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Dissertations / Theses on the topic 'Consent to medical intervention'

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Published: 4 June 2025
Last updated: 1 August 2025

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1

Heywood, Robert James. "The law and practice of consent to medical intervention." Thesis, Sheffield Hallam University, 2006. http://shura.shu.ac.uk/3197/.

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This thesis explores the challenging concept of informed consent. It is an empirical study investigated in a medico-legal context. The research combines the use of quantitative and qualitative research methods to analyse the different views of the parties who are actively involved in the consent process in both medical and legal settings. The project provides a comprehensive review of the literature concerning the legal aspects of consent and information disclosure, critically analysing relevant case law and academic opinion. The problematic areas are highlighted and from these a number of res
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Scanlan, Camilla Louise. "The Legal and Ethical Limits of Consent in High Risk Medical Interventions: An Empirical Study." Thesis, The University of Sydney, 2015. http://hdl.handle.net/2123/14180.

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That a person’s consent is required prior to any medical intervention, is now well established in law, ethics and medical practice, and is the most profound practical manifestation of respect for autonomy, or self-determination in medicine. For consent to be valid a number of conditions need to be satisfied; the person making the decision must have sufficient capacity (competence) to make the decision; they must have been provided with sufficient information about the proposed intervention and about relevant alternatives such that their decision is adequately informed; the decision must be app
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3

Hutchison, Catherine B. "A randomised controlled trial of an audiovisual patient information intervention in cancer clinical trials." Thesis, University of Stirling, 2008. http://hdl.handle.net/1893/442.

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Introduction and background Recruitment to cancer clinical trials needs to be improved, as does patient understanding about clinical trials, to enable patients to make an informed choice about whether or not to take part. The main reason that clinically eligible patients do not take part in clinical trials is because they refuse; poor understanding of the research has been associated with patient refusal. Audiovisual patient information (AVPI) has been shown to improve knowledge/understanding in various areas of practice but there is limited information about its effect in the cancer clinical
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4

Савченко, О. М. "Правові проблеми згоди пацієнта на медичне втручання". Thesis, Сумський державний університет, 2013. http://essuir.sumdu.edu.ua/handle/123456789/34114.

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Інформована згода на медичне втручання тісно пов’язана з природними правами людини, тобто правом на життя, правом на здоров’я, особисту недоторканність та свободу. Виходячи із сучасних міжнародних стандартів, добровільна згода пацієнта є необхідною умовою правомірності наступного медичного втручання. Проте, законодавчі акти з даної проблеми не в повній мірі забезпечують права і законні інтереси громадян, зокрема, щодо правового регулювання передачі довіреному прав з прийняття важливих медичних рішень у разі втрати довірителем дієздатності. При цитуванні документа, використовуйте посилання http
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5

Baker, Eileen F. "Autonomy and Informed Consent." Bowling Green State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1491391673593916.

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6

Maclean, Alasdair Rhuairidh. "Consent to medical treatment and the competent adult." Thesis, University of Glasgow, 2006. http://theses.gla.ac.uk/5448/.

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In this thesis I analyse the concept of consent to medical treatment. I explore its ethical basis in autonomy and examine how other principles and ethical approaches might interact with the rules derived from autonomy. I then situate the relevant ethical obligations within the context f the healthcare professional-patient relationship which subsequently allows me to develop a textured model of consent. The model is predicated on the theory that consent is a secondary right, derivative on the underlying right which it controls. By giving or withholding consent, the autonomous person determines
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7

Abbey, Erica. "Informed consent as a therapeutic intervention: tailoring expectations to maximize recovery." Thesis, McGill University, 2012. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=110633.

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Informed consent is an integral component of modern medicine; however, gaps between ethical objectives and psychological corollaries linger. Despite mounting evidence to demonstrate its impact on human behavior, physicians and bioethicists scantily construe it as a source of therapeutic influence. Here we explore judicious ways to leverage this standard-of-care tool as both an ethical requisite in the clinical milieu and a procedure, which could either bolster or deflate the health of individuals, perhaps through a placebo effect.First, in a literature review, we examine the history and compo
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8

Crane, Phoenix R. "The POWER of Consent: An Evaluation of Peer-Based Consent Programming in Sexual Assault Prevention." Ohio University Art and Sciences Honors Theses / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ouashonors1493430083169149.

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9

McLean, Sheila Ann Manson. "Information disclosure, consent to medical treatment and the law." Thesis, University of Glasgow, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298800.

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10

Walker, Nancy L. Hamilton. "The relationship between patient perceptions of informed consent and recall of information received during the informed consent process." Virtual Press, 1993. http://liblink.bsu.edu/uhtbin/catkey/865959.

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Informed consent is a requirement by law. Informed consent is a two part process: giving the patient sufficient information so that an educated choice can be made and obtaining assent in writing (Coy, 1989; Fiesta 1991; Sweeney, 1991;). The purpose of this study is to determine the ability to recall information and the perception of patients about the process of receiving information after signing a consent to participate in a large research trial. Patients signing consents for participation in the Breast Cancer Prevention Trial were asked to complete the surveys. Thirty three patients were as
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11

Ibikunle-Salami, Tawa Bimbola. "Educational Intervention to Impact Parental Decisions to Consent to Human Papillomavirus Vaccine." ScholarWorks, 2015. https://scholarworks.waldenu.edu/dissertations/1567.

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Educational Intervention to Impact Parental Decisions to Consent to Human Papillomavirus Vaccine by Tawa B. Ibikunle-Salami MSN, Indiana Wesleyan University, 2010 BSN, Indiana Wesleyan University, 2005 Project Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Nursing Practice Walden University September 2015 Human Papillomavirus (HPV) is a global health issue that is transmitted sexually and affects both genders. Evidence shows that approximately 79 million people are affected in the United States with 14 million newly affected yearly. The Centers for Disease Con
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12

Tronchin, Andrea. "L'intervento medico arbitrario: il problema del consenso." Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3423357.

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Abstract: Thesis title: "The arbitrary medical operation: the problem of consent" This thesis concerns the profiles of criminal implications of medical-surgical treatment performed without the patient's consent. First of all, the referential provisions of the law are identified. For this reason, the foundation of informed consent is analyzed in accordance with constitutional requirements. It is examined closely the gradual change of the doctor-patient relationship. Subsequently, this paper proceeds with the analysis of crimes. In the first place, the question regarding the crime
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13

Hoeyer, Klaus. "Biobanks and informed consent : An anthropological contribution to medical ethics." Doctoral thesis, Umeå universitet, Institutionen för folkhälsa och klinisk medicin, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-358.

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Background: 1985 saw the beginnings of a population-based biobank in Västerbotten County, Sweden. In 1999, a start-up genomics company, UmanGenomics, obtained ‘all commercial rights’ to the biobank. The company introduced an ethics policy, which was well received in prestigious journals, focusing on public oversight and informed consent. Aims: To explore how social anthropology can aid understanding of the challenges posed by the new role of the biobank in Västerbotten, and thus complement more established traditions in the field of medical ethics. An anthropological study of the ethics policy
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14

Hoeyer, Klaus Lindgaard. "Biobanks and informed consent : an anthropological contribution to medical ethics /." Umeå : Univ, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-358.

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15

Devereux, John Anthony. "Competence to consent to medical treatment in England and Australia." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358468.

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16

Barit, Avi. "The doctrine of informed consent in South African medical law." Diss., University of Pretoria, 2017. http://hdl.handle.net/2263/60104.

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17

Morin, Sophie. "La place des droits du patient à l'intérieur de la conception actuelle de l'obligation de renseigner en matière médicale /." Thesis, McGill University, 1999. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=30319.

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This thesis deals with the concept of the medical duty to inform focusing on the rights of the patient. It emerges that the notions governing medical responsibility do not adequately address the question of the protection and application of the rights of the patient. Existing conceptions of the notions of dereliction, causality and damage are analysed in order to point out the many inadequacies with the rights of the patient, source of the obligation to inform. Particular emphasis is given to the situation in Quebec and to the eventual place that could be occupied by conception of the duty to
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18

Fennel, Phil. "Treatment without consent : law, psychiatry and the treatment of mentally disordered people since 1845." Thesis, Cardiff University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297519.

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19

Jerkert, Jesper. "Philosophical Issues in Medical Intervention Research." Licentiate thesis, KTH, Filosofi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163872.

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The thesis consists of an introduction and two papers. In the introduction a brief historical survey of empirical investigations into the effectiveness of medicinal interventions is given. Also, the main ideas of the EBM (evidence-based medicine) movement are presented. Both included papers can be viewed as investigations into the reasonableness of EBM and its hierarchies of evidence. Paper I: Typically, in a clinical trial patients with specified symptoms are given either of two or more predetermined treatments. Health endpoints in these groups are then compared using statistical methods. Con
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20

Cai, Yinghong. "The legal rights in informed consent form for treatment in China." View the Table of Contents & Abstract, 2007. http://sunzi.lib.hku.hk/hkuto/record/B38478730.

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21

O'Regan, Karla Maureen. "Beyond illusion : a juridical genealogy of consent in criminal and medical law." Thesis, London School of Economics and Political Science (University of London), 2014. http://etheses.lse.ac.uk/934/.

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Consent is a concept used frequently and with great significance in a wide array of legal fields. It serves to regulate relationships, legitimize authority, delimit normality, and entrench idealized ways of being in the world. Yet despite the consequence of these functions, there is very little precision within legal scholarship about just what consent is. Few investigations of its definitional content depart from presumptive statements about personal autonomy. These associations are often described as the ‘common sense’ of consent and serve to secure a foundationalist discourse about what con
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22

Lyons, Barry. "'Who is silent gives consent' : power and medical decision-making for children." Thesis, University of Manchester, 2011. https://www.research.manchester.ac.uk/portal/en/theses/who-is-silent-gives-consent-power-and-medical-decisionmaking-for-children(1860645d-78f2-4b89-9524-e32e1b5fa21e).html.

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This thesis seeks to examine how healthcare decisions are made for children, with a particular focus on situations where medical interventions that (1) are not intended to advance the medical welfare of the individual child (eg bone marrow donation and research without therapeutic intent involving young children), or (2) are contrary to the expressed will of the child (e.g. the imposition of life-saving treatment on adolescents who have refused it), are authorised by parents or the state. The authorisation of these procedures is contentious because they breach the child’s bodily integrity whil
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23

Gibb, Winna. "Informed consent : a liberal perspective." Thesis, Queensland University of Technology, 1998.

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24

Lashley, Myrna. "Informed proxy consent : communication between surgeons and surrogates about surgery." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=29068.

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Professionals whose job it is to counsel patients must be cognizant of the role played by communication in the establishment of a trusting working relationship. This is no less true for those within the medical community who must obtain informed consent for surgical interventions than it is for those working within the area of mental health. In order to determine what role communication plays in the obtaining of informed consent within a pediatrics setting, a qualitative study was conducted of 20 surrogates (those individuals giving consent on behalf of legally incompetent children) and of 5 s
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25

Intagliata, Andrew J. "The Relationship of Binge-Drinking and Sexual Consent on Bystander Intervention Attitudes Among College Men." University of Toledo / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1513293528288897.

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26

Bourne, Katie. "Determining capacity to consent in people with learning disabilities." Thesis, n.p, 2000. http://ethos.bl.uk/.

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Pease-Carter, Cheyenne Minton Casey Barrio. "Preferences among student counselors regarding informed consent practices within counselor education." [Denton, Tex.] : University of North Texas, 2008. http://digital.library.unt.edu/permalink/meta-dc-6066.

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28

Plant, Nigel. "The interaction achievement of consent for medical examinations and investigations by healthcare professionals." Thesis, University of Nottingham, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493338.

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Consent has gained an increasing innportance in both health care policy and practice. Research in this subject has focused on information needs of patients (McKeague and Windsor, 2003), and their understanding of information (Turner and Williams 2002). There has been little or no consideration as to how the health professional interactionally seeks the patients consent.
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29

Vaswani, Nileema Ajit. "The role of informed consent in the ethics of medical research on humans." Thesis, University of London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405938.

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30

Lasseter, Gemma Michelle. "Consent study : assessing the public's willingness to provide informed consent for their identifiable general practice medical records to be accessed for different research purposes." Thesis, University of Bristol, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.702735.

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Objectives: Patient involvement in primary care research is often hindered by confidentiality concerns regarding the use of their identifiable medical records. Consequently there is no universal 'pre-consent' process in England, whereby patients provide prior informed consent for their identifiable data to be accessed for different research purposes. This mixed-methods two-phase study investigated patients' opinions about this proposed 'pre-consent' process and the effectiveness of different invitation methods. Methods: Phase 1 used cognitive and semi-structured interview methods to optimise r
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Cai, Yinghong, and 蔡映紅. "The legal rights in informed consent form for treatment in China." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2007. http://hub.hku.hk/bib/B39724347.

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32

Garasic, Mirko Daniel. "Freedom, Consent and Autonomy in Bioethics: justifications for Enforced Medical Treatment and its Refusal." Doctoral thesis, Luiss Guido Carli, 2011. http://hdl.handle.net/11385/200898.

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On Autonomy. Anorexia Nervosa: enforcing medical treatment to keep a person alive. The Singleton case: enforcing medical treatment to put a person to death. The inconsistent use of Autonomy: additional cases and doubts. A more consistent notion of Autonomy in relation to refusal of treatment.
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Torres, Roberto. "Communicating informed consent with LEP participants during clinical trials| A case study." Thesis, University of Phoenix, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3691421.

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<p> Healthcare systems are under pressure to eliminate disparities of care. Communication methods used with Limited English Proficiency (LEP) patients was presented in the literature as an essential component to deliver quality and equal care. Several strategies have been implemented to assess and target the communication methods between patients and health care teams. The challenge for health systems workers is to address communication barriers to eliminate disparities of care and medical errors. The purpose of the present qualitative case study was to explore if communication barriers affect
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34

Anthony, John. "The justfiable limitations of patient autonomy in contemporary South African medical practice." Thesis, Stellenbosch : University of Stellenbosch, 2009. http://hdl.handle.net/10019.1/2859.

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Thesis (MPhil (Philosophy))--University of Stellenbosch, 2009.<br>ABSTRACT: The European Enlightenment secured man’s freedom from doctrinal thought. Scientific progress and technological innovation flourished in the 18th Century, radically changing the lives of all. Man’s mastery and transformation of his environment was matched by revolutionary political reform, resulting in the dissolution of empire and the transfer of power into the hands of the people. Social transformation saw the city-states of pre-modern man supplanted by a globalized community whose existence grew from time and
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Kerner, David Neal. "Impact of a decision aid videotape on young women's attitudes and knowledge about hormone replacement therapy /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1998. http://wwwlib.umi.com/cr/ucsd/fullcit?p9901432.

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36

Rollnick, Stephen. "Brief intervention for excessive drinkers in a medical setting." Thesis, Cardiff University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367933.

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37

Nan, Yucen. "High-Credibility Edge Analytic System for Early Medical Intervention." Thesis, The University of Sydney, 2022. https://hdl.handle.net/2123/27309.

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The tremendous upsurge in the size of datasets has started gaining momentum a decade ago in science, finance, and every slice of our everyday life. The same scenario of the data volume explosion also arose in medical healthcare, and the elaborate management and exhaustive exploration of these heterogeneous data play important roles in modern medical care services. Traditional healthcare systems have been unable to cope with this complicated situation. After the popularity of digitized medical records and the evolution of the worldwide network interconnection, cloud computing has been proposed
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38

Flanagan, Ellen Cecelia. "AN URBAN BIOETHICS APPROACH TO PARENTAL INFORMED CONSENT FOR PEDIATRIC CLINICAL RESEARCH." Master's thesis, Temple University Libraries, 2018. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/537038.

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Urban Bioethics<br>M.A.<br>In the current healthcare landscape, parents generally make decisions regarding whether or not their children are allowed to take part in clinical research, with the general assumption being that parents know what is best for children. Investigations have been conducted regarding what is likely to lead parents to consent or not consent to their child’s participation in a trial, but research plans seldom incorporate the consideration that not all parents come into the consent process with equal social, academic, and economic footing. Since the burden of the ultimate d
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Pease-Carter, Cheyenne. "Preferences among student counselors regarding informed consent practices within counselor education." Thesis, University of North Texas, 2008. https://digital.library.unt.edu/ark:/67531/metadc6066/.

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The purpose of this study was to investigate student preferences for content, timing, and method of informed consent within counselor education programs. Participants included 115 students enrolled in counseling internship courses at six counseling programs accredited by the Council for Accreditation of Counseling and Related Educational Programs (CACREP). Participants completed the Informed Consent Preferences Questionnaire (ICPQ), an instrument designed specifically for this study through systematic instrumentation development. Descriptive statistics highlighted participants' moderate to hi
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Kious, Brent Michael. "The evidentiary account of consent's moral significance." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=1930280011&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Hjelmström, Anna. "Primary Hyperparathyroidism– the Choice of Intervention." Thesis, Örebro universitet, Institutionen för medicinska vetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-66797.

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42

Milliano, Paul Augustinus René de. "Influence of medical intervention on sympathetic activity in heart failure." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2002. http://dare.uva.nl/document/85802.

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Elhawary, Haytham. "MRI compatible mechatronic devices to aid medical diagnosis and intervention." Thesis, Imperial College London, 2008. http://hdl.handle.net/10044/1/11321.

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The excellent soft tissue contrast of Magnetic Resonance Imaging (MRI) makes it an invaluable tool for guiding and monitoring interventional procedures. This has encouraged the development of MR compatible manipulators capable of combining the high precision and repeatability of robotic systems with the image capabilities of MRI. A system capable of performing transrectal prostate biopsy inside a high field 1.5T MRI scanner was developed to improve the pathological diagnosis of prostate cancer. The 5 DOF device is actuated using piezoceramic motors and can position an endorectal probe inside o
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Tamin, Jacques. "The doctor-patient relationship, confidentiality and consent in occupational medicine : ethics and ethical guidance." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/the-doctorpatient-relationship-confidentiality-and-consent-in-occupational-medicine-ethics-and-ethical-guidance(586107a4-ffe5-40be-ad19-acb9d329d732).html.

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This thesis seeks to examine the ethical basis for occupational medicine, as it is practised in the United Kingdom (UK). There is empirical evidence of occupational physicians being confused with regard to confidentiality and consent, and variations in their practice. It is argued that the ethical guidance from the General Medical Council and the Faculty of Occupational Medicine on these matters, contributes significantly to such confusion. The doctor-patient relationship, consent for disclosure of a medical report, and medical confidentiality, all in the context of occupational medicine pract
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Kettle, Nancy M. "Informed consent: its origins, purpose, problems, and limits [electronic resource] / by Nancy M. Kettle." University of South Florida, 2002. http://purl.fcla.edu/fcla/etd/SFE0000041.

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Title from PDF of title page.<br>Document formatted into pages; contains 165 pages.<br>Thesis (M.A.)--University of South Florida, 2002.<br>Includes bibliographical references.<br>Text (Electronic thesis) in PDF format.<br>ABSTRACT: The doctrine of informed consent, defined as respect for autonomy, is the tool used to govern the relationship between physicians and patients. Its framework relies on rights and duties that mark these relationships. The main purpose of informed consent is to promote human rights and dignity. Some researchers claim that informed consent has successfully replaced pa
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Tomita, Kiyomi. "Informed consent and the right to refuse medical treatment : a comparative study of common-law Canada and Japan." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=61156.

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Common law in Canada recognizes the rights to self-determination and autonomy and the right of competent persons to decide for themselves on medical treatment which includes the right to refuse all treatment. The legal profession has caused Japanese law to begin to recognize these basic rights, however professional and societal factors combine to accord the Japanese physician a wide discretion to determine what information to disclose, especially in the case of cancer. This thesis examines the similarities and differences existing between Canada and Japan in the controversial area of informed
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47

Lieblich, Eliav. "Intervention in Civil Wars: Intervention and Consent." Thesis, 2012. https://doi.org/10.7916/D86H4QJF.

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In modern international law, it is a near consensus that no state can use force against another - the main exceptions being self-defense and actions mandated by a U.N. Security Council resolution. However, one more potential exception exists: forcible intervention undertaken upon the invitation or consent of a government, seeking assistance in confronting armed opposition groups within its territory. This dissertation seeks to analyze the consent-exception in a wide context, and attempting to delineate its limits - including, perhaps, cases in which government consent power is not only negate
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48

Podolská, Marie. "Zásah do integrity člověka." Master's thesis, 2018. http://www.nusl.cz/ntk/nusl-373192.

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Physical and mental integrity of an individual represents one of the components of a human personality, which may be regarded as a personal sphere of everyone and which is protected by the law against any unauthorized interference. Legislation regarding the interference with the integrity of an individual is based on the principle of inviolability of a human being, according to which no one is entitled to interfere with the integrity of another individual without his consent, except as provided by law. The consent of the individual concerned is therefore the most fundamental circumstance exclu
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JHU, YU-CHEN, and 朱育辰. "The Inapplicability of Informed Consent to Medical Criminal Law - The Position of Patients’ Consent in Medical Criminal Law." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/azwej4.

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碩士<br>國立臺北大學<br>法律學系一般生組<br>106<br>The development of informed consent is to guarantee the right of patients’ self-determination. It is generally accepted by the general public that doctors should obtain patients’ consent by informing the medical treatment. And doctors’ explanation of medical behaviors to patients is also called doctors’ duty of disclosure. With the bad communication between doctors and patients is lead to the increasing of the medical lawsuits. Especially, doctors will be subject to criminal accusation by violating the doctrine of informed consent. However, whether doctors
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Wu, You-Lin, and 吳侑臨. "A study on the Medical Informed Consent." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/vh42ru.

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碩士<br>亞洲大學<br>財經法律學系<br>107<br>“Informed Consent”—doctor’s duty to inform—is the premise of the right of patient autonomy. Without emphasizing the importance of the duty, one cannot make a concrete discourse on the right. When the right has been the center of legal-medical discussion/debate for years, the duty has been transformed from a medical ethic issue into a legal obligation in Taiwan. Regardless of the aforementioned transformation, a thorough legal examination and discussion has not yet been made in Taiwan. This thesis intends to fill the research blank, and discuss the duty, start
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