When is informed consent required in cluster randomized trials in health research? - Wikidata - awgldk - TriplyDB

When is informed consent required in cluster randomized trials in health research?

When is informed consent required in cluster randomized trials in health research?

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Logistic, ethical, and political dimensions of stepped wedge trials: critical review and case studies A qualitative study exploring the acceptability of the McNulty-Zelen design for randomised controlled trials evaluating educational interventions SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials Effectiveness of a nutrition education package in improving feeding practices, dietary adequacy and growth of infants and young children in rural Tanzania: rationale, design and methods of a cluster randomised trial Restrictive vs liberal blood transfusion for acute upper gastrointestinal bleeding: rationale and protocol for a cluster randomized feasibility trial.Implementing evidence-based recommended practices for the management of patients with mild traumatic brain injuries in Australian emergency care departments: study protocol for a cluster randomised controlled trial Participant informed consent in cluster randomized trials: review.The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials.Early warning scoring systems versus standard observations charts for wards in South Africa: a cluster randomized controlled trial Ethical oversight in quality improvement and quality improvement research: new approaches to promote a learning health care system Ethical and regulatory issues of pragmatic cluster randomized trials in contemporary health systems.Exceptions to the rule of informed consent for research with an intervention.Personalized prescription feedback to reduce antibiotic overuse in primary care: rationale and design of a nationwide pragmatic randomized trial.What is the role and authority of gatekeepers in cluster randomized trials in health research?The ethics of testing a test: randomized trials of the health impact of diagnostic tests for infectious diseases.Reducing salt intake for prevention of cardiovascular diseases in high-risk patients by advanced health education intervention (RESIP-CVD study), Northern Thailand: study protocol for a cluster randomized trial.Researchers' perceptions of ethical challenges in cluster randomized trials: a qualitative analysis.Ethics Issues Arising in the Transition to Learning Health Care Systems: Results from Interviews with Leaders from 25 Health Systems Challenges for consent and community engagement in the conduct of cluster randomized trial among school children in low income settings: experiences from Kenya.Early intervention of patients at risk for acute respiratory failure and prolonged mechanical ventilation with a checklist aimed at the prevention of organ failure: protocol for a pragmatic stepped-wedged cluster trial of PROOFCheck Developing the ethics of implementation research in health.Variability in research ethics review of cluster randomized trials: a scenario-based survey in three countries.Challenges of cluster randomized trials.Cluster-randomized trials: A closer look.Inadequacy of ethical conduct and reporting of stepped wedge cluster randomized trials: Results from a systematic review.Response to Open Peer Commentaries on "Ethics of clinical science in a public health emergency: drug discovery at the bedside".Survey of consent practices in cluster randomized trials: improvements are needed in ethical conduct and reporting.Promoting deceased organ and tissue donation registration in family physician waiting rooms (RegisterNow-1 trial): study protocol for a pragmatic, stepped-wedge, cluster randomized controlled registry.Research to inform the consent-to-research process.Learning Health Care System: Pragmatic Comparison of Crystalloid Choice in a Medical Intensive Care Unit.Impact evaluation of a community engagement intervention in improving childhood immunization coverage: a cluster randomized controlled trial in Assam, India.

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When is informed consent required in cluster randomized trials in health research?

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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When is informed consent required in cluster randomized trials in health research?

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When is informed consent required in cluster randomized trials in health research?

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Allan Donner

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Andrew D McRae

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Angela White

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Ariella Binik

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Jamie C Brehaut

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Martin P Eccles

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Raphael Saginur

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P2860

Ethical issues in the design and conduct of cluster randomised controlled trials

Ethical issues in implementation research: a discussion of the problems in achieving informed consent.

Informed consent in school health research: why, how, and making it easy.

Equipoise and the ethics of clinical research.

Variations among Institutional Review Board reviews in a multisite health services research study.

Ethical issues posed by cluster randomized trials in health research.

Does clinical equipoise apply to cluster randomized trials in health research?

Who is the research subject in cluster randomized trials in health research?

Evidence for risk of bias in cluster randomised trials: review of recent trials published in three general medical journals.

International ethical guidelines for biomedical research involving human subjects.

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Jeremy Grimshaw

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