Table 1 displays descriptive data of the study population. Participants were considered athletes if they were a member of a varsity team at LMU. The athletic population included: 13 cross-country runners, 13 rowers, 3 swimmers, 1 soccer player, 2 water polo players, and 1 softball player. The population identified their ethnicities as Caucasians (n = 28), Latinos (n = 5), other (n = 5), Asian/Caucasian (n = 3), Latino/Caucasian (n = 3), African Americans (n = 2), and Asian (n = 1). Mean calcium intakes did not differ by sex nor athletic status, therefore data analysis was completed on the group as a whole. Supplements were defined as protein bars, energy bars, smoothies, meal replacement shakes, protein shakes, multi-vitamins, individual mineral supplements, and fortified juice. Table 2 displays the number of participants who consumed dietary supplements according to data collected from the LMU RAM. None of the control subjects reported consuming supplements, while 23 out of the 33 athletes consumed supplements, contributing approximately 350 mg of calcium to their average daily intake. The mean calcium intake calculated via the LMU RAM for all participants was 935 mg ± 420 mg, while the mean calcium intake quantified via the 3DR was 1085 mg ± 573 mg, which did not differ significantly between methods. This was above the national average intake of 863 mg for men and women of all ages (Wright et al., 2003). In addition, the 3DRs demonstrate our population was consuming more than the adequate intake (AI) set by the IOM for adults, of 1,000 mg per day for calcium (Institute of Medicine, 1997). There were 8 of the 16 men and 13 of the 31 women who consumed less than 100% of the calcium AI for their age. When calculating calcium intake via the LMU RAM without considering supplement use, calcium intake decreased to 763 ± 290 mg per day. The validity of the LMU RAM was assessed by comparing calcium intake values from the LMU RAM and the 3DR (Table 3). A Pearson correlation coefficient was calculated to evaluate the relationship between calcium quantified via the LMU RAM and the calcium derived from the 3DR. A strong positive correlation was found between calcium intake measured with the LMU RAM and 3DRs (r(45) = 0.83, p < 0.01), indicating a significant linear relationship between the two variables. Agreement between the two instruments was good (ICC = 0.76, df = 45, p < 0.01). The Pearson correlation for the RAM when excluding dietary supplements was moderate (r(45) = 0.56, df = 45, p < 0.001). Also, agreement between the instruments was fair (ICC = 0.30, df = 45, p < 0.05) when dietary supplement sources of calcium were not considered. When athletes and non-athletes were examined separately, calcium intake remained strongly correlated between the 3DR and LMU RAM (r(31) = 0.84, p < 0.01 for athletes and r(12) = 0.69, p < 0.01 for non-athletes). Agreement between the two instruments also remained good (ICC = 0.84, df = 31, p < 0.01 for athletes and ICC = 0.69, df = 12, p < 0.01 for non-atheltes). In athletes, the correlation values calculated between the 3DR and the LMU RAM without inclusion of supplements decreased (r(31) = 0.59, p < 0.01) and the ICC value became nonsignificant (ICC = 0.25, df = 31, p > 0.05). Table 4 reports mean calcium intakes, Pearson correlations, and ICC values for participants when separated according to supplement use. A strong positive correlation was found between calcium intake measured with the LMU RAM and 3DRs (r(21) = .82, p < 0.01 for supplement users, and r(22) = 0.78, p < 0.01 for non-supplement users), indicating significant linear relationships between the two variables. Agreement between the two instruments was also good for supplement and non-supplements users. The Pearson correlation for the RAM when excluding dietary supplements was moderate (r(21) = 0.53, df = 45, p < 0.01) while the ICC value became nonsignificant (ICC = 0.05, df = 21, p > 0.05). |