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Artykuły w czasopismach na temat "Informed consent"
Lie, Rico, i Loes Witteveen. "Visual informed consent: informed consent without forms". International Journal of Social Research Methodology 20, nr 1 (11.12.2015): 63–75. http://dx.doi.org/10.1080/13645579.2015.1116835.
Pełny tekst źródłaYU, Ho-Jong. "Doctors Duty of Informed Consent and Patient Informed Consent Form". Korean Journal of Medical Ethics 5, nr 1 (czerwiec 2002): 27–41. http://dx.doi.org/10.35301/ksme.2002.5.1.27.
Pełny tekst źródłaMoody, Harry R. "From Informed Consent to Negotiated Consent1". Gerontologist 28, Suppl (1.06.1988): 64–70. http://dx.doi.org/10.1093/geront/28.suppl.64.
Pełny tekst źródłaLiew, J., i M. Winston. "Informed consent". British Dental Journal 230, nr 2 (styczeń 2021): 59. http://dx.doi.org/10.1038/s41415-021-2614-y.
Pełny tekst źródłaMyers, William R. "Informed Consent". Oral and Maxillofacial Surgery Clinics of North America 5, nr 1 (luty 1993): 179–84. http://dx.doi.org/10.1016/s1042-3699(20)30678-6.
Pełny tekst źródłaTait, Ann. "Informed consent". Nursing Standard 3, nr 36 (3.06.1989): 51. http://dx.doi.org/10.7748/ns.3.36.51.s74.
Pełny tekst źródła&NA;. "Informed consent". Inpharma Weekly &NA;, nr 1201 (sierpień 1999): 20. http://dx.doi.org/10.2165/00128413-199912010-00043.
Pełny tekst źródłaWilson, Peter, i P. Gerber. "Informed consent". Medical Journal of Australia 142, nr 13 (czerwiec 1985): 704–5. http://dx.doi.org/10.5694/j.1326-5377.1985.tb113604.x.
Pełny tekst źródłaDrew, J. H. "Informed consent". Medical Journal of Australia 143, nr 3 (sierpień 1985): 129. http://dx.doi.org/10.5694/j.1326-5377.1985.tb122855.x.
Pełny tekst źródłaCotton, Peter B. "Informed consent". Gastrointestinal Endoscopy 96, nr 1 (lipiec 2022): 163. http://dx.doi.org/10.1016/j.gie.2022.03.018.
Pełny tekst źródłaRozprawy doktorskie na temat "Informed consent"
Baker, Eileen F. "Autonomy and Informed Consent". Bowling Green State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1491391673593916.
Pełny tekst źródłaGibb, Winna. "Informed consent : a liberal perspective". Thesis, Queensland University of Technology, 1998.
Znajdź pełny tekst źródłaAveyard, H. "Does informed consent theory inform nursing practice? : an exploration of the application of informed consent prior to nursing care procedures". Thesis, King's College London (University of London), 2000. https://kclpure.kcl.ac.uk/portal/en/theses/does-informed-consent-theory-inform-nursing-practice--an-exploration-of-the-application-of-informed-consent-prior-to-nursing-care-procedures(39554aa7-cfb4-41e6-81bd-a522ccf1d851).html.
Pełny tekst źródłaAlderson, Dorothea Priscilla. "Informed consent : problems of parental consent to paediatric cardiac surgery". Thesis, Goldsmiths College (University of London), 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.702485.
Pełny tekst źródłaScott, John. "Informed consent and respect for autonomy". Thesis, University of Sunderland, 2007. http://sure.sunderland.ac.uk/3561/.
Pełny tekst źródłaBullock, Emma Cecelia. "Informed consent and justified hard paternalism". Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/3400/.
Pełny tekst źródłaWalker, 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.
Pełny tekst źródłaSchool of Nursing
Ahmed, Abdul-Kareem H. "SIGN HERE : informed consent in personalized medicine". Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/83832.
Pełny tekst źródłaVita. Cataloged from PDF version of thesis.
Includes bibliographical references (pages 27-30).
The next era of medicine will be one of personalization, scientists and physicians promise. Personalized medicine is a refined clinical approach in which clinicians will utilize your genomic information to help you prevent disease, and tailor targeted therapies for you when you fall ill. This is the future science has slowly been approaching. However, the human genome is not enough, not unless we can decipher its language. One ambitious study to this effect is the Personal Genome Project, led by Dr. George Church at Harvard Medical School. This project will eventually recruit 100,000 volunteers to donate their genomes and a full body of information concerning their biological health. With this data, Church hopes others can cross-analyze these profiles and better determine the role in disease of each gene of the human genome. However, the Personal Genome Project is as much a study in the ethical, legal and social aspects of genomic studies as it is an effort toward personalized medicine. Church envisions a future where privacy cannot be guaranteed. Society is becoming more open and technology is more invasive than ever. Considering this, Church has informed his participants that their information will likely not remain anonymous. With their fully informed consent, he has in turn made all this data public, to promote open science. This ethical approach raises several important questions about expansive genomic studies. The scientific community will have to decide on an approach that will eventually deliver personalized medicine. On one end of the spectrum, there is Church's open approach, and the other, more security, more firewalls and more legislation. In order for personalized medicine to become a reality, society will have to prepare itself for our ever-changing ethical, technological and scientific landscape.
by Abdul-Kareem H. Ahmed.
S.M.in Science Writing
Carr, Kelly Marie. "The Impact of Verbal Explanation and Modified Consent Materials on Orthodontic Informed Consent". The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1298904481.
Pełny tekst źródłaMoloi, Gaotswake Patience. "Informed consent : communication and miscommunication in clinical trials". Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/20157.
Pełny tekst źródłaENGLISH ABSTRACT: Background Informed Consent (IC) has been proposed as the optimal method for ensuring the ethical entry of patients into clinical trials. IC is a vital part of the research process and as such entails more than obtaining a signature on a form. The IC must be given freely, without coercion, and must be based on a clear understanding of what participation involves. Aim The overall aim of this study was to attain an understanding of participants' knowledge regarding informed consent when participating in a research project. Methods The study was conducted at two public hospitals in a city in the Eastern Cape Province of South Africa. The quantitative study used descriptive survey design. A self administered questionnaire was used as a tool for data collection. Results The sample size consisted of 170 women with an average of 25.9 years. The majority had completed secondary level education. More than half of the participants did not have knowledge of the purpose of the original study. The majority of participants did not have knowledge of their responsibilities. Forty-two percent gave uninformative responses and 26% indicated they did not know their responsibilities. None of the participants understood the concept of randomization. The majority (85.9%) of participants indicated that information provided on the IC forms was sufficient for them to decide to participate. Conclusion Despite extensive efforts to ensure that participants understood their participation in the original studies, this study found poor recall of vital information for IC. A signed informed consent does not guarantee that participants understand information given. Recommendations The existing methods of communicating and obtaining of an informed consent seem to be insufficient for participants to make an informed decision. A new approach with more interactive features such as combination of audio-visual techniques might increase the possibilities of the understanding.
AFRIKAANSE OPSOMMING: Agtergrond Ingeligte toestemming (IT) is voorgestel as die optimale metode om die etiese toelating van die pasiënte vir kliniese toetse te verseker. IT is 'n belangrike deel van die navorsingsproses en as sodanig behels dit meer as die verkryging van 'n handtekening op 'n vorm. Die IT moet vrylik gegee word, sonder dwang en moet gebaseer wees op 'n duidelike begrip van wat die deelname behels. Doel Die algemene doel van hierdie studie is om 'n begrip van die deelnemers se kennis met betrekking tot ingeligte toestemming te bepaal, wanneer hulle deelneem aan 'n navorsingsprojek. Metodes Die studie is uitgevoer by twee openbare hospitale in ’n stad in die Oos-Kaap in Suid-Afrika. Die navorsingsontwerp is beskrywend van aard en ’n kwantitatiewe benadering is toegepas. ‘n Self-geadministreerde vraelys is as 'n instrument gebruik om data in te samel. Resultate Die steekproefgrootte het bestaan uit 170 vroue met 'n gemiddelde ouderdom van 25.9 jaar. Die meerderheid van die vroue het opleiding tot op sekondêre vlak. Meer as die helfte van die deelnemers het geen kennis van die doel van die oorspronklike studie gehad nie. Die meerderheid van die deelnemers het ook nie kennis van hul verantwoordelikhede gehad nie. Twee-en-veertig persent het nie toepaslike antwoorde gegee nie en 26% het aangedui dat hulle nie weet wat hul verantwoordelikhede in die studie is nie. Nie een van die deelnemers het die konsep van verewekansiging verstaan nie. Die meerderheid (85.9%) van die deelnemers het aangedui dat die inligting wat deur die IT verskaf word voldoende was om te besluit of hulle aan die studie wou deelneem. Gevolgtrekking Ten spyte van uitgebreide pogings om te verseker dat deelnemers hulle deelname verstaan het in die oorspronklike toetsing, het hierdie studie die swak herroeping van belangrike inligting aangaande IT bewys. ‘n Ondertekende ingeligte toestemming gee geen waarborg dat die deelnemers die inligting waarvoor toestemming geteken is, verstaan nie. Aanbevelings Die bestaande metodes van die kommunikasie en verkryging van ingeligte toestemming blyk onvoldoende te wees om deelnemers ingeligte besluite te laat neem. ‘n Nuwe benadering met meer interaktiewe eienskappe soos ’n kombinasie van oudio-visuele tegnieke mag die moontlikhede om te verstaan, meer duidelik maak.
Książki na temat "Informed consent"
Wear, Stephen. Informed Consent. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-015-8122-6.
Pełny tekst źródłaVictoria, Law Reform Commission of. Informed consent. [Melbourne: The Commission], 1987.
Znajdź pełny tekst źródłaFix, R. M. Informed consent. Orange Park, FL: Frontline Pub. Co., 2007.
Znajdź pełny tekst źródłaByrne, John A. Informed consent. New York: McGraw-Hill, 1996.
Znajdź pełny tekst źródłaCarmi, Amnon. Informed consent. Redaktor UNESCO Chair in Bioethics at the University of Haifa. Haifa, Israel: Israel National Commission for UNESCO, 2003.
Znajdź pełny tekst źródłaCopyright Paperback Collection (Library of Congress), red. Informed consent. New York: New American Library, 1986.
Znajdź pełny tekst źródłaCorsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.
Znajdź pełny tekst źródłaFan, Ruiping, red. Family-Oriented Informed Consent. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-12120-8.
Pełny tekst źródłaCorsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.
Znajdź pełny tekst źródłaCorsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.
Znajdź pełny tekst źródłaCzęści książek na temat "Informed consent"
ten Have, Henk, i Maria do Céu Patrão Neves. "Consent, Informed Consent". W Dictionary of Global Bioethics, 351–52. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-54161-3_171.
Pełny tekst źródłaRieske, Robert D., Stephanie C. Babbitt, Joe H. Neal i Julie A. Spencer. "Informed Consent". W Handbook of Treatments for Autism Spectrum Disorder, 67–84. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61738-1_5.
Pełny tekst źródłaFox, Anthony W. "Informed Consent". W Principles and Practice of Pharmaceutical Medicine, 79–83. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444325263.ch8.
Pełny tekst źródłaAnnas, George J. "Informed Consent". W The Rights of Patients, 83–103. Totowa, NJ: Humana Press, 1992. http://dx.doi.org/10.1007/978-1-4612-0397-1_6.
Pełny tekst źródłaStanton-Jean, Michèle, Hubert Doucet i Thérèse Leroux. "Informed Consent". W Handbook of Global Bioethics, 737–53. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-2512-6_117.
Pełny tekst źródłaCarey, Eileen, i Ruth Ryan. "Informed Consent". W Handbook of Intellectual Disabilities, 221–45. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-20843-1_14.
Pełny tekst źródłaKraushar, Marvin F. "Informed Consent". W Risk Prevention in Ophthalmology, 65–75. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-73341-8_7.
Pełny tekst źródłaDeFabrique, Nathalie. "Informed Consent". W Encyclopedia of Clinical Neuropsychology, 1807–8. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_994.
Pełny tekst źródłaDunn, Laura B., i Laura Weiss Roberts. "Informed Consent". W Encyclopedia of Women’s Health, 649–51. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_217.
Pełny tekst źródłaMallia, Pierre. "Consent: Informed". W Encyclopedia of Global Bioethics, 1–9. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-05544-2_120-1.
Pełny tekst źródłaStreszczenia konferencji na temat "Informed consent"
Utz, Christine, Martin Degeling, Sascha Fahl, Florian Schaub i Thorsten Holz. "(Un)informed Consent". W CCS '19: 2019 ACM SIGSAC Conference on Computer and Communications Security. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3319535.3354212.
Pełny tekst źródłaKulhawy, Darlene, i Alberta Edmonton. "Informed consent? Or is it?" W 1st Annual Worldwide Nursing Conference (WNC 2013). Global Science and Technology Forum Pte Ltd, 2013. http://dx.doi.org/10.5176/2315-4330_wnc13.18.
Pełny tekst źródłaTownsend, Daphne. "Informed Consent in Biomedical Research". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.260448.
Pełny tekst źródłaTownsend, Daphne. "Informed Consent in Biomedical Research". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.4398348.
Pełny tekst źródłaSterling, S. Revi, i Nimmi Rangaswamy. "Constructing informed consent in ICT4D research". W the 4th ACM/IEEE International Conference. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/2369220.2369264.
Pełny tekst źródłaHenley, Jessica, i Simon Kirby. "Robotic Surgery – Implications for Informed Consent". W The Hamlyn Symposium on Medical Robotics: "MedTech Reimagined". The Hamlyn Centre, Imperial College London London, UK, 2022. http://dx.doi.org/10.31256/hsmr2022.17.
Pełny tekst źródłaGrobler, Jan Harm Fouche. "Practical Application of Free Prior Informed Consent". W SPE International Conference and Exhibition on Health, Safety, Security, Environment, and Social Responsibility. Society of Petroleum Engineers, 2018. http://dx.doi.org/10.2118/190574-ms.
Pełny tekst źródłaAlshevsky, Vladimir. "Problems of informed consent in domestic medicine". W Issues of determining the severity of harm caused to human health as a result of the impact of a biological factor. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/conferencearticle_5fdcb03a27a5f7.62532593.
Pełny tekst źródłaLuger, Ewa, i Tom Rodden. "An informed view on consent for UbiComp". W UbiComp '13: The 2013 ACM International Joint Conference on Pervasive and Ubiquitous Computing. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2493432.2493446.
Pełny tekst źródłaVallance, Shirley, Julie Potter, Anne O'Connor, Bridget O'Bree, Dorrilyn Rajbhandari, Ellen McDonald, Andrea Tkaczyk i in. "Informed Consent For An International Thromboprophylaxis Trial". W American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6046.
Pełny tekst źródłaRaporty organizacyjne na temat "Informed consent"
Santos, Elsa, Silvia Llaguno i Ricardo Vernon. Mexico: Protecting informed consent. Population Council, 1999. http://dx.doi.org/10.31899/rh4.1190.
Pełny tekst źródłaHamilton, Leslie. Defining and obtaining informed consent. BJUI Knowledge, sierpień 2019. http://dx.doi.org/10.18591/bjuik.0359.
Pełny tekst źródłaDeborah Schrag, Deborah Schrag, Andrea Andrea Enzinger, Christine Cronin i Jennifer Wind. Improving Informed Consent for Palliative Chemotherapy. Patient-Centered Outcomes Research Institute® (PCORI), sierpień 2019. http://dx.doi.org/10.25302/7.2019.ce.13046517.
Pełny tekst źródłaBertalan, Margit. What is Free, Prior and Informed Consent (FPIC)? Wildlife Conservation Society, 2021. http://dx.doi.org/10.19121/2021.report.45032.
Pełny tekst źródłaMcGrory, Elizabeth, Barbara Friedland, Cynthia Woodsong i Kathleen MacQueen. Informed Consent in HIV Prevention Trials: Report of an International Workshop. Population Council, 2006. http://dx.doi.org/10.31899/hiv1.1021.
Pełny tekst źródłaDickert, Neal, Andrea Mitchell, Candace Speight, Michael Frankel, Sara Goldkind, Yi-An Ko, Raul Nogueira i in. Understanding and Improving Informed Consent for Clinical Trials during Health Emergencies. Patient-Centered Outcomes Research Institute (PCORI), wrzesień 2020. http://dx.doi.org/10.25302/09.2020.me.140210638.
Pełny tekst źródłaBiesecker, Barbara, Melissa Raspa, Douglas Rupert, Rebecca Moultrie, Robert Furberg i Lauren A. McCormack. Making Clinical Trials More Patient-Centered Using Digital Interactive E-Consent Tools. RTI Press, październik 2019. http://dx.doi.org/10.3768/rtipress.2019.op.0063.1910.
Pełny tekst źródłaFriedland, Barbara, Louis Apicella, Katie Schenk, Meredith Sheehy i Paul Hewett. Evaluation of the informed consent process for male circumcision scale-up in Swaziland. Population Council, 2011. http://dx.doi.org/10.31899/hiv1.1012.
Pełny tekst źródłaWood, Susan, Barbara Friedland i Elizabeth McGrory. Informed consent: From good intentions to sound practices—A report of a seminar. Population Council, 2002. http://dx.doi.org/10.31899/rh5.1004.
Pełny tekst źródłaJudith, Meyer, i David Keller. H - Requirement No. 1. OceanNETs, wrzesień 2020. http://dx.doi.org/10.3289/oceannets_d10.1.
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