M3 A6 WA: HUMAN SUBJECTS RESEARCH PROTECTION

M3 A6 WA: INSTRUCTIONS – HUMAN SUBJECTS RESEARCH PROTECTION

Content

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Overview

This assessment requires you to visit the The Research Clinic:

https://ori.hhs.gov/TheResearchClinicVideo/

You will click to play Jan Klein, RN. Work your way through the brief videos, choosing the best response as the RN assisting in research.

Upon completing the videos, you will submit a Word file that summarizes the essential elements of informed consent, special populations that require special legal and ethical research considerations, and the nurse’s role in advocating for the patient in research situations.

Your summary should be between 200-300 words. Provide a minimum of 2 references, in APA format, supporting your summary.

| GET AN EXPERT FOR YOUR ASSIGNMENT /

Objectives

• Understand the history behind the development of Human Subjects Protection guidelines
• To identify and describe the three principles of ethical human subjects research identified in the Belmont Report
• To identify risks associated with participation in research and appropriate protections against risks, vulnerable populations that need specific protections, and situations in which research involving humans is exempt from regulatory requirements
• Identify the essential elements of an informed consent form
• Describe the nurse’s role as patient advocate in research situations

Due Date: Sun, Feb 7 by 11:59 p.m. Eastern Standard Time (EST) of the US.

Point Value: 30

Instructions

To be successful, complete the following steps in order:

STEP 1. Review the overview and objectives.

STEP 2. Click here to download the rubric

STEP 3. Complete the web based course, “The Research Clinic”, playing the role of Jan Klein, RN

STEP 4. Create a word document, summarizing the essential elements of informed consent, special populations that require special legal and ethical research considerations, and the nurse’s role in advocating for the patient in research situations. Also, provide 2 references to support your summary. Your summary should be between 200-300 words.

STEP 5. Save the filename: “Lastname_Firstname_Module_3_Assessment_6” (Example: Smith_Jill_Module_3_Assessment_6)

STEP 6. Submit documents by clicking the link on the left titled “M3 A6 WA: SUBMISSION AREA – HUMAN SUBJECTS RESEARCH PROTECTION”

SAMPLE SOLUTION

One of the most important roles of a nurse is to be an advocate for the patient. Ensuring that the safety of human subjects involved in research is critical and therefore obtaining informed consent is a priority | GET AN EXPERT FOR YOUR ASSIGNMENT / exercise is to summarize important elements of informed consent, give special populations requiring special legal and ethical research considerations, and the role of the nurse in advocating for the patient in clinical research.
Informed consent is mandatory for all clinical trials that involve | GET AN EXPERT FOR YOUR ASSIGNMENT / of informed consent are disclosing full information, decision-making capacity of the patient or surrogate, and voluntarism (Miracle, 2016). Some of the information that the nurse has to disclose to the patient include but not limited to the purpose of the study, the study treatments or interventions and experimental procedures, potential risks and benefits from participating in the research, and the right to withdraw…