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    Pragmatic Randomized Clinical Trials

    Pragmatic Randomized Clinical Trials

    - Using Primary Data Collection and Electronic Health Records

    Forfatter: info mangler
    Bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Pragmatic Randomized Clinical Trials Using Primary Data Collection and Electronic Health Records addresses the practical aspects and challenges of the design, implementation, and dissemination of pragmatic randomized trials, also sometimes referred to as practical or hybrid randomized trials. While less restrictive and more generalizable than traditional randomized controlled trials, such trials have specific challenges which are addressed in this book. The book contains chapters encompassing common designs along with advantages and limitations of such designs, analytic aspects in planning trials and estimating sample size, and how to use patient partners to help design and operationalize pragmatic randomized trials. Pragmatic trials conducted using primary data collection and trials embedded in electronic health records - including electronic medical records and administrative insurance claims - are addressed.This comprehensive resource is valuable not only for pharmacoepidemiologists, biostatisticians and clinical researchers, but also across the biomedical field for those who are interested in applying pragmatic randomized clinical trials in their research.

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    Detaljer
    • SprogEngelsk
    • Sidetal498
    • Udgivelsesdato14-04-2021
    • ISBN139780128176634
    • Forlag Academic Press Inc
    • FormatPaperback
    Størrelse og vægt
  • Vægt1040 g
    • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Implant Incarceration Community Schizophrenia Future Engagement Fidelity Clinical trials Epidemiology Informed Consent. Replication Data processing Effectiveness Patients Hypothesis Pharmacoepidemiology Selection Natural language processing Validation Bias Comparative Effectiveness Research Electronic Health Records Implementation Consensus Biological Real-world Missing data Pragmatic Trials Confounding Reproducibility Selection bias Competing Risk Stakeholder engagement Reimbursement Decision maker Behavioral economics Research Ethics Dissemination RCT EHR Adherence Medical practice Representativeness Algorithm Diagnostic Pragmatic Heterogeneity Stakeholders Linkage Unstructured Data Rare disease Mobile App Outcomes Research Electronic Health Record Regulatory Randomization Medical device Human subjects Patient-Centered Data quality Sensitivity analysis Efficacy Adjudication Patient engagement Research question Blinding Précis Misclassification Payer Administrative Claims Data Bias analysis Biologics and biosimilars collective intelligence consortium Choice of design and analytic approaches Common data model Distributed research network Centralized data approach Distributed programming approach Claims data Computable phenotype Control conditions Goal of pragmatism Free text FDA-catalyst Implementation latent characteristics Distributed protocol approach Hybrid trial Injectable antipsychotic medications Explanatory clinical trials Massachusetts all-payers claims database Methods guidelines NIH health care systems research collaboratory Paliperidone Palmitate Health care systems research network Outcome validation Patient perspectives Pragmatic clinical trial Pragmatic trials (pRCTs)Masking PRECIS-2Primary data collection Observational health data sciences and informatics Real world data (RWD)Feasibility assessment Patient-centered outcomes research network Payers IMPACT-AFib Pragmatic randomized clinical trial Pragmatic trial design Privacy-preserving analytics Information Bias Pragmatic clinical trials Registry-based randomized trial Stepped wedge cluster randomized trials (SW-CRT)Transparency Registry-embedded trials statistical assumptions Informative censoring NIH's all of us Operational definitions Reporting guidelines PFMD RWE framework Quantitative bias analysis Sentinel system
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