Making research consent forms informative and understandable: the experience of the Indian Health Service

Camb Q Healthc Ethics. Fall 1994;3(4):510-21. doi: 10.1017/s0963180100005399.
No abstract available

MeSH terms

  • Clinical Trials as Topic / standards
  • Comprehension*
  • Consent Forms*
  • Educational Status
  • Ethics Committees, Research
  • Ethics, Professional
  • Human Rights
  • Humans
  • Indians, North American*
  • Informed Consent*
  • Inuits
  • Personal Autonomy
  • Professional Staff Committees*
  • Researcher-Subject Relations
  • Risk Assessment
  • United States
  • United States Indian Health Service / organization & administration*