Ethical Considerations: The Meaning And Implications Of Informed Consent

Decent Essays
Ethical Considerations
The participants will be informed of the nature of research and requested to sign the informed consent form prior to them completing the questionnaires. The meaning and implication of informed consent will also be verbally explained to the participants prior to their completing the questionnaires. Research participants shall be informed that they will be free to withdraw from the research at any stage if they will feel that they no longer want to participate. The data collected will be treated with utmost confidentiality during and after the research and used only for the intended research purpose.

Related Documents

  • Decent Essays

    The SOA 2003 now also recognizes the concept of informed consent. Informed consent is an agreement which a person makes after getting to know all the relevant facts. This means a person will only consent when all the facts are become known. For example, a patient consenting to a medical procedure. Informed consent is demonstrated in the case of Dica.…

    • 195 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Tuskegee Violations

    • 1279 Words
    • 6 Pages

    While conducting a study, it is required of a researcher to do no harm, receive informed consent, ensure voluntary participation, and to not take advantage of, or wrongly include, protected and vulnerable populations. To do no harm entails that any person who joins a study will not be exposed to any more harm than they would on a regular basis. Informed consent requires that a subject is aware they are part of a study while also fully understanding the aspects the study will involve. Voluntary participation is a partakers right to decide whether or not they want to be a part of a study while aware of the option to back out at any time without repercussion. Finally, with protected and vulnerable populations, a researcher has the responsibility of providing special methods or requirements for groups like prisoners, children, and the educationally disadvantaged.…

    • 1279 Words
    • 6 Pages
    Improved Essays
  • Superior Essays

    Legally, our society has become more litigious as a valid consent is beneficial to protect both parties. A person could accuse a healthcare professional or researcher of trespass and assault if the person did not give their consent or if it was not voluntarily. If an individual is not sufficiently informed of the consequences of their decision and they suffer as a result, they can accuse the healthcare professional or researcher of negligence. This is the claim that had been introduced in the Canterbury v. Spence Court case, which argued for a reasonable patient standard with respect to informed consent from a patient’s physician. The procedural legality of the American justice system has indeed led Katz to raise concerns over the very implications…

    • 973 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    Informed consent is essential in nursing practice as it allows patients and health care providers to communicate effectively. It is not just signing a document instead it is used to inform the patient of, risk, alternative, benefit, and understanding of a procedure or treatment. Informed consent gives the patient the right to received treatment and the right to refused treatment or any other intermediations. However, there are three elements that the Joint Commission necessitates that health care providers must consider before offering the patient an informed consent including the information, voluntary consent, and competence (Westrick, 2014).…

    • 463 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Informed Consent and Participants- letting the participants know, understand, and comprehend the information from the research and the ability to consent or decline study voluntarily. Informed consent can be written (7th or 8th grade level) and orally presented witnessed by a third party. “Implied consent” is when a returned questionnaire shows voluntary consent for participation. Participant’s sign consent to access their health information Confidentiality Procedure- participants data need to be kept confidential through anonymity, the use of identification number, applying for a Certificate of Confidentiality, debriefing session, open communication, and referrals to other…

    • 864 Words
    • 4 Pages
    Improved Essays
  • Great Essays

    The HeLa incident at John Hopkins Medical Institute in the 1950’s highlighted the importance of informed consent in the medical field, it provides a strong example for the ethical and legal repercussions for disobeying the process and violating a patient’s unalienable human rights, and furthermore reinforces its need. Informed consent is the undeniable prerequisite for a patient to be fully informed of a procedure and all of its aspects. This process is a necessary and pragmatic approach to maintaining a positive relationship between a physician and their patient; a necessity in ensuring human autonomy and the preservation of human rights. Informed consent was originally devised by the United Nations Committee in the Nuremberg Code to prevent future atrocities such as the Holocaust and Nazi experimentation on the Jews. The code is a set of ethics principles for researchers and physicians, it is aimed at ensuring that doctors do not take advantage of patients.…

    • 1431 Words
    • 6 Pages
    Great Essays
  • Improved Essays

    Informed consent is based on legal and ethical issues in relation to a person’s healthcare. The consumer must be given information on their illness, treatments or any procedures that are to be done in a way that in understandable to them. If English is not their first language, or there is a language barrier of any type, then a translator should be provided. With this information, they should be able to make an informed decision about their care. This falls under a consumer or patient’s autonomy, or the right to govern and make decisions for themselves.…

    • 461 Words
    • 2 Pages
    Improved Essays
  • Decent Essays

    Informed consent is the right a patient has to determine what is done to their body. The person must be well informed as well as volunteer for informed consent to work. Today, many people talk about how one is to decide if a person is competent or not and who is to make that ultimate decision if someone really is competent or not. My question is do you think the age limit should be reevaluated on informed consent? Eighteen seems to be such a standard age on our country for things to become legal, but if there is a fifteen year old child who has battled cancer for three years, shouldn't they be able to decide things for themselves, assuming they have sufficient knowledge of their diagnosis at this point?…

    • 233 Words
    • 1 Pages
    Decent Essays
  • Decent Essays

    Informed Consent

    • 431 Words
    • 2 Pages

    1. All subjects will have two meetings regarding the informed consent form. The first will be a group session before the medical testing and will discuss the study purpose, goals, design, and what their participation entails. Furthermore, study design will be explained thoroughly such as what placebo-controlled means and what a sentinel block is. The second meeting will be a one-on-one session with subjects after completing their medical tests.…

    • 431 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Medical treatment helped millions of people, but there are responsibilities that all health care professionals must abide by to ensure patients’ rights are supported. The established presumption is that every adult of sound mind has the right to decide what will be done to his or her body. Before any treatment is carried out on the patients’ body by any HCP, their consent must be obtained. Consent to treatment can be verbal, written or gestured/implied. The patient must have the capacity or competence, consent is given voluntarily and covers the procedure in question and the patient was informed clearly of the treatment and their risks.…

    • 583 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Informed Consent Process

    • 1673 Words
    • 7 Pages

    Presentation of the problem: Client is unaware of career interest and is interested in obtaining a college major. Within the first week of working with Leslie, the implementation of informed consent will take place. Also, the Strong Interest Inventory (SII) and Myers-Briggs Type Indicator (MBTI) will be provided via computer to obtain a comprehensive career report. The comprehensive report will guide the career counselor and Leslie toward the specific outcomes and goals relating to her career interest. Leslie and her mother will be present during the informed consent process.…

    • 1673 Words
    • 7 Pages
    Improved Essays
  • Superior Essays

    Evidence Based Practice

    • 873 Words
    • 4 Pages

    For research and education, none of the study mentioned the informed consent and protection of the subject responding to the questionnaire or according the…

    • 873 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    Informed Consent

    • 672 Words
    • 3 Pages

    Page 421 Consent is the voluntary agreement by a person who possesses sufficient mental capacity to make an intelligent choice to allow something proposed by another to be performed on themselfs (Pozgar, 2013, pg. 404) . Consent must be obtained prior to any medical procedure (Pozgar, 2013, pg. 404). Express consent can take the form of either verbal agreement or can be accomplished through the execution of a written document authorizing care (Pozgar, 2013, pg. 404). Implied consent is determined by the act of silence (Pozgar, 2013, pg. 404) The two forms to express consent can be either verbal or written documentation (Pozgar, 2013, pg. 404).…

    • 672 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    One can conclude, that there are not very many risks to receiving services. These programs increase the participants’ self-esteem and quality of life. In other words, these programs have a positive psychological influence on these individuals. As such, risks to receiving services could be considered to be very minimal. However, participants could encounter risks to receiving services in the healthy relationships program.…

    • 576 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    wants to conduct a study using people, they must get permission from the participants. Obtaining this permission is important because it ensures that participants will be informed regarding the purpose of the project, the procedures, the duration, the risks and benefits, the commitment to confidentiality, the use of the findings and results, and how to resign from the study if desired. Informed consent is critical to the efficacy of the study because it gives the researcher an opportunity to ask other clarifying questions that might affect the results. Researchers need to ensure that participants’ psychological reasonableness has not been impaired by severe mental illness, drinking or drugs, emotional distress, and other factors that might skew final results. Informed consent is a significant ethical principle that gives credibility to the study and the researcher.…

    • 1468 Words
    • 6 Pages
    Improved Essays