Long term clinical trials: how much information do participants retain from the informed consent process?

Griffin, Joan M; Struve, James K; Collins, Dorothea; Liu, An; Nelson, David B; Bloomfield, Hanna E

Griffin, Joan M; Struve, James K; Collins, Dorothea; Liu, An; Nelson, David B; Bloomfield, Hanna E.

Affiliation

Griffin JM; Center for Chronic Disease Outcomes Research, Minneapolis VA Medical Center, MN, USA. Joan.griffin2@med.va.gov

Contemp Clin Trials ; 27(5): 441-8, 2006 Oct.

Article in En | MEDLINE | ID: mdl-16798101

Subject(s)

Clinical Trials as Topic; Informed Consent; Memory; Age Factors; Aged; Cholesterol, HDL; Educational Status; Gemfibrozil/therapeutic use; Humans; Hypolipidemic Agents/therapeutic use; Logistic Models; Male; Marital Status; Racial Groups; Randomized Controlled Trials as Topic

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Collection: 01-internacional Database: MEDLINE Main subject: Clinical Trials as Topic / Informed Consent / Memory Type of study: Clinical_trials / Prognostic_studies Aspects: Equity_inequality / Ethics Limits: Aged / Humans / Male Language: En Journal: Contemp Clin Trials Journal subject: MEDICINA / TERAPEUTICA Year: 2006 Document type: Article Affiliation country: United States Country of publication: United States

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