Website Link: Click on the following link to review one example of unethical research, this story reflects the Tuskegee Experiment.
https://www.history.com/news/the-infamous-40-year-tuskegee-study
Please review the videos below regarding research ethics.
Video: Research Ethics
https://www.youtube.com/embed/Zbi7nIbAuMQ?feature=oembed
Video: Ethics: Human Subject Research
https://www.youtube.com/embed/e0uydNe4cQo?feature=oembed
Video: How IRBs Protect Human Research Participants
https://www.youtube.com/embed/U8fme1boEbE?feature=oembed
Reading Reflection
Read Chapter 12:  Ethical Issues and Consent
Read Chapter 13: Participant Recruitment
Discussion Board Assignment
This week there are no formal discussion board assignments. However, I will request that everyone logs in to acknowledge that they have read both chapters 12 and 13.
Article Link: Institutional Review Boards – Purpose and Challenges
An IRB has the authority to approve, require modifications in (to secure approval), or disapprove research. This group review serves an important role in the protection of the rights and welfare of human research subjects.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631034/
Participant Recruitment for Research
There are several methods for obtaining participants for your studies. Please remember that not all your participants that are recruited will be eligible to participate in your research studies.  They may be excluded based on your criteria. A prime example would be if you are conducting a study involving Asian females, you would have to exclude European males from the study, this is based on criteria, not discrimination.
https://digital.ahrq.gov/ahrq-funded-projects/emerging-lessons/participant-recruitment-research
Sample Participant Informed Consent
The following link provides an example of a sample participant’s informed consent. Please note the components that are contained within. Many schools have their own version for the students to utilize in research. If this became a requirement in your research paper, this form would be included in the appendices section, following your reference section and would be included in your paper’s table of contents.
https://www.tcd.ie/swsp/assets/pdf/Participant%20consent%20form%20template.pdf
Take a moment to think about how you would incorporate the principles of ethics into your research. Would you willingly violate ethical principles to get your papers published or complete your studies?
How would you inform your participants regarding their rights? What would you do if you discover that a participant does not comprehend the terms of the agreement or has a language barrier? We are responsible for the well-being of our participants. This data must be included on your IRB initial application, also the methodology section of your papers much include this data.
It is also important for us to protect research data which must be secured both during and after the study. It is also our responsibility to inform the IRB that the study has been concluded and documents must be completed to reflect this change.

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