How well do participants think their rights are protected
Problem
1. What are potential triggers for human research participants? How can those triggers be addressed?
2. How well do participants think their rights are protected?
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What criteria did the authors set as the clinical definition of a case? What characteristic of the social network is thought to account for this pattern?
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What are potential triggers for human research participants? How can those triggers be addressed? How well do participants think their rights are protected?
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