The Pros And Cons Of Informed Consent - 854 Words

Methods Participants There were a quantity of 126 participants randomly designated to be part of this study. From these 126 participants, 59 were male (47%) and 60 were female (48%) with 7 participants not providing their gender (5%). Ages ranging from a minimum of 17 to a maximum of 59 with a mean of 25.30 years (SD=8.77), while seven participant’s age information was missing. The sample population involved 30.2% Caucasian (N=38), 42.9% Hispanic (N=54), 1.6% Native Indian (N=2), 11.9 African American (N=15), 4.0 Asian American (N=5) and 6.3% reporting others (N=8). See Appendix A Materials and Procedure In the study, prior to being presented to the research material, potential participants were informed about the possible risks and†¦show more content†¦In part three, participants were asked to read a short paragraph about Anna, a high school student who is bullied. After reading, participants were presented with a series of 17 questions whose they completed using a scale from 1 to 6 with 1 being â€Å"strongly disagree† and 6 â€Å"strongly agree†. The last question of part three were to reminisce what they wrote about. To conclude the study, the participants were therefore debriefed on the study and disclosed about the Belief in a Just World concept and the hypothesis. Results Using survey condition (accepted vs rejected vs deserved) as the independent variable and whether participants remember what they wrote about as the dependent variable. Furthermore, a manipulation check was proceeded in which we detected a significant, X^2 (4) = 168.63, p .001. Most participants in the accepted condition recalled scripting about accepting someone (83.3%). Participants in the rejected condition recalled scripting about rejecting someone (90.5%). Ultimately, participants in the deserved condition recalled writing about someone got what they deserved. Phi displayed a medium effect. This implies that participants were being attentive to what they were writing about. See Appendix B An One-Way ANOVA was controlled with conditions as the independent variables (Accept v Reject v Deserve) and participants’ agreement rating that the type of person is led toShow MoreRelatedEssay on Quiz Results - Informed Consent1133 Words   |  5 Pagesaction to take for the investigator? Your answer : The investigator can go ahead and enroll the man without a signed consent. Correct Answer : Send a copy of the informed consent via facsimile to the subjects wife. After she has had the opportunity to speak to the investigator, she can sign the informed consent and fax it back. Comment : The IRB will not provide a waiver of consent under these circumstances and the man should not be excluded from the study simply because his legally authorizedRead MoreHealthcare Marketing And Ethical Considerations928 Words   |  4 Pagescare. According to Quinn (2008), the marketing rules that apply to many business settings cannot be applied within the healthcare environment. This is because the average healthcare consumer does not possess adequate medical knowledge to make fully informed decisions. Moreover, a lack of sufficient medical knowledge may cause healthcare consumers to be confused by advertising claims regarding medical advancements or organizational claims to being a cut above the competition (Quinn, 2008). How doesRead MoreRm Citi Modules Essay1283 Words   |  6 Pageswhat received public attention.) Which of the following is included in the Nuremberg Code? Voluntary Consent Informed consent is considered an application of which Belmont principle? **** Respect for Persons (Respect for persons involves respecting individual autonomy in the decision to participate in research. That respect is implemented through the process of informed consent) How should the investigator proceed, with respect to the IRB, after the discovery of the adverse event occurrenceRead MoreA Short Note On A Vulnerable Population For Research Studies1121 Words   |  5 PagesPopulation for Research Elizabeth Smith Evidence Based Practice in Nursing Professor Paula Wellde Abstract Neonates are a vulnerable population for research studies. They are unable to give their own voluntary, informed consent. There are special considerations to obtaining informed consent of neonates with strict guidelines from Health and Human Services, splitting studies into 4 levels and which includes parental permission. The ethical issues surrounding research studies can be navigated usingRead MoreAn Essay Likely About Nothing1334 Words   |  6 Pagesauthority study (Milgram study) 160) IRB continuing review of an approved protocol must: a) Must occur only when the level of risk changes. b) Occur at least annually. c) Must be conducted by a convened IRB. d) Include copies of all signed consent forms. 161) A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator proceed after the discovery of the adverse event occurrence? a) Report the adverse drug experience toRead MoreAngela Carters Family Case Study : The Baby Vs. Mom Case?1305 Words   |  6 Pagessurgery due to the court’s decision. The child lived for two hours, whilst Angela lived for two days. It is said that the surgery contributed as the main reason for her death. The two main dilemmas, in this case, are autonomy and informed consent. Autonomy and informed consent are presented as the two main ethical dilemmas in this case. Munson states that â€Å"The high value we place on autonomy is based on the realization that without it, we can make very little of our lives† (pg. 39). I agree with thisRead MorePhysician Assisted Suicide : A Right Of The People1700 Words   |  7 Pagespain. For those people whose pain does not respond to methods of modern medicine, there should be the option of physician-assisted suicide. â€Å"Physician-assisted suicide refers to the practice of a physician prescribing or regulating, upon a patient’s informed request, a lethal dose of medication for the purpose of ending that patient’s life† (Lerner). The lethal drugs that are given to the patient by the doctor are administered by the patient themself, not by the doctor, so the doctor is not directlyRead More Abortions Pros and Cons Essay1194 Words   |  5 Pages   Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Nowad ays, in this world, there are a lot of problems that can make tremendous conflicts for human beings. They are very complicated and bring a lot of argument and nobody knows what the exact answer is. They also have pros and cons. One of the most complex problems is abortion. This is due to moral and ethical values which we all have. The majority of us are Christians or are brought up in that kind of ambiance which means that as small children we were taught values that are based onRead MoreHuman Experimentation1684 Words   |  7 PagesTOPIC #4: Human Experimentation PRO: Prisoners should be allowed to participate in human research CON: Prisoners should not be allowed to participate in human research History and definitions Dating back to 1965, seventy-five prisoners at Holmesburg prison in Pennsylvania were purposely exposed to a poisonous agent. This study was conducted to determine the effects of dioxin, a potentially harmful substance. Dermatologist Dr. Albert Kligman, exposed prisoners to a dosage 468 times greaterRead MoreSevere Depression1388 Words   |  6 Pagesrelevant trends, pros and cons of medication, steps to take to build a good rapport with your client, know what you are responsible for ethically. We all probably know someone who is severely depressed because, Clinical depression affects millions of people each year (University of Pittsburgh, N.D.). If clinical depression is left untreated it can have serious consequences (it could be life threatening). So it is very important that not only Psychologists are well informed on this topic but