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Pages:
1 page/β‰ˆ275 words
Sources:
3 Sources
Style:
APA
Subject:
Social Sciences
Type:
Essay
Language:
English (U.S.)
Document:
MS Word
Date:
Total cost:
$ 4.32
Topic:

Concerns that Participants in Human Subjects Express and the Usual Process Addressing Them

Essay Instructions:

Alternative Assignment
1. Find at least two scholarly references that address the following questions. You may need more references if the two you find do not address all questions. Scholarly articles are articles that are peer reviewed and can be found in professional journals. Most sources found on CINAHL are scholarly sources. Another place to look is Google Scholar.
2. Write an essay of 250 to 300 words that addresses the following questions. The word limit is for the body of the essay, not counting references. Be sure to use APA format. You may not use personal pronouns such as “I” or “my”. Use a 7th edition APA cover page. You can follow the sample cover page for the Finding the Evidence paper as a model. You can title your paper “Alternative Research Assignment”. THESE ARE THE QUESTIONS TO ANSWER...
A. What are concerns that participants in human subjects studies frequently express?
B. What is the usual process for addressing those concerns? How well does this process work?
C. What are potential triggers for participants? How can those triggers be addressed?
D. How well do participants think their rights are protected?

Essay Sample Content Preview:

Alternative Research Assignment
Student's Name
Institutional Affiliation
Instructor
Date
Concerns that Participants in Human Subjects Express
A human subject is a living individual whom a medical student or professional researches. The study is conducted by obtaining information or biospecimens by interacting with the personnel to analyze and generate identifiable private information. Participation of human subjects in biomedical research implicates various ethical concerns in terms of values such as informed consent, bodily integrity, privacy, safety, dignity, and autonomy (Resnik, 2019).
The Usual Process for Addressing the Concerns
During biomedical research, medical investigators are responsible for observing ethical considerations to minimize harm and preserve respect for human subjects. In this regard, Institutional Review Boards were formulated to guarantee participant safety and protect their privacy and personal data (Lapid et al., 2019). According to FDA, any activity involving human subjects requires authorization from IRB to handle ethical concerns.
Potential Triggers for Human Participants
All medical researchers must correctly identify, disclose, and minimize any p...
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