Assignment Task
Task
What are the risks/biases and how these could be overcome? (e.g. maybe the oncologist will show a preferential to administer drug D to patients with severe disease, so blinded approaches will be used) The use of tables/figures to illustrate the design/number/characteristics of samples (e.g. when proposing Clinical Trials) Is highly encouraged. Ethics Details of what information you will provide for participants (Participant Information Sheet), e.g. age. gender, socioeconomic status etc. How will you obtain consent (Consent Form), e.g. all participants will be provided a written form to sign off. How can participants withdraw? e.g. participants can withdraw at any time. How will you store and manage data? e.g. hard drives, notes, images etc. How will you anonymise data? e.g. use of codes for serum samples etc. How will you deal with GDPR? At which Institutional Ethics Board will you apply for ethical approval of the study? Future perspectives (- 200 words! What is the impact of the study on society (e.g. what will this project add to previous knowledge, which group(s) of patients/participants will benefit from this research, how can health professionals can use the findings from this research, will it help to set guidelines for the treatment of disease etc).
What the next steps will be after completion.
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