Statements in which the resource exists.
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pubmed-article:1941028pubmed:abstractTextInformed consent has been indirectly studied only in settings that do not replicate the actual consent process. We designed a sham study and randomly allocated adult ambulatory patients to receive one of two consent forms: Consent A (n = 52) described a randomized trial of usual treatment vs a new medication that "may work twice as fast as the usual treatment"; or Consent B (n = 48) that described a randomized trial of a new medication that "may work half as fast as the usual treatment". Patients randomized to Consent A were more likely to consent than those randomized to Consent B (consent rate A = 67%, consent rate B = 42%, p less than 0.01). Among patients who cited quantitative information, the difference in consent rate was even more marked (95% vs 36%, p less than 0.001); patients who did not cite quantitative information had equivalent consent rates. Patients who perceived minimal or severe symptoms had lower consent rates than those with mid-range symptom scores (chi 2(2) = 8.35, p = 0.015). Patients who recognize quantitative information will use it to make informed consent decisions.lld:pubmed
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pubmed-article:1941028pubmed:authorpubmed-author:FeussnerJ RJRlld:pubmed
pubmed-article:1941028pubmed:authorpubmed-author:SimelD LDLlld:pubmed
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pubmed-article:1941028pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1941028pubmed:year1991lld:pubmed
pubmed-article:1941028pubmed:articleTitleA randomized controlled trial comparing quantitative informed consent formats.lld:pubmed
pubmed-article:1941028pubmed:affiliationAmbulatory Care Service, Durham Veterans Administration Medical Center, North Carolina 27705.lld:pubmed
pubmed-article:1941028pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1941028pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:1941028pubmed:publicationTypeRandomized Controlled Triallld:pubmed
pubmed-article:1941028pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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