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  1. Improving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process.P. Allmark - 2006 - Journal of Medical Ethics 32 (8):439-443.
    Objective: To assess whether continuous consent, a process in which information is given to research participants at different stages in a trial, and clinician training in that process were effective when used by clinicians while gaining consent to the Total Body Hypothermia (TOBY) trial. The TOBY trial is a randomised controlled trial (RCT) investigating the use of whole-body cooling for neonates with evidence of perinatal asphyxia. Obtaining valid informed consent for the TOBY trial is difficult, but is a good test (...)
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  • Depression and competence to refuse psychiatric treatment.A. Rudnick - 2002 - Journal of Medical Ethics 28 (3):151-155.
    Individuals with major depression may benefit from psychiatric treatment, yet they may refuse such treatment, sometimes because of their depression. Hence the question is raised whether such individuals are competent to refuse psychiatric treatment. The standard notion of competence to consent to treatment, which refers to expression of choice, understanding of medical information, appreciation of the personal relevance of this information, and logical reasoning, may be insufficient to address this question. This is so because major depression may not impair these (...)
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