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• W1965023384 abstract "Stineman MG, Musick DW. Protection of human subjects with disability: guidelines for research. Arch Phys Med Rehabil 2001;82 Suppl 2:S9-14. Typically, protection of human subjects is a shared responsibility involving the local institutional review board (IRB) and the clinical investigator, guided by federal and state law as well as local organizational policy. The IRB screens protocols to ensure subjects' safety by making sure that risks are acceptable and do not outweigh benefits. However, the recruitment of subjects, as well as obtaining consent, is the principal investigator's responsibility. Through the process of informed consent, the clinical investigator is obliged to ensure that each subject understands all treatments proposed and their potential benefits and risks. Achieving truly informed consent from people with major developmental, physical, sensory, communicative, or cognitive disabilities may be particularly difficult. Spurred on by increasing research of relevance to rehabilitation medicine and the patients served, we review legal, ethical, and moral issues surrounding the processes of obtaining informed consent and offer specific recommendations for protecting people with disabilities. © 2001 by the American Congress of Rehabilitation Medicine" @default.
• W1965023384 created "2016-06-24" @default.
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• W1965023384 date "2001-12-01" @default.
• W1965023384 modified "2023-09-26" @default.
• W1965023384 title "Protection of human subjects with disability: Guidelines for research" @default.
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• W1965023384 doi "https://doi.org/10.1053/apmr.2001.31002" @default.
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