Informed consent for pragmatic trials--the integrated consent model.
about
Stakeholders' views on the ethical challenges of pragmatic trials investigating pharmaceutical drugs.The Comprehensive Post-Acute Stroke Services (COMPASS) study: design and methods for a cluster-randomized pragmatic trial."Targeted" consent for pragmatic clinical trialsCan an antimicrobial stewardship program reduce length of stay of immune-competent adult patients admitted to hospital with diagnosis of community-acquired pneumonia? Study protocol for pragmatic controlled non-randomized clinical study.Harms, benefits, and the nature of interventions in pragmatic clinical trials.Ethical complexities in standard of care randomized trials: A case study of morning versus nighttime dosing of blood pressure drugsUse of altered informed consent in pragmatic clinical research.Involving patients in enrolment decisions for acute myocardial infarction trialsTrends in Consent for Clinical Trials in Cardiovascular Disease.Registry-Based Pragmatic Trials in Heart Failure: Current Experience and Future Directions.Anticipated Ethics and Regulatory Challenges in PCORnet: The National Patient-Centered Clinical Research Network.Pragmatic Randomized Trials Without Standard Informed Consent?: A National Survey.Public preferences on written informed consent for low-risk pragmatic clinical trials in Spain.Targeted Consent for Research on Standard of Care Interventions in the Emergency Setting.A comparison of institutional review board professionals' and patients' views on consent for research on medical practices.Proposals to Conduct Randomized Controlled Trials Without Informed Consent: a Narrative Review.Who is willing to participate in low-risk pragmatic clinical trials without consent?Enhancing accrual to chemotherapy trials for patients with early stage triple-negative breast cancer: a survey of physicians and patients.Patients' beliefs regarding informed consent for low-risk pragmatic trials.Commentary on Kim Miller.Willingness to participate in pragmatic dialysis trials: the importance of physician decisional autonomy and consent approach.Routinely collected data for randomized trials: promises, barriers, and implications.Is it important to disclose how treatments are selected in clinical research and clinical care?What's new in ethics of cardio-pulmonary resuscitation research: too little time and too many rules?A multi-center pragmatic, randomized, feasibility trial comparing standard of care schedules of filgrastim administration for primary febrile neutropenia prophylaxis in early-stage breast cancer.Does Consent Form Follow Function?Reframing Consent for Clinical Research: A Function-Based Approach.The Transition to Precision Psychiatry and Pragmatic Inquiry Methods in Academic Psychiatry: The Example of Point-of-Care Clinical Trials.Ethical issues in pragmatic randomized controlled trials: a review of the recent literature identifies gaps in ethical argumentation.When and Why Is Research without Consent Permissible?Commentary on Wilson et al.When and how should we cluster and cross over: methodological and ethical issues.Ensuring respect for persons in COMPASS: a cluster randomised pragmatic clinical trialThe patient's perspective on the need for informed consent for minimal risk studies: Development of a survey-based measure
P2860
Q27332116-2CADBB56-1ECA-4A7D-9FBA-241442C4767AQ33909494-E4E490AD-722D-4F5E-A9B5-B4331E95FED0Q35396652-8F120354-601B-4FAA-BAED-B296D8A1FE40Q35949538-1479F1D7-B047-494E-9E90-26DE9A66FB99Q36117803-E7D27586-CFE5-4A50-8663-429439B3CAEDQ36275898-9EB5A60E-CB9B-4503-95FC-64522910F104Q36397913-ABF23BF1-7787-49F8-94BC-CAF9EEBD3E6BQ36448976-C83F604F-D51E-461E-973D-ED07E10F2FA1Q37076220-447B92D6-C39D-4FEC-B76E-DB27ACE1E07DQ37710165-0F6DC1C3-7695-4D91-B4E5-4ABCDC7BC131Q38550799-4FFD099D-CB4D-4205-BAF8-AAADE89B1CF1Q38555205-F389D639-1EF9-43A2-B38E-75E97177CB27Q38832151-D1772919-4FD9-4A76-8182-067355F875CFQ38832678-FC61117B-DADA-4236-A8CB-E472630C379BQ38852440-B1BDF1B4-CE12-4E17-9265-17BBB2006A4CQ38888145-6AAE1ECD-4748-455A-AA06-41CFD23CCE45Q40044320-E014A83E-0F40-4036-8210-96DE4C894F5CQ40362543-C7B3F4D3-C663-4DA2-B601-85C55BD3B727Q41711995-FC731462-AAA6-4448-B560-35264B7E0BA3Q41837685-B1110E36-146C-4992-B7CB-1EDD83EAA842Q42375084-435F9A81-2E60-4387-BFA3-D906591635A8Q47547328-0320AFB3-33B9-4318-9023-BC36D93F6336Q47928731-BF7B853C-D636-4FA7-98D5-389768F12571Q48059231-433FC9CF-E759-4526-9898-78A5232A4CFEQ48163223-AABCAF18-E22D-45A6-9119-DA99A54C448FQ48282337-E7908BBD-5116-4EC4-ABF0-DD5B9F9EC531Q49923167-9E19D783-C052-42A3-89F7-212BA224260FQ50037046-E59955E0-58F4-4417-9DC9-69C8ACB26962Q50354508-27AEE155-C19D-4A07-9B37-EB46CF278C11Q51511583-7CE1D7D5-B85A-494C-8F89-E7C2AA913383Q51794224-A1F2699C-E0DF-4561-975E-3E014993A987Q55282467-C19044A7-75D1-4075-95B1-C3DD48006F23Q56524643-1B74B488-39C2-47C5-9C88-6B48044AA466Q58266415-F8D063DB-BF31-421C-BDC2-E3928B6212DB
P2860
Informed consent for pragmatic trials--the integrated consent model.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Informed consent for pragmatic trials--the integrated consent model.
@en
Informed consent for pragmatic trials--the integrated consent model.
@nl
type
label
Informed consent for pragmatic trials--the integrated consent model.
@en
Informed consent for pragmatic trials--the integrated consent model.
@nl
prefLabel
Informed consent for pragmatic trials--the integrated consent model.
@en
Informed consent for pragmatic trials--the integrated consent model.
@nl
P356
P1476
Informed consent for pragmatic trials--the integrated consent model.
@en
P2093
Franklin G Miller
Scott Y H Kim
P304
P356
10.1056/NEJMHLE1312508
P407
P577
2014-02-01T00:00:00Z