The US Department of Health and Human Services addresses clear communication in the informed consent process as part of the Notice of Proposed Rulemaking for revisions to the Common Rule. However, prior research has shown that participants may not fully comprehend research studies despite completion of an informed consent process. Our main goal was to provide plain language information about donation processes to a cancer biobank to supplement an informed consent form. We developed and conducted cognitive testing with supplemental brochures that clearly communicated information about three different models for consent (notice, broad and study-specific) to future use of biospecimens. During the brochure development process, we conducted qual...
Aims: The purpose of this study was to analyze the content of informed consent forms for clinical tr...
The problem: We are investigating if biological material with human DNA sequence data is being colle...
Researchers and policymakers do not agree about the most appropriate way to get consent for the use ...
The US Department of Health and Human Services addresses clear communication in the informed consent...
Consent forms have lengthened over time and become harder for participants to understand. We sought ...
Biobanks are essential resources, and participation by individuals from diverse groups is needed. Va...
BackgroundClinical genomic implementation studies pose challenges for informed consent. Consent form...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Purpose: Studies have documented that the majority of consent documents for medical diagnosis and tr...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
The signed informed consent form provides documentary evidence that the patient has given informed c...
Informed consent models designed to appropriately regulate biobank-based research are characterized ...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Aims: The purpose of this study was to analyze the content of informed consent forms for clinical tr...
The problem: We are investigating if biological material with human DNA sequence data is being colle...
Researchers and policymakers do not agree about the most appropriate way to get consent for the use ...
The US Department of Health and Human Services addresses clear communication in the informed consent...
Consent forms have lengthened over time and become harder for participants to understand. We sought ...
Biobanks are essential resources, and participation by individuals from diverse groups is needed. Va...
BackgroundClinical genomic implementation studies pose challenges for informed consent. Consent form...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Purpose: Studies have documented that the majority of consent documents for medical diagnosis and tr...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
The signed informed consent form provides documentary evidence that the patient has given informed c...
Informed consent models designed to appropriately regulate biobank-based research are characterized ...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Aims: The purpose of this study was to analyze the content of informed consent forms for clinical tr...
The problem: We are investigating if biological material with human DNA sequence data is being colle...
Researchers and policymakers do not agree about the most appropriate way to get consent for the use ...