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  1. The myth of informed consent: in daily practice and in clinical trials.W. A. Silverman - 1989 - Journal of Medical Ethics 15 (1):6-11.
    Until about thirty years ago, the extent of disclosure about and consent-seeking for medical interventions was influenced by a beneficence model of professional behaviour. Informed consent shifted attention to a duty to respect the autonomy of patients. The new requirement arrived on the American scene in two separate contexts: for daily practice in 1957, and for clinical study in 1966. A confusing double standard has been established. 'Daily consent' is reviewed, if at all, only in retrospect. Doctors are merely exhorted (...)
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  • (1 other version)The psychological profile of parents who volunteer their children for clinical research: a controlled study.Y. H. Thong S. C. Harth, R. R. Johnstone - 1992 - Journal of Medical Ethics 18 (2):86.
    Three standard psychometric tests were administered to parents who volunteered their children for a randomised, double-blind placebo-controlled trial of a new asthma drug and to a control group of parents whose children were eligible for the trial but had declined the invitation. The trial took place at a children's hospital in Australia. The subjects comprised 68 parents who had volunteered their children and 42 who had not, a participation rate of 94 per cent and 70 per cent, respectively. The responses (...)
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  • Women and health research: ethical and legal issues of including women in clinical studies.Anna C. Mastroianni, Ruth R. Faden & Daniel D. Federman (eds.) - 1994 - Washington, D.C.: National Academy Press.
    Executive Summary There is a general perception that biomedical research has not given the same attention to the health problems of women that it has given ...
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  • (1 other version)The psychological profile of parents who volunteer their children for clinical research: a controlled study.S. C. Harth, R. R. Johnstone & Y. H. Thong - 1992 - Journal of Medical Ethics 18 (2):86-93.
    Three standard psychometric tests were administered to parents who volunteered their children for a randomised, double-blind placebo-controlled trial of a new asthma drug and to a control group of parents whose children were eligible for the trial but had declined the invitation. The trial took place at a children's hospital in Australia. The subjects comprised 68 parents who had volunteered their children and 42 who had not, a participation rate of 94 per cent and 70 per cent, respectively. The responses (...)
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