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Patient and Proxy Recall After Providing Written or Oral Informed Consent to Participate in an Interventional Trial
This cohort study assesses recall rates among patients and their proxies who consented to participate in a randomized clinical trial.
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
American Medical Association
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107023/ https://www.ncbi.nlm.nih.gov/pubmed/35560052 http://dx.doi.org/10.1001/jamanetworkopen.2022.14052 |