Patient and Proxy Recall After Providing Written or Oral Informed Consent to Participate in an Interventional Trial.
rct · Level II
Where this comes from
- Record sourced from PubMed, PMID 35560052.
- Also identified by DOI 10.1001/jamanetworkopen.2022.14052 and PMC identifier 9107023.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
This cohort study assesses recall rates among patients and their proxies who consented to participate in a randomized clinical trial.
Medical subject headings
- Informed Consent
- Proxy