Translations of informed consent documents for clinical trials in South Africa: are they readable?
1. Introduction: Obtaining Informed consent is an ethical prerequisite for enrollment in clinical research. There is a perception that Informed consent documents used in biomedical research are lengthy, overly complex and above the reading capability of typical research participants. In South Africa...
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| Format: | Dissertation |
| Language: | English |
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Faculty of Health Sciences
2020
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| Online Access: | http://hdl.handle.net/11427/31021 |