<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Boer IH</submitter><funding>NCATS NIH HHS</funding><funding>NHLBI</funding><funding>NIDDK NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>106318</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8089051</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>103</volume><pubmed_abstract>The INdividual response to VITamin D (INVITe) trial was a randomized, placebo-controlled, parallel group trial of vitamin D&lt;sub>3&lt;/sub> supplementation (2000 IU daily) designed to determine clinical and genetic characteristics that modify the response to vitamin D supplementation. To enhance internal and external validity and reduce cost, the INVITe trial was nested within the Multi-Ethnic Study of Atherosclerosis (MESA), an ongoing prospective observational cohort study. The INVITe trial enrolled a community-based population of 666 racially and ethnically diverse participants from January 2017 to April 2019. This represents 30% of 2210 MESA participants approached for screening, and 96% of those found to be eligible. Barriers to enrollment included delayed initiation of the trial relative</pubmed_abstract><journal>Contemporary clinical trials</journal><pubmed_title>The Multi-Ethnic Study of Atherosclerosis individual response to vitamin D trial: Building a randomized clinical trial into an observational cohort study.</pubmed_title><pmcid>PMC8089051</pmcid><funding_grant_id>UL1 TR001420</funding_grant_id><funding_grant_id>UL1 TR001881</funding_grant_id><funding_grant_id>R01 HL071205</funding_grant_id><funding_grant_id>UL1 RR033176</funding_grant_id><funding_grant_id>N01HC95159</funding_grant_id><funding_grant_id>75N92020D00007</funding_grant_id><funding_grant_id>UL1 RR025005</funding_grant_id><funding_grant_id>75N92020D00001</funding_grant_id><funding_grant_id>75N92020D00002</funding_grant_id><funding_grant_id>T32 DK007467</funding_grant_id><funding_grant_id>P30 DK035816</funding_grant_id><funding_grant_id>75N92020D00005</funding_grant_id><funding_grant_id>75N92020D00006</funding_grant_id><funding_grant_id>75N92020D00003</funding_grant_id><funding_grant_id>75N92020D00004</funding_grant_id><funding_grant_id>UL1 TR000040</funding_grant_id><funding_grant_id>R01 HL096875</funding_grant_id><funding_grant_id>HHSN268201500003C</funding_grant_id><funding_grant_id>R01 HL071259</funding_grant_id><funding_grant_id>N01HC95160</funding_grant_id><funding_grant_id>R01 HL071258</funding_grant_id><funding_grant_id>UL1 TR001079</funding_grant_id><funding_grant_id>N01HC95161</funding_grant_id><funding_grant_id>N01HC95162</funding_grant_id><funding_grant_id>N01HC95163</funding_grant_id><funding_grant_id>P30 DK017047</funding_grant_id><funding_grant_id>N01HC95164</funding_grant_id><funding_grant_id>N01HC95165</funding_grant_id><funding_grant_id>R01 HL071051</funding_grant_id><funding_grant_id>N01HC95166</funding_grant_id><funding_grant_id>R01 HL071251</funding_grant_id><funding_grant_id>N01HC95167</funding_grant_id><funding_grant_id>N01HC95168</funding_grant_id><funding_grant_id>R01 HL071250</funding_grant_id><funding_grant_id>N01HC95169</funding_grant_id><funding_grant_id>R01 HL071252</funding_grant_id><funding_grant_id>R01 DK088762</funding_grant_id><funding_grant_id>R01 DK099199</funding_grant_id><funding_grant_id>HHSN268201500003I</funding_grant_id><pubmed_authors>Watson KE</pubmed_authors><pubmed_authors>Psaty BM</pubmed_authors><pubmed_authors>Hoofnagle AN</pubmed_authors><pubmed_authors>Rotter JI</pubmed_authors><pubmed_authors>Rice KM</pubmed_authors><pubmed_authors>Williams K</pubmed_authors><pubmed_authors>Siscovick DS</pubmed_authors><pubmed_authors>Liu KJ</pubmed_authors><pubmed_authors>Burke GL</pubmed_authors><pubmed_authors>Allen NB</pubmed_authors><pubmed_authors>Hsu S</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Prince DK</pubmed_authors><pubmed_authors>de Boer IH</pubmed_authors><pubmed_authors>Michos ED</pubmed_authors><pubmed_authors>Tracy RP</pubmed_authors><pubmed_authors>Kestenbaum BR</pubmed_authors><pubmed_authors>McClelland RL</pubmed_authors><pubmed_authors>Shea SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Multi-Ethnic Study of Atherosclerosis individual response to vitamin D trial: Building a randomized clinical trial into an observational cohort study.</name><description>The INdividual response to VITamin D (INVITe) trial was a randomized, placebo-controlled, parallel group trial of vitamin D&lt;sub>3&lt;/sub> supplementation (2000 IU daily) designed to determine clinical and genetic characteristics that modify the response to vitamin D supplementation. To enhance internal and external validity and reduce cost, the INVITe trial was nested within the Multi-Ethnic Study of Atherosclerosis (MESA), an ongoing prospective observational cohort study. The INVITe trial enrolled a community-based population of 666 racially and ethnically diverse participants from January 2017 to April 2019. This represents 30% of 2210 MESA participants approached for screening, and 96% of those found to be eligible. Barriers to enrollment included delayed initiation of the trial relative</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-04T23:02:24.135Z</modification><creation>2025-04-04T23:02:24.135Z</creation></dates><accession>S-EPMC8089051</accession><cross_references><pubmed>33588078</pubmed><doi>10.1016/j.cct.2021.106318</doi></cross_references></HashMap>