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High vs. Standard Dose Flu Vaccine in Adult Stem Cell Transplant Recipients: DID Protocol Number 170085 Protocol version 6.0 NCT03179761 Date: August 12, 2019 NCT03179761High vs. Standard Dose Flu
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How to fill out a double-blind randomized trial

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How to fill out a double-blind randomized trial

01
Select participants randomly and assign them to either the control group or the treatment group.
02
Make sure that neither the participants nor the researchers know which group each participant has been assigned to.
03
Administer the treatment to the treatment group and a placebo or standard treatment to the control group.
04
Collect data on the outcomes of interest in a way that does not reveal which group each participant belongs to.
05
Analyze the data in a way that preserves the blindness of the study design.

Who needs a double-blind randomized trial?

01
Researchers conducting clinical trials to evaluate the effectiveness of a new treatment or intervention.
02
Regulatory agencies like the FDA that require high-quality evidence before approving new drugs or medical devices.
03
Healthcare providers who want to make evidence-based decisions about which treatments to recommend to their patients.
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A double-blind randomized trial is a type of study where neither the participants nor the researchers know who is receiving the treatment and who is receiving the placebo.
Researchers conducting clinical trials are required to file a double-blind randomized trial.
To fill out a double-blind randomized trial, researchers need to carefully design the study, recruit participants, randomly assign treatments, and collect and analyze data without knowing the treatment assignments.
The purpose of a double-blind randomized trial is to minimize bias and accurately assess the effectiveness of a treatment.
A double-blind randomized trial must report detailed information on study design, participant demographics, treatments received, outcomes measured, and statistical analysis.
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