Literature DB >> 7045434

Informed consent to biomedical research in Veterans Administration Hospitals.

H W Riecken, R Ravich.   

Abstract

To illuminate the process of obtaining informed consent to research in a medically dependent population, we interviewed 156 patients and 37 physicians involved in research projects at four Veterans Administration hospitals. Most patients knew they were research subjects, had voluntarily consented, and knew the details of their medical treatment, but few understood the research well. Readability analysis indicated that consent forms required college-level education. Twenty-eight percent of patients were not aware of their participation in research although they had signed consent forms. No single act, omission, or personal attribute completely explains this unawareness, but it is associated with incomplete consent forms, the identity of the person explaining the research, the manner of the explanation, and, in some cases, grave illness.

Entities:  

Keywords:  Biomedical and Behavioral Research

Mesh:

Year:  1982        PMID: 7045434

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  24 in total

Review 1.  Improving the informed consent process for research subjects with low literacy: a systematic review.

Authors:  Leonardo Tamariz; Ana Palacio; Mauricio Robert; Erin N Marcus
Journal:  J Gen Intern Med       Date:  2012-07-11       Impact factor: 5.128

2.  Satisfying patients' rights in Iran: Providing effective strategies.

Authors:  Zohreh Anbari; Mehri Mohammadi; Magid Taheri
Journal:  Iran J Nurs Midwifery Res       Date:  2015 Mar-Apr

3.  Motivations, understanding, and voluntariness in international randomized trials.

Authors:  Nancy E Kass; Suzanne Maman; Joan Atkinson
Journal:  IRB       Date:  2005 Nov-Dec

Review 4.  The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countries.

Authors:  Amulya Mandava; Christine Pace; Benjamin Campbell; Ezekiel Emanuel; Christine Grady
Journal:  J Med Ethics       Date:  2012-02-07       Impact factor: 2.903

5.  Using formative research to develop a context-specific approach to informed consent for clinical trials.

Authors:  Amy L Corneli; Margaret E Bentley; James R Sorenson; Gail E Henderson; Charles van der Horst; Agnes Moses; Jacqueline Nkhoma; Lyson Tenthani; Yusuf Ahmed; Charles M Heilig; Denise J Jamieson
Journal:  J Empir Res Hum Res Ethics       Date:  2006-12       Impact factor: 1.742

6.  The use of multimedia in the informed consent process.

Authors:  H B Jimison; P P Sher; R Appleyard; Y LeVernois
Journal:  J Am Med Inform Assoc       Date:  1998 May-Jun       Impact factor: 4.497

Review 7.  The doctor's duty to the elderly patient in clinical trials.

Authors:  Antony Bayer; Mark Fish
Journal:  Drugs Aging       Date:  2003       Impact factor: 3.923

8.  Informed consent in clinical research with drugs in Spain: perspective of clinical trials committee members.

Authors:  R Dal-Ré
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

9.  Do psychiatric patients need greater protection than medical patients when they consent to treatment?

Authors:  F Cournos
Journal:  Psychiatr Q       Date:  1993

10.  Purpose and benefits of early phase cancer trials: what do oncologists say? What do patients hear?

Authors:  Nancy Kass; Holly Taylor; Linda Fogarty; Jeremy Sugarman; Steven N Goodman; Annallys Goodwin-Landher; Michael Carducci; Herbert Hurwitz
Journal:  J Empir Res Hum Res Ethics       Date:  2008-09       Impact factor: 1.742

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