Research Subjects

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  Subject Areas on Research

  • A limited bibliography of the Federal Government-funded human radiation experiments. 
  • A randomized controlled trial comparing quantitative informed consent formats. 
  • Acute effects of trauma-focused research procedures on participant safety and distress. 
  • Are patients with longer emergency department wait times less likely to consent to research? 
  • Are there adverse consequences of quizzing during informed consent for HIV research? 
  • Assessment of the Perceived Acceptability of an Early Enrollment Strategy Using Advance Consent in Health Care-Associated Pneumonia. 
  • Attitudes toward clinical trials among patients with sickle cell disease. 
  • Attitudes, knowledge, and risk perceptions of women with breast and/or ovarian cancer considering testing for BRCA1 and BRCA2. 
  • Biodefence and the production of knowledge: rethinking the problem. 
  • Can research participants comment authoritatively on the validity of their self-reports of mind wandering and task engagement? 
  • Can underpowered clinical trials be justified? 
  • Certificates of confidentiality and informed consent: perspectives of IRB chairs and institutional legal counsel. 
  • Characteristics of REPRIEVE Trial Participants Identifying Across the Transgender Spectrum. 
  • Common Data Elements for Subarachnoid Hemorrhage and Unruptured Intracranial Aneurysms: Recommendations from the Working Group on Subject Characteristics. 
  • Comparison of Approaches for Notification and Authorization in Pragmatic Clinical Research Evaluating Commonly Used Medical Practices. 
  • Conducting empirical research on informed consent: challenges and questions 
  • Confidentiality: more than a linkage file and a locked drawer. 
  • Consent (assent) for research with pediatric patients 
  • Consent forms and the therapeutic misconception: the example of gene transfer research. 
  • Considering the Benefits and Risks of Research Participants' Access to Sequence Data. 
  • Data monitoring and interim analyses in the pharmaceutical industry: ethical and logistical considerations. 
  • Determinants of a subject's decision to participate in clinical anesthesia research. 
  • Developing model language for disclosing financial interests to potential clinical research participants. 
  • Disclosing conflicts of interest in clinical research: views of institutional review boards, conflict of interest committees, and investigators. 
  • Disclosure of financial relationships to participants in clinical research. 
  • Effects of disclosing financial interests on attitudes toward clinical research. 
  • Empirical research on informed consent. An annotated bibliography. 
  • Ethical considerations for involving Latina adolescents in mental health research. 
  • Ethical dilemma in continuing a zidovudine-placebo trial in symptomatic human immunodeficiency virus infection. 
  • Exploring the "legacy" of the Tuskegee Syphilis Study: a follow-up study from the Tuskegee Legacy Project. 
  • From trial and error to trial simulation. Part 2: an appraisal of current beliefs in the design and analysis of clinical trials for antidepressant drugs. 
  • Getting meaningful informed consent from older adults: a structured literature review of empirical research. 
  • How can we draw the line between clinical care and medical research. 
  • I'll be a monkey's uncle: a moral challenge to human genetic enhancement research. 
  • Immunization and the American way: 4 childhood vaccines. 
  • Impact of Cognitive Impairment Across Specialties: Summary of a Report From the U13 Conference Series. 
  • Impact of pediatric exclusivity on drug labeling and demonstrations of efficacy. 
  • Influence of clinical trial participation on subsequent antithrombin use. 
  • Informed consent for research in Borderline Personality Disorder. 
  • Innovation in Clinical Research Regulation. 
  • Issues affecting minority participation in research studies of Alzheimer disease. 
  • Knowledge Gaps in Cardiovascular Care of the Older Adult Population: A Scientific Statement From the American Heart Association, American College of Cardiology, and American Geriatrics Society. 
  • Let the punishment fit the crime: sensible consent in the management of human subjects research and standard-of-care interventions. 
  • Leveraging a Landmark Trial of Primary Cardiovascular Disease Prevention in Human Immunodeficiency Virus: Introduction From the REPRIEVE Coprincipal Investigators. 
  • Mechanisms to provide safe and effective drugs for children. 
  • Medical, ethical and legal issues regarding thrombolytic therapy in the Jehovah's Witness. 
  • Older Adults in Clinical Research and Drug Development: Closing the Geriatric Gap. 
  • Oversight mechanisms for clinical research. 
  • Participants' perspectives on safety monitoring in clinical trials. 
  • Partnering with engaged patients accelerates research. 
  • Patient reactions to confidentiality, liability, and financial aspects of informed consent in cardiology research. 
  • Patients' Views Concerning Research on Medical Practices: Implications for Consent. 
  • Perceptions of African-American culture and implications for clinical trial design. 
  • Perceptions of Equipoise, Risk-Benefit Ratios, and "Otherwise Healthy Volunteers" in the Context of Early-Phase HIV Cure Research in the United States: A Qualitative Inquiry. 
  • Prenatal gene tranfer: scientific, medical, and ethical issues: a report of the Recombinant DNA Advisory Committee. 
  • Promoting the participant-researcher partnership. 
  • Proposal for the American Journal of Transplantation policy for review of ethical standards of clinical research involving live human subjects. 
  • Providing Individual Research Results to Participants-Reply. 
  • Quality improvement and evidence-based practice change projects and the institutional review board: is approval necessary? 
  • Recruiting intergenerational African American males for biomedical research Studies: a major research challenge. 
  • Recruitment and retention: A randomized controlled trial of video-enhanced versus standard consent processes within the E-OPTIMAL study. 
  • Recruitment of rural and cognitively impaired older adults for dental research. 
  • Relationship Between Enrolling Country Income Level and Patient Profile, Protocol Completion, and Trial End Points. 
  • Reporting of Study Participant Demographic Characteristics and Demographic Representation in Premarketing and Postmarketing Studies of Novel Cancer Therapeutics. 
  • Representation of women in randomized clinical trials of cardiovascular disease prevention. 
  • Research ethics. Certificates of confidentiality and compelled disclosure of data. 
  • Return of Research Results to Study Participants: Uncharted and Untested. 
  • Scientific and social issues of human immunodeficiency virus vaccine development. 
  • Sex-Specific Differences in Heart Failure: Pathophysiology, Risk Factors, Management, and Outcomes. 
  • Small Social Incentives Did Not Improve the Survey Response Rate of Patients Who Underwent Orthopaedic Surgery: A Randomized Trial. 
  • Special care unit research: ethical issues. 
  • Start me up: ways to encourage sharing of genomic information with research participants. 
  • Statistical Evaluation of Clinical Trials Under COVID-19 Pandemic. 
  • Suspended judgment. Clinical trials of informed consent. 
  • Systematic review and metasummary of attitudes toward research in emergency medical conditions. 
  • The Controversy Over Retrospective Moral Judgment 
  • The Legal Ethics of Pediatric Research 
  • The Tuskegee Legacy Project: willingness of minorities to participate in biomedical research. 
  • The concept of voluntary consent. 
  • The consent process and children 
  • The ethical challenges of a randomized controlled trial of involuntary outpatient commitment. 
  • The legacy of the Tuskegee Syphilis Study: assessing its impact on willingness to participate in biomedical studies. 
  • The many meanings of care in clinical research. 
  • The potential influence of Internet-based social networking on the conduct of clinical research studies. 
  • Therapeutic misconception in early phase gene transfer trials. 
  • Tolerability of the Oscar 2 ambulatory blood pressure monitor among research participants: a cross-sectional repeated measures study. 
  • Understanding Ethical Issues of Research Participation From the Perspective of Participating Children and Adolescents: A Systematic Review. 
  • Unintended changes in cognition, mood, and behavior arising from cell-based interventions for neurological conditions: ethical challenges. 
  • Urge overkill: protecting deidentified human subjects at what price? 
  • Use of patient-reported outcomes in randomized, double-blind, placebo-controlled clinical trials. 
  • Using Cognitive Interviews to Enhance Measurement in Empirical Bioethics: Developing a Measure of the Preventive Misconception in Biomedical HIV Prevention Trials. 
  • Views of potential research participants on financial conflicts of interest: barriers and opportunities for effective disclosure. 
  • Who should go first in trials with scarce agents? The views of potential participants. 
  • Willingness of Women with Endometriosis Planning to Undergo IVF to Participate in a Randomized Clinical Trial and the Effects of the COVID-19 Pandemic on Potential Participation. 
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  Keywords of People

  • Limkakeng Jr., Alexander Tan, Professor of Emergency Medicine, Emergency Medicine
  • Muhlbaier, Lawrence H., Associate Professor Emeritus of Biostatistics & Bioinformatics, Biostatistics & Bioinformatics
  • Pang, Herbert, Adjunct Assistant Professor in the Department of Biostatistics & Bioinformatics, Biostatistics & Bioinformatics