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Implementing a New Common Rule Requirement for Informed Consent: A Randomized Trial on Adult Asthma Patients
Objectives. To determine how the format of a clinical trial informed consent document can affect participants’ retention of enrollment-relevant information. Background. Recent changes to the US Federal Common Rule require informed consent documents for clinical trials to be concise and start with th...
Guardat en:
| Publicat a: | MDM Policy Pract |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6440037/ https://ncbi.nlm.nih.gov/pubmed/30944885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2381468319839315 |
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