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Media preprint DOI: https://doi.org/10.1101/2020.10.15.20141457; this version posted October 20, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder,
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How to fill out a 12-month randomised double-blind
How to fill out a 12-month randomised double-blind
01
Obtain ethical approval for the study from the relevant committee.
02
Recruit participants who meet the eligibility criteria for the study.
03
Randomly assign participants to either the treatment group or the control group.
04
Ensure that neither the participants nor the investigators know who has been assigned to which group (double-blind).
05
Administer the treatment to the participants in the treatment group according to the study protocol.
06
Monitor and collect data on the participants throughout the 12-month study period.
07
Analyze the data at the end of the study to determine the effectiveness of the treatment.
Who needs a 12-month randomised double-blind?
01
Researchers conducting clinical trials to evaluate the effectiveness of a new treatment or intervention.
02
Drug companies seeking approval for new medications.
03
Medical professionals looking to determine the best course of treatment for their patients.
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What is a 12-month randomised double-blind?
A 12-month randomised double-blind study is a research trial in which participants are randomly assigned to receive either the experimental treatment or a placebo for a period of 12 months. Both the participants and the researchers are unaware of who is receiving the active treatment and who is receiving the placebo.
Who is required to file a 12-month randomised double-blind?
Researchers conducting clinical trials are typically required to file a 12-month randomised double-blind study protocol with regulatory authorities and ethics committees.
How to fill out a 12-month randomised double-blind?
To fill out a 12-month randomised double-blind study, researchers must carefully design the study protocol, obtain ethical approval, recruit participants, administer treatments, collect data, and analyze the results.
What is the purpose of a 12-month randomised double-blind?
The purpose of a 12-month randomised double-blind study is to evaluate the safety and efficacy of a new treatment over a 12-month period while minimizing bias and placebo effects.
What information must be reported on a 12-month randomised double-blind?
Researchers must report details of the study design, participant characteristics, treatment protocols, outcome measures, results, and statistical analysis in a 12-month randomised double-blind study.
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