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  1. Can the written information to research subjects be improved?--an empirical study.E. Bjorn, P. Rossel & S. Holm - 1999 - Journal of Medical Ethics 25 (3):263-267.
    OBJECTIVES: To study whether linguistic analysis and changes in information leaflets can improve readability and understanding. DESIGN: Randomised, controlled study. Two information leaflets concerned with trials of drugs for conditions/diseases which are commonly known were modified, and the original was tested against the revised version. SETTING: Denmark. PARTICIPANTS: 235 persons in the relevant age groups. MAIN MEASURES: Readability and understanding of contents. RESULTS: Both readability and understanding of contents was improved: readability with regard to both information leaflets and understanding with (...)
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  • False Hopes and Best Data: Consent to Research and the Therapeutic Misconception.Paul S. Appelbaum, Loren H. Roth, Charles W. Lidz, Paul Benson & William Winslade - 1987 - Hastings Center Report 17 (2):20-24.
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  • Experienced consent in geriatrics research: a new method to optimize the capacity to consent in frail elderly subjects.M. G. Rikkert, J. H. van den Bercken, H. A. ten Have & W. H. Hoefnagels - 1997 - Journal of Medical Ethics 23 (5):271-276.
    OBJECTIVES: Cognitive and sensory difficulties frequently jeopardize informed consent of frail elderly patients This study is the first to test whether preliminary research experience could enhance geriatric patients' capacity to consent. DESIGN/SETTING: A step-wise consent procedure was introduced in a study on fluid balance in geriatric patients. Eligible patients providing verbal consent participated in a try-out of a week, during which bioelectrical impedance and weight measurements were performed daily. Afterwards, written informed consent was requested. Comprehension, risk and inconvenience scores (ranges: (...)
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  • Ethical Aspect of Research Involving Elderly Subjects.John C. Fletcher - 1990 - Journal of Clinical Ethics 1 (4):285-286.
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