Posted: April 25th, 2022
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Formulate an approach to the recruitment and consent process for your research study. The study: randomized clinical trial looking at the effectiveness of cannabis to treat neuropathic pain. Using the required resources as a guide, demonstrate a strategy for protecting vulnerable participants and identifying anticipated ethical issues that may arise in your study design. Include answers to the following prompts in your submission: – What is your target study population? – What vulnerabilities does your population face? (examples: pediatric patients, medical frailty, cognitive impairment, low health literacy, financial challenges, environmental challenges, risks of adverse outcomes, etc) -What are the potential risks to participants in your study? – Will your study design and methodology require IRB review and approval? Explain why or why not. – How will you optimize participant comprehension in your informed consent process? – What methods will you use to protect the private health information and confidentiality of participants? – Name two possible consequences of investigator misconduct in your study. Use AMA format
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