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Protocol & Statistical Analysis Plan for:Pragmatic Trial of COVID-19 Vaccine Text Outreach Interventions University of Pennsylvania Dr. Shiva Meta NCT#04834726 v. 11162021 Approved: 11192021Pragmatic
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01
Identify the research question and objectives of the pragmatic trial.
02
Develop the study protocol including eligibility criteria, intervention, outcome measures, and data collection methods.
03
Obtain ethical approval from relevant authorities.
04
Recruit participants based on the eligibility criteria.
05
Randomize participants to intervention groups as per the study protocol.
06
Implement the intervention according to the study protocol.
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Collect data on outcomes as specified in the protocol.
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Interpret the results and draw conclusions based on the findings.
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Publish the results in a peer-reviewed journal or share with the scientific community.

Who needs pragmatic trial of covid?

01
Researchers and scientists studying the efficacy and safety of interventions for COVID-19.
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Healthcare providers looking to implement evidence-based practices for treating COVID-19 patients.
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Policy makers and public health officials making decisions about COVID-19 prevention and control strategies.
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Patients and the general public interested in understanding the effectiveness of different treatments for COVID-19.
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A pragmatic trial of Covid is a research study that evaluates the effectiveness of interventions in real-world settings with real-world patients.
Researchers and organizations conducting clinical trials on Covid are required to file a pragmatic trial of Covid.
To fill out a pragmatic trial of Covid, researchers must report information about the study design, interventions, outcomes, and patient population.
The purpose of a pragmatic trial of Covid is to provide real-world evidence on the effectiveness of interventions in treating patients with Covid.
Researchers must report information about the study design, interventions, outcomes, patient population, and any adverse events.
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