1180–1740)
% of calculated requirements (%) 63 (48–78) 65 (30–100) 68 (53–82) 67 (53–81)
Post-trial fluid balance Oral water intake (cc) N/A 920 (181–1658) 326 (43–609) 563 (238–888)
Other fluid intake (cc) 1427 (999–1855) 1039 (682–1396) 1423 (1009–1876) 1281 (996–1566)
Total fluid intake (cc) 1427 (999–1855) 1959 (1172–2745) 1768 (1397–2140) 1845 (1520–2169)
% of calculated requirements (%) 61 (44–79) 90 (49–130) 80 (64–96) 84 (69–100)

Fluid: liquid consistency at room temperature. Total fluid intake: the combination of oral water intake plus other fluid intake (including oral thickened liquids and nonoral fluids)