Informed consent to biomedical research in Veterans Administration Hospitals

JAMA. 1982 Jul 16;248(3):344-8.

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.

KIE: Patients and physicians involved in research projects in four Veterans Administration hospitals were interviewed about their experiences with informed consent. Results showed that most patients knew that they were research subjects, had voluntarily consented, and knew details of their medical treatment, but few understood the research well. The nature of the consent forms, the person explaining the research and the manner of explanation, and, in some cases, the degree of illness were factors affecting subjects' awareness.

Publication types

  • Clinical Trial

MeSH terms

  • Awareness
  • Clinical Trials as Topic
  • Comprehension*
  • Consent Forms
  • Consumer Behavior
  • Hospitals, Veterans*
  • Humans
  • Informed Consent*
  • Male
  • Motivation
  • Research Subjects
  • Research*
  • United States