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Dec 6, 2023

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ETHICS AND RESEARCH STUDY Quiensala Hamilton HCS/435 Yvette Mallory 10/23/2023
Content WHAT IS INFORMAL/BR OAD CONSENT WHAT IS INFORMAL/BR OAD CONSENT ETHICAL CONCERNS ETHICAL CONCERNS IMPACT OF EVIDENCE- BASED RESEARCH IMPACT OF EVIDENCE- BASED RESEARCH WHY RESEARCH STUDIES VS QMP WHY RESEARCH STUDIES VS QMP EXTERNAL FACTORS THAT IMPACT ETHICAL CONCERNS EXTERNAL FACTORS THAT IMPACT ETHICAL CONCERNS RELATIONSHIP BETWEEN ETHICS AND COLLECTING DNA RELATIONSHIP BETWEEN ETHICS AND COLLECTING DNA RELATIONSHIP BETWEEN ETHICS AND COLLECTING DNA RELATIONSHIP BETWEEN ETHICS AND COLLECTING DNA
What is Formal Consent in Research Informed consent is a legal and ethical requirement Participants must be informed. This ensure that human participants are protected. This means that the person…should have sufficient knowledge and comprehension of the elements of the subject matter involved, as to enable him to make an understanding and enlightened decision. This latter element requires that, before the acceptance of an affirmative decision by the experimental subject, there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person, which may possibly come from his participation in the experiment.
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Important Elements of Informed Consent Information Sharing 1 1 Comprehension 2 2 Voluntariness 3 3 Decision-Making Ability 4 4
ETHICAL CONCERNS A set of guidelines that direct research ideas and procedure are know as ethical considerations There is a code of conduct that researchers must always follow when gathering information from participants
EVIDENCE- BASED RESEARCH Impact the creation of guidelines• Ensures that the patient is the major focus; Encourages higher quality standards; • Provides a solid foundation of knowledge for the patient Click icon to add picture
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Evidence-Based research . Clinical Expertise Best Research Evidence Patient Values of Preferences
Eliminating or Minimizing Ethical Concerns in the Healthcare Industry with Evidence-Based research .
Research Studies and Quality Management Regulatory Research studies seeks information to prove effectiveness Measures the effect of single intervention Gathers information about a particular topic Has several process and can be a lengthy process Quality management seeks improvement information for better patient care such as policy’s investigate the process of continuous improvement and its long-term viability. Evaluates adverse events patient outcomes and experience Faster process to improving patient care
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External Factors That Have an Impact on The Ethical Concern Study Purpose Goals that the researcher is aiming for Confidentiality How will the participant information will be used
Relationship Between Ethics and Healthcare Research Informed consent Genetic and Genomic Research Test Protection Maintaining Privacy and Confidentiality of Genetic information Preventing Genetic Discrimination
Conclusion We've discussed the value of informed consent and the critical role ethics play in research. Since healthcare is evolving, informed consent has also changed. It's critical to stay informed about legislative changes and comprehend what ethical behavior means when conducting research. The one-time or continuous use of samples necessitates an understanding of the ethical influence on informed consent. Numerous mechanisms exist to assist researchers in obtaining informed consent while preventing violations and participant damage. The research has an obligation to do no harm. Assessing research participants in accordance with current standards and with respect is one of the most crucial things to do. Ultimately, the position of a researcher also includes a social obligation to make sure that their study advances patient care quality, benefits society,
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