Search Results - "Brelsford, Kathleen"
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Direct-to-consumer genetic testing: Prospective users' attitudes toward information about ancestry and biological relationships
Published in PloS one (29-11-2021)“…Direct-to-consumer genetic testing is marketed as a tool to uncover ancestry and kin. Recent studies of actual and potential users have demonstrated that…”
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Thought leader perspectives on benefits and harms in precision medicine research
Published in PloS one (26-11-2018)“…Precision medicine research is underway to identify targeted approaches to improving health and preventing disease. However, such endeavors raise significant…”
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Surgeon Perspectives on Benefits and Downsides of Overlapping Surgery: In-depth, Qualitative Interviews
Published in Annals of surgery (01-11-2021)“…OBJECTIVE:The aim of the study was to characterize surgeon perspectives regarding the benefits and downsides of conducting overlapping surgery…”
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Patient perspectives on use of electronic health records for research recruitment
Published in BMC medical research methodology (26-02-2019)“…EHR phenotyping offers the ability to rapidly assemble a precisely defined cohort of patients prescreened for eligibility to participate in health-related…”
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Patient values regarding overlapping surgery: Identification of distinct patient subgroups
Published in The Laryngoscope (01-12-2020)“…Objectives/Hypothesis To explore patient values associated with their comfort level with surgical trainees and attending surgeon absence from the operating…”
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Research use of electronic health records: patients' perspectives on contact by researchers
Published in Journal of the American Medical Informatics Association : JAMIA (01-09-2018)“…The use of electronic health records (EHRs) for research has the potential to improve the diagnosis and treatment of disease, yet contact with patients based…”
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Trust as a Predictor of Patient Perceptions Regarding Overlapping Surgery and Trainee Independence
Published in The Laryngoscope (01-11-2020)“…Objectives To examine opinions on trainee independence and attending presence among a cross‐section of the general population and explore how perceptions of…”
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Developing model biobanking consent language: what matters to prospective participants?
Published in BMC medical research methodology (15-05-2020)“…Efforts to improve informed consent have led to calls for providing information a reasonable person would want to have, in a way that facilitates understanding…”
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Mapping parents' journey following prenatal diagnosis of CHD: a qualitative study
Published in Cardiology in the young (01-08-2023)“…To better understand parents' accounts of their prenatal and postnatal experience after prenatal diagnosis of CHD - particularly emotional processing and…”
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Uncertainty of Prenatally Diagnosed Congenital Heart Disease: A Qualitative Study
Published in JAMA network open (01-05-2020)“…Parents who receive a prenatal diagnosis of congenital heart disease may experience more short- and long-term stress than those who receive a postnatal…”
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Patient Perceptions of Resident Involvement in Surgery: A Qualitative Study Using Surgical Video
Published in Journal of surgical education (01-07-2022)“…To improve patient-centered perioperative informed consent, this study used real surgical footage to identify key topics which might be discussed with patients…”
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Thought Leader Perspectives on Participant Protections in Precision Medicine Research
Published in The Journal of law, medicine & ethics (01-03-2019)“…Precision medicine research is rapidly taking a lead role in the pursuit of new ways to improve health and prevent disease, but also presents new challenges…”
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Ethical Considerations in the Conduct of Unregulated mHealth Research: Expert Perspectives
Published in The Journal of law, medicine & ethics (01-03-2020)“…To assist in resolving ethical questions surrounding unregulated mHealth research, we conducted in-depth qualitative interviews with experts from four key…”
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Mapping Parents’ Journey Following Prenatal Diagnosis of Congenital Heart Disease (T315C)
Published in Journal of pain and symptom management (01-03-2021)“…Objectives 1. Describe Results from this analysis on how parents process and cope after receiving a prenatal diagnosis of congenital heart disease. 2…”
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Protecting Participants in Genomic Research: Understanding the “Web of Protections” Afforded by Federal and State Law
Published in The Journal of law, medicine & ethics (01-03-2020)“…Researchers now commonly collect biospecimens for genomic analysis together with information from mobile devices and electronic health records. This rich…”
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Comparison of Approaches for Notification and Authorization in Pragmatic Clinical Research Evaluating Commonly Used Medical Practices
Published in Medical care (01-11-2017)“…For pragmatic clinical research comparing commonly used treatments, questions exist about if and how to notify participants about it and secure their…”
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Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations
Published in The Journal of law, medicine & ethics (01-03-2020)“…Mobile devices with health apps, direct-to-consumer genetic testing, crowd-sourced information, and other data sources have enabled research by new classes of…”
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Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance
Published in The Journal of law, medicine & ethics (01-03-2018)“…Neither the range of potential results from genomic research that might be returned to participants nor future uses of stored data and biospecimens can be…”
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Culture and Context: Buffering the Relationship Between Stressful Life Events and Risky Behaviors in American Indian Youth
Published in Substance use & misuse (29-07-2011)“…The Sacred Mountain Youth Project was conducted to investigate risk and protective factors related to alcohol and drug use among American Indian youth…”
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Expert Perspectives on Oversight for Unregulated mHealth Research: Empirical Data and Commentary
Published in The Journal of law, medicine & ethics (01-03-2020)“…In qualitative interviews with a diverse group of experts, the vast majority believed unregulated researchers should seek out independent oversight. Reasons…”
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