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Ethics in psychology ethics
Ethics in psychology ethics
Critics on milgram experiment on obedience
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The British Psychological Society’s Ethical Principles for Conducting Research with Human Participants code was revised and published in 1990. This code was a universally used document; many institutions and research funding bodies have used the code to inform their own research ethic policies and practices. The understanding of ethics in research are continuously changing and evolving which has led to the revisions of the British Psychological Society’s Code of Ethics and Conduct being revised in 2006 and 2009, these revisions have also influenced thinking in this area. There are diverse reasons as to why it is important for research to be ethical. It is becoming increasingly important that participants should have confidence in their investigators …show more content…
Participants need to know what it is they are agreeing to, although some studies require deception which is acceptable if the participant is fully debriefed after their participation in the study. The participants need to know and be constantly reminded that they have the right to withdraw at any time before, during or after the experiment. The participant has the right to ask for their data to be fully or partially destroyed and therefore their data will not be used in any part of the research. It is important to explore who is able to give informed consent; participants under the age of 18 would need to get consent on their behalf from either a parent or guardian. Also those who are mentally or physically impaired which may result in them being unable to provide informed consent, similarly to children, may need to get a guardian or parent to give consent on their behalf. The term ‘informed’ means that the consent forms should be accompanied with an information sheet which includes details of what the participant should expect from the experiment, details of the investigators and how they can be contacted. It is acceptable to not receive informed consent as long as what happens to the participants could occur in their everyday …show more content…
Type 1; deliberate misleading of participants which may include the use of confederates, staged manipulations in field experiments such as deceptive institutions. Type 2; deception by omission which could be creating ambiguity and failure to enclose fill information about the study prior to the study commencing. Researchers should avoid deceiving participants about the nature of the research unless there is no alternative; this would require to be deemed acceptable by an individual expert. Milgram (1963) was highly criticised for his obedience study. Participants were recruited as volunteers for a lab experiment which was investigating ‘learning’. Participants were made up of 40 males, aged between 20 and 50, whose jobs ranged from unskilled to professional, from the New Haven area. Although they volunteered to participate in the study, they were paid $4.50 for just turning up. Each participant was introduced to another participant, who was actually a confederate. They picked straws to determine their roles, either a learner or teacher; this was fixed and the confederate was always the learner. The learner was strapped to a chair with electrodes, in a separate room to the participant who was
Those who were affected by the testing in hospitals, prisons, and mental health institutions were the patients/inmates as well as their families, Henrietta Lacks, the doctors performing the research and procedures, the actual institutions in which research was being held, and the human/health sciences field as a whole. Many ethical principles can be applied to these dilemmas: Reliance on Scientific Knowledge (1.01), Boundaries of Competence (1.02), Integrity (1.04), Professional and Scientific Relationships (1.05), Exploitative Relationships (1.07, a), Responsibility (2.02), Rights and Prerogatives of Clients (2.05), Maintaining Confidentiality (2.06), Maintaining Records (2.07), Disclosures (2.08), Treatment/Intervention Efficacy (2.09), Involving Clients in Planning and Consent (4.02), Promoting an Ethical Culture (7.01), Ethical Violations by Others and Risk of Harm (7.02), Avoiding False or Deceptive Statements (8.01), Conforming with Laws and Regulations (9.01), Characteristics of Responsible Research (9.02), Informed Consent (9.03), and Using Confidential Information for Didactic or Instructive Purposes (9.04), and Debriefing (9.05). These particular dilemmas were not really handled until much later when laws were passed that regulated the way human subjects could be used for research. Patients
The IRB is an administrative body which has been established to make sure research participants' rights are protected. IRBs review all aspects of the researchers' project: the study design, the recruitment process, the participant population, the informed consent document and process, the risk/benefit ratio, privacy and confidentiality, data storage and protection, and safeguards for vulnerable participants (University of St. Francis, n.d.). In this way, participants' rights are protected because the effort is made even before the research begins. The review process ensures that participants are chosen fairly and informed adequately and the information collected during research is safeguarded through collection, use, and storage. Research using human participants is such an important part of medicine that it is imperative it is performed in a way that its intrigue is not compromised.
Those participating were also led to believe that their contribution went to a worthy cause – to advance knowledge and understanding of learning processes. They were also told that the victim (the learner), was taking part voluntarily meaning they had an obligation to fulfill even if it became unpleasant (also applies to the teacher). Additionally, the volunteers were being paid, which created a further sense of commitment to the investigation. Those who took part also had little knowledge about how psychological experiments ran, as Milgram’s study was most likely the first one they ever partook in. Therefore, they had little knowledge about the rights and expectations of the situation, and felt more confined than if they had been through a similar experience prior.
Where possible, participants are asked for their consent to be part of the study, if under 18 then parental consent will be needed. If it is impossible to ask the participants for consent, then a similar group of people will be asked if they would be ok in participating in the experiment. All participants must be given information regarding the purpose of the study, foreseeable risks, length of time the subject is expected to participate as well as other things.
In qualitative studies, the researchers are unaware of the interview is likely to untwist. Therefore, informed consent is a must.
In social psychology, these psychologists have an obligation to use their research skills to advance our knowledge of human behaviour, for the ultimate aim of human betterment. Milgram’s study into obedience involved participants becoming a ‘teacher’ and applying an electric shock to the ‘learner’ (who was a confederate) when they answered a word association question incorrectly. The participant was not aware that the shocks they administered were false and some believed they may have killed a man. In this instance therefore, the code of conduct and ethical guidelines published by the British Psychological Society (BPS) and American Psychological Society (APS) in 1993 were broken in more than one way.
Informed consent is the basis for all legal and moral aspects of a patient’s autonomy. Implied consent is when you and your physician interact in which the consent is assumed, such as in a physical exam by your doctor. Written consent is a more extensive form in which it mostly applies when there is testing or experiments involved over a period of time. The long process is making sure the patient properly understands the risk and benefits that could possible happen during and after the treatment. As a physician, he must respect the patient’s autonomy. For a patient to be an autonomous agent, he must have legitimate moral values. The patient has all the rights to his medical health and conditions that arise. When considering informed consent, the patient must be aware and should be able to give a voluntary consent for the treatment and testing without being coerced, even if coercion is very little. Being coerced into giving consent is not voluntary because others people’s opinions account for part of his decision. Prisoners and the poor population are two areas where coercion is found the most when giving consent. Terminally ill patients also give consent in hope of recovering from their illness. Although the possibilities are slim of having a successful recovery, they proceed with the research with the expectation of having a positive outcome. As stated by Raab, “informed consent process flows naturally from the ‘partnership’ between physician and patient” (Raab). Despite the fact that informed consent is supposed to educate the patients, it is now more of an avoidance of liability for physicians (Raab). Although the physician provides adequate information to his patient, how can he ensure that his patient properly ...
Truog, Robert D., Walter Robinson, Adrienne Randolph, and Alan Morris. "Is Informed Consent Always Necessary For Randomized, Controlled Trials?" The New England Journal of Medicine 340, (March 1999): 804-807.
To begin, to those who may wonder what informed consent is, it is a legal and ethical prerequisite for clinical research on humans (Bristol, par 2). The purpose of informed consent is to ensure that patient autonomy is respected in decisions about their healthcare (Susilo, 1). Many people say that the term was first used in 1957. There was a malpractice case with Salgo v Leland Stanford Jr. The California Supreme court stated that no patient can submit to a medical intervention without having given “informed consent”. Even though the courts had said this, inf...
The purpose of this essay is to introduce the concept of consent, briefly identify its types and legal fundaments, examine significance of consent in a healthcare provision and illustrate the main issues involved with patients’ consent with midwifery practice as the focal point of interest.
Ethics refers to the values and customs of a community at a particular point in time. At present, the term ethics is guided by the moral principles that guide our everyday actions. These moral principles guide the researcher into deciding what is ‘right’ or ‘wrong’. The foundation of medical ethics is governed by two philosophical frameworks that are deontology, and utilitarianism. However ultimately the ethics committees need to balance the risks, and benefits for the participants and the community associated with the particular research proposal. This balance is quite important as the well being of participants is at risk.7
Before the study begins the researcher must outline to the participants what the research is about, and then ask their consent to take part (McLeod, 2007). Alex was only granted an opportunity to reduce his prison sentence by participating in an experiment. However, he was completely unaware of what the procedures consisted of and only realized each event as he went along with the process. Participants must be given information relating to procedures involved in the research, benefits of the research, and all foreseeable risks and discomforts to the individual (McLeod, 2007). The only information that Alex was given was that the experiment was going to make him better, shorten his sentence, and involve him watching films.
In conclusion, obtaining informed consent is a vital part of respect for the patient and safeguarding of self-determination. The consent to participate in research or treatment should be informed, comprehensible, and free of coercion. There is not a clear black and white answer because no matter what is done to assure informed consent there is always a moment of doubt on the end of the patient as to whether what is going to take place is fully understood and their true wishes honored.
America Psychological Association. (2010). Ethical Principles of Psychologists and Code of Conduct. Retrieved 02 09, 2011, from America Psiychological Association: http://www.apa.org/ethics/code/index.aspx
This experiment consisted of 40 males between the age of 20-50. Milgram followed through with this experiment to recognize the relationship between authority and obedience. Milgram selected confederates that knew about the experiment to be the