This website uses cookies to ensure you have the best experience. Learn more

Informed Consent Summery Report

569 words - 3 pages

Informed Consent Summary Report
students???
BSHS/ 322- Professional, Ethical, and Legal Issues in Human Services
Prof. Theresa Edwards

The four elements of informed consent are competence, voluntariness, full information, and comprehension. In order to fully understand your rights you must possess the following criteria’s. If a person is not informed, they are unable to make a justified decision regarding their situation and therefore, can be misled and potentially make a determination that is not fully based on facts.
The Kids in Crisis Agency takes confidentiality very serious and is a vital part of the intake process for the residents and individuals who are to become employed here. Informed consent documents here imply that all information that is provided to the agency will remain confidential aside from certain specific ...view middle of the document...

This is explained during any intake procedure and also explained to the individual at the moment they make any statements.
The Authorization of Disclosure form for Kids in Crisis is very straight to the point and easy to comprehend. It gives a start and end date, states that the client has the right to revoke disclosure at any time and describes why the disclosure is needed. In the Mass Immunization Clinic Encounter Form the disclosure is very informative and clear to make sure that the patient is fully aware of the risks and benefits of receiving immunizations. It discloses who will be handling the forms and for how long they will be kept on file. It also includes the Code of Virginia for additional testing for HIV, Hepatitis B or C in the event the blood of the patient comes in contact with anything that is contaminated. The final form, Infant & Toddler Connection of Virginia Notice and Consent to Determine Eligibility, the agency is requesting consent to assess the child to make sure they meet certain eligibility requirements. The form is very wordy but carefully describes reason for notice, action proposed, description and timelines so that the parent is aware of why the assessments are being conducted. The form also provides a section describing what consent means so that the parent is aware of their rights to grant consent and to ensure that the parent understands and agrees to the terms before signing the form.
All of the informed consent documents critiqued met the four criteria of the Informed Consent section in the text. Although the forms had different ways of presenting the information, all were very clear on what the consent requested was needed for in order for the client to make a well informed decision on whether or not to agree to the terms.

References
Prince William County Government Agency- Department of Health
http://www.pwcgov.org/government/dept/health/Documents/CHS%202b%20Informed%20Consent.pdf

Other Papers Like Informed Consent Summery Report

Law Case Study

2098 words - 9 pages abortions, how much should be the state involved, what are the moral and ethical views regarding this issue. This controversy divided nation into pro-choice and pro-life debate. Many states openly resisted the Roe v. wade and passed new law that prohibited abortions. Pennsylvania created procedural hurdles for women seeking abortions. Pennsylvania Abortion Control Act requires a woman seeking an abortion must give informed consent. She must be

Reporting

3631 words - 15 pages report contains many illustrations, the list of illustration is given immediately after the table of contents. This list gives the number, title and page reference of each illustration. Exicutive Summary: A synopsis is a brief overview of report’s most important. It is also called abstract. Executive summery is a fully developed mini version of the report and is comprehensive. B) Report Body: The body is the posses of a report. Here the

Term Paper

1069 words - 5 pages proposed amendments involve modifications to: | |1) Informed Consent / Assent Forms No Yes*(if yes, re-Consent of previously enrolled subjects? | |No Yes, if yes, please explain process in section D and provide copy of amended Informed Consent Form

Critical Appraisal of a Research Report

1317 words - 6 pages Considerations Ethical considerations associated with this research study included consent of participation, safety of the participants and privacy of participants’ information. Investigators met the required standards of clinical research by obtaining consent of participation prior to the study. According to the World Health Organisation, research investigators are required to obtain informed consent from research participants by issuing them with

Ethical Healthcare Issues Paper

1427 words - 6 pages think (Morrison, 2011). Healthcare providers need to respect patients who may not want any treatment that go against morals and values. Legal and ethical framework considering the development guidelines for transfusion of blood in adults and children apply to ethical principles should have informed consent (Grainger, 1997). It is unethical to precede any blood transfusions without consent, information, and respecting patient’s rights. Physicians

Ethical Research

1082 words - 5 pages is now required reading for everyone involved in human subject research. The ETHICAL RESEARCH 3 Belmont Report identifies three basic ethical principles regarding all human subject research: respect for persons, beneficence, and justice. Respect for persons requires medical researchers to obtain informed consent from their study

Milgrams Background

1569 words - 7 pages ) study there were many ethical concerns which arose with his study on obedience to authority, the study had left participants who took part in the experiment with not physical but mental distress (Benjamin & Simpson, 2009). There were many discussions in relation to ethical questions which were raised. The key area of ethical guidelines known as deception, debriefing, confidentiality and informed consent are the key areas in Milgram’s (1963) study

Obstetric Consent for the Use of Epidural Anesthesia

1720 words - 7 pages emotional support are nursing responsibilities. She should also be informed that a Foley catheter will be necessary post procedure as she will lose the ability to control GU function. Consent for the Foley insertion is separate and should be obtained along with the epidural consent. Once she understands the procedure in its entirety she can sign the consent form in the presence of a nurse. Implementation The nurse will remain at

Hsc Unit 503

1959 words - 8 pages reasonable individual using relevant information about the advantages and disadvantages of ll the possible courses of action, in accord with the individual’s beliefs For an individual’s consent to be valid, it must be voluntary and informed, and the person consenting must have the capacity to make decisions. Voluntary- the decision to consent to treatment must be made alone, and must not be due to pressure by staff, friends or family

Hope and the Limits of Research

680 words - 3 pages headache, weakness etc. From this point, I think, a third party observer rather than Dr.Tetler should be involved for a independent observation. Clinical trial is the corner stone of advancement of medical science. Clinical trial data obtained from human subjects will eventually benefit population at-large. However, ethical considerations before, during and after clinical trial as well as a fully informed consent are equally important as the scientific portion of a clinical trial.

Legislative Framework - Vulnerable Adults

2191 words - 9 pages , relationship or situation which constitutes the alleged or suspected abuse? ➢ Does the person now give meaningful consent to any preventable action, investigation or report. It is also necessary to determine both whether the person could consent and whether they did consent. Abuse may occur when any of the following conditions apply; ▪ The person does not consent; ▪ The person is unable to consent, either because of issues of capacity

Related Essays

Respect For Persons,Beneficence, And Justice Essay

1756 words - 8 pages areas of his life the issue that is relevant to the case was whether he possessed the capacity to make an informed consent. Informed Consent The nine basic rules4 for an informed consent are 1. Identifying the appropriate decision maker 2. Having the discussion at a time when the patient is not distracted or in great pain. 3. Determine that the patient is communicating voluntarily 4. Disclose a

Biomedical Essay

1501 words - 7 pages . 1. A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator proceed, with respect to the IRB, after the discovery of the adverse event occurrence? Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. 2. How long is an investigator required to keep consent

Week 2 Homework Excerse Essay

1231 words - 5 pages therefore, needs to be proved or disproved through research and data analysis. 4. Describe the content that should appear in a well-written informed consent form for a research study. Why is it important to obtain informed consent? What are the three principles outlined by the Belmont Report? What additional concerns do you have (if any) when obtaining consent from a minor? Because informed consents can at time be technical and in some ways

Irb Proposal Essay

741 words - 3 pages : __________________________________ Note: Before applying for human subjects review, the Masters Project or Thesis proposal must be formally approved by the project or thesis committee, and a copy of the informed consent must accompany this form to the Institutional Review Board (IRB). I hereby certify that upon approval of this proposal by the IRB, no changes will be made without approval of the IRB, and that any problems, adverse reaction