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266 results on '"Research Personnel"'

1. Informed consent for Alzheimer's disease clinical trials: a survey of clinical investigators.

Author

Karlawish, Jason HT, Knopman, David, Clark, Christopher M, Morris, John C, Marson, Daniel, Whitehouse, Peter J, and Kawas, Claudia H

Subjects
Humans, Alzheimer Disease, Data Collection, Health Knowledge, Attitudes, Practice, Mental Competency, Patient Selection, State Government, Government Regulation, Informed Consent, Consent Forms, Third-Party Consent, Ethics Committees, Research, Proxy, Research Personnel, Research Subjects, United States, Clinical Trials as Topic, Biomedical and Behavioral Research, Empirical Approach, Applied Ethics
Published
2002

2. Parent and Child Perceptions of the Benefits of Research Participation

Author

Victoria A, Miller and Chris, Feudtner

Subjects
Parents, Biomedical Research, Informed Consent, Adolescent, Humans, Perception, Patient Participation, Child, Research Personnel
Abstract

The primary objective of this study was to describe parents' and children's perceptions of the health benefits of research participation. We assessed 180 children ages 8 to 17 years who recently enrolled in medical research and their parents. Of the 136 parents with children on observational protocols, 41% indicated that there would be a health benefit to the child. Their descriptions of benefits revealed that many envisioned a future health benefit to the child arising from improvements in treatment due to the research. There was no difference in ratings of likelihood or importance of benefit between parents of children enrolled in observational protocols versus interventional protocols. Children enrolled in observational protocols were more likely to respond "don't know" to the question about potential health benefit compared to children on interventional protocols. For both observational and interventional protocols, the informed consent process may be enhanced when research personnel explicitly differentiate between different types of potential benefits, including heretofore-unrecognized future direct health benefits.

Published
2018

7. Research biopsies in phase I studies: views and perspectives of participants and investigators

Author

Rebecca D, Pentz, R Donald, Harvey, Margaret, White, Zachary Luke, Farmer, Olga, Dashevskaya, Zhengjia, Chen, Colleen, Lewis, Taofeek K, Owonikoko, and Fadlo R, Khuri

Subjects
Adult, Aged, 80 and over, Male, Informed Consent, Clinical Trials, Phase I as Topic, Research Subjects, Biopsy, Beneficence, Middle Aged, Risk Assessment, Research Personnel, Article, Ethics, Research, Attitude, Humans, Female, Comprehension, Aged
Published
2012

13. Protecting third parties in human subjects research

Author

David B, Resnik and Richard R, Sharp

Subjects
Safety Management, Research Subjects, Federal Government, Disclosure, Risk Assessment, Hazardous Substances, Article, Researcher-Subject Relations, Pregnancy, Humans, Family, Pesticides, Third-Party Consent, Social Responsibility, Data Collection, Beneficence, Liability, Legal, Health Surveys, Research Personnel, United States, Pedigree, Human Experimentation, Privacy, Government Regulation, Female, Pregnant Women, Ethics Committees, Research
Published
2006

14. Part I: what is the requirement for data sharing?

Author

Virginia A, de Wolf, Joan E, Sieber, Philip M, Steel, and Alvan O, Zarate

Subjects
Access to Information, Biomedical Research, Human Experimentation, Informed Consent, Information Dissemination, Research Subjects, Interprofessional Relations, Humans, Confidentiality, Research Personnel, United States, Behavioral Research, Ethics Committees, Research
Published
2006

15. Informed consent: practices and views of investigators in a multinational clinical trial

Author

Lindsay, Sabik, Christine A, Pace, Heidi P, Forster-Gertner, David, Wendler, Judith D, Bebchuk, Jorge A, Tavel, Laura A, McNay, Jack, Killen, Ezekiel J, Emanuel, and Christine, Grady

Subjects
Risk, Health Knowledge, Attitudes, Practice, Informed Consent, Internationality, Research Subjects, Data Collection, HIV Infections, Disclosure, Research Personnel, United States, Consent Forms, Researcher-Subject Relations, Human Experimentation, Clinical Trials, Phase III as Topic, Humans, Multicenter Studies as Topic, Comprehension, Randomized Controlled Trials as Topic
Published
2006

16. Bounty-hunting and finder's fees

Author

James A, Christensen and James P, Orlowski

Subjects
Clinical Trials as Topic, Motivation, Physician-Patient Relations, Biomedical Research, Informed Consent, Conflict of Interest, Research Subjects, Health Personnel, Patient Selection, Disclosure, Research Personnel, Researcher-Subject Relations, Fees and Charges, Research Support as Topic, Humans, Industry, Referral and Consultation
Published
2005

18. The certificate of confidentiality application: a view from the NIH Institutes

Author

Bernard Lo, Jolanta Zandecki, and Leslie E. Wolf

Subjects
Genetic Research, Health (social science), Human rights, business.industry, Research Subjects, media_common.quotation_subject, Data Collection, Internet privacy, Records, Certificate, Research Personnel, United States, Consent Forms, Human Experimentation, National Institutes of Health (U.S.), Environmental health, Government Regulation, Humans, Confidentiality, Guideline Adherence, Psychology, business, media_common, Behavioral Research
Published
2004

21. What must research subjects be told regarding the results of completed randomized trials?

Author

Maurie Markman

Subjects
medicine.medical_specialty, Health (social science), Paclitaxel, Research Subjects, Decision Making, Alternative medicine, Disclosure, law.invention, Consolidation therapy, Randomized controlled trial, law, medicine, Humans, Randomized Controlled Trials as Topic, Ovarian Neoplasms, Medical education, Advanced ovarian cancer, Informed Consent, Interpretation (philosophy), Principal (computer security), Subject (documents), Ethical conflict, Survival Analysis, Research Personnel, Paternalism, Treatment Outcome, Research Design, Female, Psychology, Ethics Committees, Research
Abstract

Federal research regulations require investigators to inform research subjects of "significant new findings developed during the course of the research which may relate to the subject's willingness to continue participation."1 However, the determination of what is, and what is not, relevant to disclose is open to interpretation and potential ethical conflict. The recently reported results of a multi-center randomized Phase III trial (in which the author of this commentary was the principal investigator) examining "maintenance/consolidation therapy" of advanced ovarian cancer provide a poignant example of the complexity of this fundamental issue."

Published
2004

22. Improving informed consent: a comparison of four consent tools

Author

Patricia, Agre and Bruce, Rapkin

Subjects
Clinical Trials as Topic, Internationality, Vietnam, Neoplasms, Humans, Guidelines as Topic, Curriculum, Developing Countries, Research Personnel, United States, Ethics, Research, Social Control, Formal
Published
2004

24. Barriers encountered conducting informed consent research

Author

Patricia, Agre, Bruce, Rapkin, James, Dougherty, and Roger, Wilson

Subjects
Health Knowledge, Attitudes, Practice, Human Experimentation, Informed Consent, Time Factors, Research Design, Research Subjects, Humans, Research Personnel
Published
2003

25. Lawsuits target medical research

Author

Alice Dembner

Subjects
medicine.medical_specialty, Clinical Trials as Topic, Health (social science), Informed Consent, Research Subjects, Liability, Malpractice, Ethics committee, MEDLINE, Liability, Legal, Medical research, Research Personnel, Human Experimentation, Informed consent, Family medicine, Political science, medicine, Humans, Stress, Psychological, Ethics Committees, Research
Published
2003

27. Expanding disclosure of conflicts of interest: the views of stakeholders

Author

Baruch A, Brody, Cheryl, Anderson, S Van, McCrary, Laurence, McCullough, Robert, Morgan, and B A, Brody

Subjects
Clinical Trials as Topic, Biomedical Research, Time Factors, Conflict of Interest, Research Subjects, Data Collection, Administrative Personnel, Disclosure, Organizational Policy, Research Personnel, United States, Attitude, National Institutes of Health (U.S.), Ethicists, Research Support as Topic, Surveys and Questionnaires, Humans, Periodicals as Topic, Editorial Policies, Ethics Committees, Research
Published
2003

28. Managing financial conflicts of interest

Subjects
Clinical Trials as Topic, Biomedical Research, Conflict of Interest, Research Support as Topic, Humans, Industry, Empirical Research, Organizational Policy, Research Personnel
Published
2003

29. Ethical oversight of research in developing countries

Author

Nancy, Kass, Liza, Dawson, and Nilsa I, Loyo-Berrios

Subjects
Risk, Clinical Trials as Topic, Health Knowledge, Attitudes, Practice, Informed Consent, Internationality, Universities, Advisory Committees, Guidelines as Topic, Focus Groups, Research Personnel, United States, Ethics, Research, Consent Forms, Human Experimentation, Government, Government Regulation, Humans, Health Services Research, Ethical Review, Developing Countries, Behavioral Research, Ethics Committees, Research
Published
2003

30. Ten questions institutional review boards should ask when reviewing international clinical research protocols

Author

Daniel W, Fitzgerald, Angela, Wasunna, and Jean William, Pape

Subjects
Clinical Trials as Topic, Social Responsibility, Informed Consent, Internationality, Research Subjects, Interprofessional Relations, Health Services Accessibility, Research Personnel, Ethics, Research, Human Experimentation, Research Design, Humans, Public Health, Comprehension, Ethical Review, Developing Countries, Ethics Committees, Research
Published
2003

31. The right of subjects to see the protocol

Author

Robert M, Veatch

Subjects
Informed Consent, Research Subjects, Vaccination, Disclosure, Middle Aged, Herpes Zoster, Risk Assessment, Research Personnel, United States, Access to Information, Consent Forms, Chickenpox, Human Experimentation, Patient Rights, Attitude, Clinical Protocols, National Institutes of Health (U.S.), Research Design, Humans, Randomized Controlled Trials as Topic
Published
2003

32. Informed consent for Alzheimer's disease clinical trials: a survey of clinical investigators

Author

Jason H T, Karlawish, David, Knopman, Christopher M, Clark, John C, Morris, Daniel, Marson, Peter J, Whitehouse, and Claudia H, Kawas

Subjects
Clinical Trials as Topic, Health Knowledge, Attitudes, Practice, Informed Consent, Research Subjects, Data Collection, Patient Selection, Proxy, Research Personnel, United States, Consent Forms, Alzheimer Disease, Government Regulation, Humans, Mental Competency, Third-Party Consent, Ethics Committees, Research, State Government
Published
2003

34. Integrating research ethics and undercover hospital fieldwork

Author

Chris Herrera

Subjects
Research ethics, Health (social science), Deception, Informed Consent, business.industry, Hospitals, Research Personnel, Ethics, Research, Human Experimentation, Research Design, Medicine, Humans, Engineering ethics, Health Services Research, business, Professional Misconduct, Behavioral Research, Ethics Committees, Research
Published
2003

35. Research ethics and the 'fieldwork monitoring committee'

Author

Chris Herrera

Subjects
Adult, Risk, Research ethics, Health (social science), Substance-Related Disorders, Advisory Committees, Research Personnel, Ethics, Professional, Political science, Humans, Engineering ethics, Ethical Review, Anthropology, Cultural, Behavioral Research, Ethics Committees, Research
Published
2002

36. IRB review of adverse events in investigational drug studies

Author

Ernest D, Prentice and Bruce, Gordon

Subjects
Ethics, Risk, Ethics Committees, Informed Consent, Drug-Related Side Effects and Adverse Reactions, Research Subjects, United States Food and Drug Administration, Cost-Benefit Analysis, Federal Government, Drugs, Investigational, Mandatory Reporting, Risk Assessment, Research Personnel, United States, Social Control, Formal, Consent Forms, Human Experimentation, Government, Government Regulation, Humans, Ethical Review, Ethics Committees, Research
Published
2001

37. A case study in adolescent participation in clinical research: eleven clinical sites, one common protocol, and eleven IRBs

Author

Gloria Weissman, Audrey Smith Rogers, Donald F Schwartz, and Abigail English

Subjects
Risk, medicine.medical_specialty, Health (social science), Adolescent, Research Subjects, Sexually Transmitted Diseases, HIV Seropositivity, medicine, Humans, Multicenter Studies as Topic, Parental Consent, Ethical Review, Third-Party Consent, Protocol (science), Ethics, Ethics Committees, Data Collection, Control Groups, Research Personnel, United States, Clinical research, Human Experimentation, Evaluation Studies as Topic, Research Design, Family medicine, Psychology, Confidentiality, Ethics Committees, Research
Published
2001

38. A reappraisal of female adolescent participation in drug clinical trials

Author

Terry M, VandenBosch, Becky G, Ward, and Debra, Mattison

Subjects
Freedom, Risk, Health Knowledge, Attitudes, Practice, Adolescent, Research Subjects, Federal Government, Social Justice, Humans, Parental Consent, Women, Third-Party Consent, Clinical Trials as Topic, Communication, Patient Selection, Research, Beneficence, Reference Standards, Altruism, Therapeutic Human Experimentation, Research Personnel, United States, Social Control, Formal, Paternalism, Contraception, Human Experimentation, Research Design, Government, Personal Autonomy, Government Regulation, Female, Sexuality, Stress, Psychological
Published
2001

39. A relational perspective on ethics-in-science decisionmaking for research with vulnerable populations

Author

Celia B, Fisher

Subjects
Freedom, Moral Obligations, Risk, Adolescent, Research Subjects, Decision Making, Persons with Mental Disabilities, Federal Government, Guidelines as Topic, Public Policy, Disclosure, Risk Assessment, Vulnerable Populations, Researcher-Subject Relations, Social Justice, Humans, Third-Party Consent, Social Responsibility, Informed Consent, Research, Beneficence, Altruism, Research Personnel, United States, Persons, Social Control, Formal, Human Experimentation, Attitude, Socioeconomic Factors, Government, Personal Autonomy, Government Regulation, Empathy, Confidentiality, Behavioral Research
Published
2001

41. Protocol review within the context of a research program

Author

Franklin G, Miller and Donald L, Rosenstein

Subjects
Risk, Volunteers, Patients, Research Subjects, Coercion, Disclosure, Risk Assessment, Consent Forms, Placebos, Cognition, Patient Education as Topic, Physicians, Humans, Ethical Review, Ethics, Information Services, Ethics Committees, Motivation, Informed Consent, Information Dissemination, Research, Therapeutic Human Experimentation, Nontherapeutic Human Experimentation, Research Personnel, Human Experimentation, Research Design, Comprehension, Ethics Committees, Research
Published
2001

42. 'There is no substantive due process right to conduct human-subject research': the saga of the Minnesota Gamma Hydroxybutyrate Study

Author

Dale E, Hammerschmidt

Subjects
Ethics, Ethics Committees, Jurisprudence, Informed Consent, Universities, Judicial Role, Research Subjects, Substance-Related Disorders, Scientific Misconduct, Liability, Legal, Drugs, Investigational, Research Personnel, Human Experimentation, Punishment, Civil Rights, Humans, Ethical Review, Ethics Committees, Research
Published
1997

43. Ethical guidelines for rTMS research

Author

Ronald M, Green, Alvaro, Pascual-Leone, and Eric M, Wasserman

Subjects
Risk, Volunteers, Depressive Disorder, Informed Consent, Internationality, Databases, Factual, Patients, Research Subjects, International Cooperation, Patient Selection, Research, Guidelines as Topic, Reference Standards, Risk Assessment, Therapeutic Human Experimentation, Electric Stimulation, Nontherapeutic Human Experimentation, Research Personnel, Human Experimentation, Evaluation Studies as Topic, Methods, Humans, Registries
Published
1997

44. Continuing review of research involving human subjects: approach to the problem and remaining areas of concern

Author

Bruce, Gordon and Ernest, Prentice

Subjects
Ethics, Risk, Ethics Committees, Time Factors, Universities, Research Subjects, United States Food and Drug Administration, Patient Selection, Records, Federal Government, Guidelines as Topic, Reference Standards, Risk Assessment, Research Personnel, United States, Social Control, Formal, Human Experimentation, Research Design, Government, Government Regulation, Humans, Multicenter Studies as Topic, Ethical Review, Ethics Committees, Research
Published
1997

45. Collaborative research involving human subjects: a survey of researchers using international single project assurances

Author

Deloris Mills, Janet Smith, Alison Wichman, and Alan L. Sandler

Subjects
medicine.medical_specialty, Health (social science), Internationality, Time Factors, Social Values, International Cooperation, education, Federal Government, Guidelines as Topic, Acquired immunodeficiency syndrome (AIDS), Political science, Surveys and Questionnaires, medicine, Humans, Developing Countries, Medical education, Ethics Committees, Public health, Communication, Data Collection, Cultural Diversity, medicine.disease, Research Personnel, United States, Social Control, Formal, Clinical research, Human Experimentation, Attitude, National Institutes of Health (U.S.), Multinational corporation, Evaluation Studies as Topic, Government, Government Regulation, Engineering ethics, Human research, Malaria, Ethics Committees, Research
Abstract

much suffering, and death, for many people throughout the world. The Acquired Immunodeficiency Syndrome, malaria, dysentery, nutritional and vitamin-deficiency disorders, a host of infectious diseases, many public health issues, and the effects on humans of exposure to radiation, are under intense study by teams of multinational researchers. As a result of the expansion of international collaborative clinical research, increased attention is being directed to the protection of human research subjects. This interest has been stimulated, in part, by a general agreement among researchers, ethicists, public policymakers, and others

Published
1997

47. Psychology faculty satisfaction and compliance with IRB procedures

Author

Becky J, Liddle and Elizabeth W, Brazelton

Subjects
Ethics Committees, Health Knowledge, Attitudes, Practice, Time Factors, Universities, Data Collection, Research, Social Control, Informal, Faculty, Research Personnel, United States, Attitude, Evaluation Studies as Topic, Humans, Psychology, Professional Autonomy, Behavioral Research, Ethics Committees, Research
Published
1996

48. The Prussian regulation of 1900: early ethical standards for human experimentation in Germany

Author

Jochen, Vollmann and Albert, Neisser

Subjects
Freedom, History, Jurisprudence, Informed Consent, Research Subjects, Scientific Misconduct, Guidelines as Topic, History, 19th Century, History, 20th Century, Hospitals, Nontherapeutic Human Experimentation, Research Personnel, Social Control, Formal, Human Experimentation, Germany, Physicians, Personal Autonomy, Government Regulation, Humans
Published
1996

49. Structuring the review of human genetics protocols: gene localization and identification studies

Author

Kathleen Cranley, Glass, Charles, Weijer, Roberta M, Palmour, Stanley H, Shapiro, Trudo M, Lemmens, and Karen, Lebacqz

Subjects
Freedom, Moral Obligations, Risk, Genetic Research, Research Subjects, Coercion, Genetic Counseling, Guidelines as Topic, Disclosure, Truth Disclosure, Risk Assessment, Terminology as Topic, Genetics, Methods, Humans, Family, Social Change, Ethical Review, Genetic Privacy, Probability, Ethics, Ethics Committees, Social Responsibility, Informed Consent, Conflict of Interest, Patient Selection, Uncertainty, Research Personnel, United States, Pedigree, Human Experimentation, Research Design, Personal Autonomy, Confidentiality, Ethics Committees, Research
Published
1996

50. Exempt research: procedures in the intramural research program of the National Institutes of Health

Author

Alan L. Sandler, Deloris Mills, and Alison Wichman

Subjects
Ethics, Research program, Ethics Committees, Health (social science), business.industry, Records, Federal Government, Social Control, Informal, Public relations, Public administration, Research Personnel, United States, Social Control, Formal, Human Experimentation, National Institutes of Health (U.S.), Political science, Government, Government Regulation, Humans, Forms and Records Control, business, Ethical Review, Ethics Committees, Research
Published
1996

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