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期刊名:Ethics & human research

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ISSN:2578-2363

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共收录本刊相关文章索引212
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Carmel Shachar,Sara Gerke,Walker Morrell et al. Carmel Shachar et al.
Digital applications (apps) are commonly used across the research ecosystem. While apps are frequently updated in the course of clinical and behavioral research, there is limited guidance as to when an app update should trigger action relat...
Jane Paik Kim,Sangeeta Mondal,Tenzin Tsungmey et al. Jane Paik Kim et al.
Research participants should be drawn as fairly as possible from the potential volunteer population. Underlying personality traits are underexplored as factors influencing research decision-making. Dispositional optimism, known to affect co...
Ian Tully Ian Tully
Research on mental health and illness presents a variety of unique ethical challenges. This article argues that institutional review boards (IRBs) can improve their reviews of such research by including the perspectives of individuals with ...
Kemesha Gabbidon,Tiffany Chenneville,Wendy Rote Kemesha Gabbidon
Over the last few years, the use of dyadic research methods has expanded considerably. One area that has benefited from this type of research is the study of the family unit, particularly parent-adolescent dyads. Dyadic research allows inve...
Mikaela Matera-Vatnick,Katherine W Todman,Paul G Wakim et al. Mikaela Matera-Vatnick et al.
Occasionally, the ability of prospective research participants to consent may be uncertain. Yet standardized capacity-assessment tools may not suffice to determine the ability to consent to a particular research protocol. This study consist...
Neal W Dickert,Kathleen Metz,S Iris Deeds et al. Neal W Dickert et al.
Informed consent for clinical trials in acute stroke is characterized by challenges related to urgency, cognitive impairment, and geographical separation. Context-appropriate approaches are needed for this setting. We conducted a mixed-meth...
Kimberley Serpico,Vasiliki Rahimzadeh,Emily E Anderson et al. Kimberley Serpico et al.
Institutional review boards (IRBs) are permitted by regulation to seek assistance from outside experts when reviewing research applications that are beyond the scope of expertise represented in their membership. There is insufficient unders...
Gavin Campbell,Margie D Dixon,Minisha Lohani et al. Gavin Campbell et al.
In phase I trials, some biospecimens are used both for research and patient care and some for research only. Some research participants have therapeutic misconception, assuming all biospecimens are for patient care. This study's aim was to ...
Sonia Colina,Miriam Rodríguez-Guerra,Nicole Marrone et al. Sonia Colina et al.
To avoid excluding individuals with limited English proficiency from participating in research, the consent form and other documents should be presented to them in their primary language and in a format that is understandable. However, evid...
T J Kasperbauer,Colin Halverson,Abigail Garcia et al. T J Kasperbauer et al.
Biobank participants often do not understand the information they are provided during the informed consent process. Ethicists and other stakeholders have disagreed, however, on the appropriate response to these failures in understanding. Th...