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The purpose of this study is to determine the effectiveness of needlestick injury prevention module
Full description
After being informed about the study and the potential risk, participants were given written informed consent to be filled out and signed. Agreed participants will receive a 1-week duration of educational intervention. The intervention only involved education and was less likely to cause injury or damage to the body.
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Interventional model
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90 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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