Physicians' Understanding of Consent Requirements for Phase I Clinical Trials in Cognitively Impaired or Highly Vulnerable Patients
Farber, Neil J.
Aboff, Brian M.
DeJoseph, Maria R.
Boyer, E. Gil
Accountability in Research 2004 January-March; 11(1): 63-78
We investigated physicians' attitudes about entering patients who cannot give informed consent or who are of a vulnerable population into clinical trials. A survey instrument asked a nationwide sample of practicing physicians about whether ten hypothetical patients could be enrolled in a phase I clinical trials. The impact of demographic variables on the number of scenarios viewed as completely or somewhat acceptable was analyzed via student's T tests or analysis of variance (ANOVA) as applicable. All significant (p
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Farber, Neil J.; Gilibert, Stephanie G.; Aboff, Brian M.; Collier, Virginia U.; Weiner, Joan; Boyer, E. Gil (2005-10)
Farber, Neil J.; Aboff, Brian M.; Weiner, Joan; Davis, Elizabeth B.; Boyer, E. Gil; Ubel, Peter A. (2001-11-20)
Farber, Neil J; Roche, Charles V 3rd.; Aboff, Brian M; Collier, Virginia U; Weiner, Joan (2010-06)OBJECTIVE: Despite ethical implications, there are anecdotal reports of health practitioners withholding services from patients who do not pay their bills. We surveyed physicians about their attitudes and experiences ...