APA Format
10 Pages (2750 Words)
Deadline July 18, 2019
NO PLAGIARISM
SAMPLE PAPER WILL BE PROVIDED
Select a healthcare related research study .
Identify the sample population.
Analyze and critique the study to identify if sampling method reflects ethical principles including consent, conditions of the participants, study approved by IRB.
Minimum 12 pages excluding title and reference page.
Introduction
Paragraph one is the introduction to the paper. It should begin with something that will grab the reader’s attention and provide a citation to support your opening sentence (Norwood, 2002). Next, support that opening sentence with discussion or explanation with one or multiple sentences which will make up the body of the introductory paragraph. The last sentence of the introduction should highlight areas to be covered in the paper. APA success requires knowledge of the format and skill in concise, clear written communication.
Research Study Overview
This section is where you provide a summary of the research study being critiqued? What were the goals of the research? What health care related issue was addressed? Is it a good/feasible study to apply in clinical practice? Was a practical study, from a financial aspect? Use as many paragraphs as needed to cover the content appropriately.
Ethical Issues in Research
Use this paragraph to provide feedback/history on ethical issues on research.
Protection of Human Rights
What are the five human rights that must be protected during research/investigation? What do they stand for? How do they relate to this research study? Were any/all of the human rights protected in the duration of the research study in question? Use as many paragraphs as needed to cover the content appropriately.
Sampling Method
What was the sampling method used, how did the researchers choose the subjects for participation? What other sampling methods could have worked better, provided better results? Does the sampling method used reflect ethical principles, was it a fair process? Is the population in question a vulnerable population, and if so were there special considerations taken? Use as many paragraphs as needed to cover the content appropriately.
Informed Consent
What is an informed consent? In regards to this research study, was it obtained, if appropriate? If a consent was part of the study, was it obtained properly? Did the participants assent? If participants unable to consent, were they not competent, did a caregiver consent? Were participants provided full/complete detailed information or was it a short version? What components did it include? Use as many paragraphs as needed to cover the content appropriately.
Ethical Scientific Integrity
What are the credentials of the researchers? Did the researchers fabricate data, publish errors/ publish correction? Is there evidence of plagiarism? Use as many paragraphs as needed to cover the content appropriately.
IRB
This section is where you will discuss all the information available (or lack thereof) regarding the IRB. Was the research study approved by an institutional review board? If not, why not? Was a research proposal submitted for approval by an IRB? Use as many paragraphs as needed to cover the content appropriately
HIPPA
What is HIPPA and how does it apply to a research study? Was the research conducted using database information, and if so, was the health information protected? How was it protected? Was any data de-identified? Were participants provided pseudonyms or assigned numbers? Use as many paragraphs as needed to cover the content appropriately.
Benefit to Risk Ratio
Discuss if a benefit to risk ratio was calculated and how? Did it provide am honest estimation? What is your opinion about the outcome of the study and the potential benefits? Can it have a positive impact on the individual, how about in the community? Use as many paragraphs as needed to cover the content appropriately.
Conclusion
Most papers should end with a conclusion or summary, which consists a short description of the key points of the paper. It should be concise and contain little or no detail. No matter how much space is left on the page, the References are always on the next page.
Expert Solution Preview
Introduction:
In this assignment, we will analyze and critique a healthcare-related research study. Our focus will be on the sample population and the ethical principles followed in the study, including consent, conditions of the participants, and approval by the Institutional Review Board (IRB). The objective is to evaluate if the sampling method used reflects ethical principles and if the study upholds the protection of human rights. Additionally, we will discuss the concept of informed consent, ethical scientific integrity, the role of the IRB, and the application of the Health Insurance Portability and Accountability Act (HIPAA) in the research study. Finally, we will assess the benefit to risk ratio and provide a conclusion summarizing our findings.
Research Study Overview:
The research study selected for analysis aimed to address a specific healthcare-related issue and had well-defined goals. The study design, methodology, and the outcomes obtained will be briefly presented. The feasibility and practicality of applying the study findings in clinical practice will also be evaluated, considering financial implications. This section will provide a comprehensive summary of the research study under scrutiny.
Ethical Issues in Research:
Ethical considerations play a crucial role in any research study. In this paragraph, we will highlight the historical context and significant ethical issues associated with research. This will give the reader an understanding of the importance of ethical principles in protecting participants’ rights and the integrity of scientific inquiry.
Protection of Human Rights:
Five fundamental human rights must be protected during research and investigation. These rights, which will be discussed and explained, are essential to ensure ethical conduct and participant well-being. We will analyze how these rights relate to the research study in question and evaluate if they were upheld throughout the study duration.
Sampling Method:
The sampling method used in a research study has a significant impact on the validity and generalizability of the findings. In this section, we will analyze the sampling method employed in the selected study, including how the researchers chose the subjects for participation. We will also explore alternative sampling methods and discuss if they could have potentially provided better results. Ethical considerations regarding the fairness of the sampling process and whether the study population included vulnerable individuals will be addressed.
Informed Consent:
Informed consent is a crucial ethical principle that ensures participants are fully aware of the specifics of the study and voluntarily agree to participate. In this section, we will define informed consent and assess if it was obtained appropriately in the research study under review. We will also examine if participants were provided with complete and detailed information and if any special considerations were taken for individuals unable to consent.
Ethical Scientific Integrity:
Maintaining ethical scientific integrity is vital to the credibility and validity of research findings. We will discuss the credentials of the researchers involved in the selected study and evaluate if any evidence of data fabrication, publishing errors, or plagiarism was found. This section will provide insights into the trustworthiness and reliability of the research study.
IRB:
The research study’s approval by an Institutional Review Board (IRB) is a crucial aspect of ethical research. We will discuss the availability and adequacy of information regarding the IRB’s involvement in the study under examination. This section will also explore whether a research proposal was submitted for IRB approval, and if not, the reasons behind it.
HIPAA:
The Health Insurance Portability and Accountability Act (HIPAA) safeguards individuals’ protected health information. In this paragraph, we will explain the relevance of HIPAA in a research study and evaluate if the study adhered to the HIPAA regulations. We will analyze the existence of any data de-identification measures, as well as the protection of participants’ health information throughout the study.
Benefit to Risk Ratio:
Assessing the benefit to risk ratio in a research study is essential to determine whether the potential benefits outweigh the potential harm or risks. We will discuss if a benefit to risk ratio was calculated and how it was determined. Furthermore, we will provide an opinion on the outcome of the study and its potential benefits for individuals and the community.
Conclusion:
In conclusion, this assignment thoroughly analyzed a healthcare-related research study, focusing on the sample population and the ethical principles followed. We examined the sampling method, obtained informed consent, evaluated ethical scientific integrity, and assessed the role of the IRB and HIPAA in the study. Additionally, we explored the benefit to risk ratio and provided a summary of our findings. Ethical considerations are crucial in research, and adherence to ethical principles ensures the protection of participants’ rights and the integrity of scientific inquiry.
