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Beautiful sacred souls! Welcome back to another episode! Today we have a good chat for these odd and transformative days that we are in! We talk discernment, consent, navigating these days and so much more. Thank you all for being here with us. We are learning our new flow of scheduling and working together, and we expect to have two episodes weekly for the podcast, which are also now on our youtube channel if you'd like to watch the convo instead of just listening. We also have worked out our audio challenges! We love you all so much and wish you all the most benevolent, graceful experience of awakening. With tremendous love, Ivy & Kimberly Watch this episode on YouTube HERE ! Email us at [email protected] Instagram: @inspired.sovereignty Telegram: @inspiredsovereignty & @soulfrens Please SUBSCRIBE to our YouTube channel https://www.youtube.com/channel/UClWyrCHj82O9ACLQ75Dc8Fg Thank you for donations. They help all our creations manifest. Thank you. Venmo: -------------------------------------- Disclaimer: This podcast and the words, conversations, guests, and resources shared are intended to support, encourage, inform and expand thinking to increase self responsibility. Nothing created or shared here is ever intended to diagnose, prescribe, treat or cure. Everyone's health is their own responsibility, and everyone is empowered to exercise wise discernment, educate themselves, ask amazing questions, and seek accurate information and practice informed consent. Always seek a medical or health professional that you trust when you need to. Your body. Your mind. Your soul. Your choice. Your consent. Your authority. You are god, you are sovereign, you are free. And so it is. --- This episode is sponsored by - Anchor: The easiest way to make a podcast. https://anchor.fm/app --- Send in a voice message: https://anchor.fm/inspiredsovereigntyradio/messageSupport this podcast: https://anchor.fm/inspiredsovereigntyradio/support

This study investigates the current state of informed consent practices in clinical trials that integrate artificial intelligence (AI), with a focus on identifying ethical gaps and advancing patient-centered transparency. As AI technologies become increasingly embedded in clinical research—ranging from diagnostic support to data analysis—the adequacy of informed consent documents in communicating AI-specific risks and processes remains critically underexamined. Despite growing ethical concerns around algorithmic bias, data privacy, and patient autonomy, there is a lack of large-scale, empirical assessment of how these issues are addressed in real-world consent procedures. The purpose of this research is to evaluate the transparency, comprehensibility, and ethical rigor of informed consent documents across AI-integrated clinical trials globally. Using a systematic review methodology and a hybrid analytical framework grounded in established ethical models, the study assesses how well these documents disclose AI functionality, associated risks, data governance practices, and participant agency. Special attention is given to the influence of regional regulatory environments and risk stratification in shaping consent quality. The expected outcome of this work is the development of a new framework to standardize and enhance informed consent in AI-driven research. Additionally, the project advocates for the adoption of dynamic digital consent platforms that support ongoing participant engagement, granular data control, and adaptive communication as AI systems evolve. By promoting regulatory harmonization, clinician education, and algorithmic accountability, this research aims to transform informed consent from a static procedural requirement into a living, ethically robust process that upholds patient trust and autonomy in the age of artificial intelligence.

This article is from PLoS ONE , volume 9 . Abstract Verifying participant comprehension continues to be a difficult ethical and regulatory challenge for clinical research. An increasing number of articles assessing methods to improve comprehension have been published, but they use a wide range of outcome measures including open-ended, closed-ended, and self-perceived measures of comprehension. Systematic comparisons of different measures have rarely been reported. This study evaluated the likely direction of bias observed when using open-ended, closed-ended, and perceived ease of comprehension measures among women administered a mock informed consent process in Mwanza, Tanzania. Participants were randomized to either a closed-ended or an open-ended assessment of comprehension, administered the consent process for a hypothetical HIV prevention trial in Kiswahili, and then administered a comprehension assessment, per their randomization. They were then asked how easy or hard it was to understand each of the informed consent components measured in the comprehension assessment. Women in the closed-ended arm had significantly higher overall comprehension scores than in the open-ended arm. Perceived scores were significantly higher when compared to both open-ended and close-ended scores within arms but were similar between arms. Findings highlight the importance of comprehension assessments in complex clinical trials that go beyond asking participants if they understand or have any questions. They also indicate the need for continued exploration of objective measures of comprehension in international clinical research settings, so that points in need of clarification can be efficiently and effectively identified and addressed. Such measures would reduce burdens on both staff and participants that result from well-intentioned but potentially unnecessary time spent explaining in unwarranted detail things already understood.

The left will fight to the death. Everything they can throw is being tossed. There is open discussion of the coming coup. Here is the gateway to private contractors. Huge evidence shows that they run the world. There is a groundswell that is unseen. The coms to the traitors have been discovered. Bank accounts and phone calls can tell a lot. They built all the biggest myths. Stay frosty because we know their plans. Learn more about your ad choices. Visit megaphone.fm/adchoices

In this episode of the Silent War - A new whistleblower emerges from Dominion. Vaccine Mandates are beginning in The United States. Medical professionals world wide are violating medical ethics standards by failing informed consent requirements per one study, and the DOJ is threatening auditors with jail time for audits using civil rights anti racism laws. Also, section 230 may soon be a moot point, as Dr. Shiva has discovered a MASSIVE new bombshell: Democrats in Government were colluding with Big Tech to censors political opponents - this is 1st amendment territory now! Was our platform also shut down, not by the big tech censor, but by President Trump's political rivals? Do not miss this action packed episode.All of this, and much more.For breaking news from one of the most over the target and censored names in the world join our 100% Free newsletter at www.NemosNewsNetwork.com/newsAlso follow us at Gabhttps://gab.com/nemosnewsnetworkNemos News is 100% listener funded. Thank you for your support in our mission to Break the Cycle of Fake News.If you value our work please consider supporting us with our vetted patriot sponsors!www.NemosNewsNetwork.com/sponsorsShop Patriot & Detox the Deep State with www.RedPillLiving.com, Home of Sleepy Joe - the world's most powerful all natural sleep formula & The Great Awakening Gourmet Coffee for Patriots."Our Specialty, is Waking People Up."Other LinksJoin our Telegram chat: www.NemosNewsNetwork.com/chat

Female sterilization is an irreversible form of contraception that was first used in the 19th century and has developed popularity since. Whilst female sterilization is a choice for some women, other unfortunate women find themselves coerced into the option. There have been several reports of this problem dating back from World War II, whereby women are forced to sterilise or the procedure is even done without their knowledge for several reasons. Human rights as stipulated by the World Health Organization (WHO) as well as the South African constitution are protective of female rights to reproduction and their bodies. One of the ethical principles in the practice of medicine is autonomy, the right to self-governance. Forced and coerced female sterilisation does not only violate their human rights, which is a criminal act, but also their right to exercise autonomy. Informed consent is an essential tool that can be used to eliminate allegations of forced or coerced medical procedure when is obtained correctly with patient given full information on the procedure, right to refuse, benefits, consequences and other options available to them. There have been ongoing reports and medico-legal claims on forced female sterilisation both globally and locally. In South Africa, there is currently a case still under investigation where women living with Human Immunodeficiency Virus (HIV) in Gauteng and Kwa-Zulu Natal have reported forced sterilisation to the Health Professions Council of South Africa (HPCSA). This scoping review will look into current practices for consent for sterilisation as well available tools that are currently utilised globally and locally to improve the consent process for female sterilisation. The proposed scoping review will be guided by the enhanced version of Arksey, H., and O’Malley’s scoping review framework and Levac et al 2010 recommendations. We will conduct a comprehensive keyword search for relevant studies published between January 2000 and December 2021, on forced or coerced female sterilisation, issues pertaining to consent process for sterilisation as well as any tools that were developed to improve the consent process for female sterilisation globally from PubMed, Google Scholar, EBSCOhost (Academic search complete, CINAHL, MEDLINE) and Web of Science (WoS) databases. In addition, we will search for relevant grey literature from university repositories as well as international organizations such as the World Health Organization (WHO). We will present the results of the review using the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-analysis: Extension for Scoping Review). We will employ AtlasTi software package to extract the relevant outcomes from the included articles using content thematic analysis. We will conduct quality appraisal of the included articles using the mixed methods appraisal tool (MMAT) version 2018. It is anticipated that the results of the proposed study will inform future research and reveal useful information to guide clinicians counselling women on sterilisation.

Perma.cc archive of https://www.coloradoindependent.com/2010/05/04/colorados-new-informed-consent-bill-celebrated-as-tool-to-fight-racial-profiling/ created on 2022-03-10 21:49:02.827486+00:00.

This article is from Journal of Family Medicine and Primary Care , volume 3 . Abstract Progress in health care technologies has enabled patients to be better informed about all aspects of health care. Patients' informed consent is a legal regulation and a moral principle which represents patients' rights to take part in the clinical decisions concerning their treatment. With increasing awareness among the patients, the concept of informed consent is also evolving in developing countries like India. It is important for the medical and dental practitioners to have a written and signed informed consent from their patients before performing any invasive or irreversible procedures. Informed consent is also needed when providing medical care to children, foreign patients, and incorporating images of the patients while conducting medical and dental research. The present review addresses some of the vital issues regarding informed consent when providing medical and dental care with current review of the literature.

This article is from Journal of Family Medicine and Primary Care , volume 3 . Abstract Progress in health care technologies has enabled patients to be better informed about all aspects of health care. Patients' informed consent is a legal regulation and a moral principle which represents patients' rights to take part in the clinical decisions concerning their treatment. With increasing awareness among the patients, the concept of informed consent is also evolving in developing countries like India. It is important for the medical and dental practitioners to have a written and signed informed consent from their patients before performing any invasive or irreversible procedures. Informed consent is also needed when providing medical care to children, foreign patients, and incorporating images of the patients while conducting medical and dental research. The present review addresses some of the vital issues regarding informed consent when providing medical and dental care with current review of the literature.

this scoping review aims to explore the use, effectiveness, and challenges of eConsent tools, mapping existing evidence and identifying gaps in the literature. We want to have documents available on the oral delivery of informed consent.

In this scoping review, we aimed to (1) Identify the physician-facing decision support tools used in the surgical informed consent process (2) Assess what patient-centered domains are measured by these tools (3) Determine whether the tools are available for older adults and for use in various settings (emergent and elective procedures) (4) Characterize the domains that future tools should measure.

One of St Lukes four pillars is integrity. Forcing a medical product on employees and vendors violates informed consent and integrity. My Job as a Provider is to respect Patients Freedom & Medical Choices. Informed consent is the bedrock for medical freedom. Our healthcare practitioners as well as those vendors who support the hospital and allow it to function are being mandated to take a product that is not proven safe for the long term. "Just to clarify, I am not anti-vaccine, we are pro-health freedom and the ability to choose what is injected into your body." Join Health Freedom Idaho www.healthfreedomidaho.org #stopthemandate #takeastand

Jefferey Jaxen summarises the Informed Consent process in Ireland [02/09/2016]. We also hear from the public health doctor who runs the immunisation program in Ireland.

This film explains the process by which a patient, who has experienced sexual violence, may provide or withdraw permission to proceed with a forensic medical evaluation before, during, or after the medical exam. This film is intended to be screened for the patient. This film has been produced by the Program on Sexual Violence in Conflict Zones at Physicians for Human Rights and it is intended to complement the training workshops the program convenes for medical, law enforcement, and legal professionals on the collection and documentation of forensic evidence of sexual violence. (English version) For more: http://physiciansforhumanrights.org/issues/rape-in-war/program-on-sexual-violence-in-conflict-zones.html Qu'est-ce que le consentement éclairé? https://youtu.be/K0X084gQ09I Ruhusa ama ridhaa? https://youtu.be/gnzcLop4Fdg

PW Rumble Account: https://rumble.com/c/c-741735 PW Twitter Account: https://twitter.com/PWestoff PW Patreon Account: https://www.patreon.com/user?u=653197... HSA Vax Video: https://twitter.com/UKHSA/status/1709495146792824976 ONS Birth Data: https://www.ons.gov.uk/peoplepopulationandcommunity/birthsdeathsandmarriages/livebirths/bulletins/birthsummarytablesenglandandwales/previousReleases

Are Health Care Quality Measures Endangering Informed Consent? In this video, Michelle Cotterman, RN, President of Ohio Advocates for Medical Freedom, discusses informed consent and how policies are endangering it and, thus, our human and civil rights. The reality is that more and more, mandatory vaccination policies are being put in place in the workplace and the community. This idea of informed consent is well established by the Nuremburg Code, the Universal Declaration on Bioethics and Human Rights, Ohio Revised Code 2317.54, and the major medical organizations (AMA, AAP, etc.). These oppressive policies threaten the very ideals expressed and guaranteed in these documents, as well as our U.S. and state Constitutions. It is time to put an end to the encroaching rules, policies, and laws that seek to take away our informed consent! Donate today at www.ohioamf.org/donate. Join us in working to restore and protect medical freedom and informed consent in Ohio and help us become a shining example to the nation! More about hospital quality measures and how they are calculated: https://www.medicare.gov/hospitalcompare/linking-quality-to-payment.html https://s3.amazonaws.com/assets.fiercemarkets.net/public/004-Healthcare/StrRtg_Dec_QtrUpdtSpecRpt.pdf

WATCH FULL HERE: https://youtu.be/vTsebWFLFdc SUPPORT OUR WORK https://www.judicialwatch.org/donate/thank-youtube/ VISIT OUR WEBSITE http://www.judicialwatch.org

This article is from Journal of Public Health Research , volume 2 . Abstract Abstract: Background: The Center for Transfusion Medicine, Cell Therapy and Cryobiology, Milan, Northern Italy, is the headquarter of the POLI-MI biobank. It co-ordinates the biobank activities of the Fondazione Ca’ Granda Ospedale Maggiore Policlinico of Milan. Such activities require specific safeguarding of donors’ rights and protection of sensitive and genetic data. The Fondazione Ca’ Granda Ospedale Maggiore Policlinico has set up a project on informed consent with the aim of developing awareness and understanding of this issue. Within this project, it has been decided to evaluate how consent for biobanking material is expressed. Design and methods: The aim of the study was to evaluate the quality and completeness of consent to biobanking in the POLI-MI biobank. This was a retrospective study carried out in 2012 on samples of consent declarations collected by biobank units in 2011. Some units used a single, standard consent model available from a previous POLI-MI biobank workgroup. Other units used models which had been previouly formulated. Evaluation was made using a form that indicated the essential elements of consent. Results: A total of 48 consent declarations were collected using the single, standard model and 84 were collected using other models. The consent declarations that used the single, standard model were found to be the most complete and were filled in better than other models. Conclusions: Progressive adoption of a simple, standard consent model is expected to improve the quality of consent acquisition. Regular audit of the compliance of consent practices with ethical and legal requirements is mandatory to improve the quality of research biobanking.

This article is from Journal of clinical research & bioethics , volume 5 . Abstract Background: International guidelines recommend the use of appropriate informed consent procedures in low literacy research settings because written information is not known to guarantee comprehension of study information. Objectives: This study developed and evaluated a multimedia informed consent tool for people with low literacy in an area where a malaria treatment trial was being planned in The Gambia. Methods: We developed the informed consent document of the malaria treatment trial into a multimedia tool integrating video, animations and audio narrations in three major Gambian languages. Acceptability and ease of use of the multimedia tool were assessed using quantitative and qualitative methods. In two separate visits, the participants’ comprehension of the study information was measured by using a validated digitised audio questionnaire. Results: The majority of participants (70%) reported that the multimedia tool was clear and easy to understand. Participants had high scores on the domains of adverse events/risk, voluntary participation, study procedures while lowest scores were recorded on the question items on randomisation. The differences in mean scores for participants’ ‘recall’ and ‘understanding’ between first and second visits were statistically significant (F (1,41)=25.38, p

This article is from Trials , volume 14 . Abstract None

GPO Item#:    0575 SuDoc#:     AE 2.110:112-258 Description: An Act To amend section 2710 of title 18, United States Code, to clarify that a video tape service provider may obtain a consumer’s informed, written consent on an ongoing basis and that consent may be obtained through the Internet. This Act may be cited as the "Video Privacy Protection Act Amendments Act of 2012". 126 STAT. 2414; PUBLIC LAW 112-258—JAN. 10, 2013. Shipping List : 2013-0176-p Shipped:     5/3/2013 Stamped:    5/3/2013 GPO PURL:    http://purl.fdlp.gov/GPO/gpo34851 URL: https://www.govinfo.gov/content/pkg/PLAW-112publ258/pdf/PLAW-112publ258.pdf GPO Catalog URL: https://catalog.gpo.gov/F/?func=direct&doc_number=000893748&local_base=GPO01PUB WITHDRAWN FROM HPL COLLECTION

ICF UV IRB

Introduction: A properly-designed informed consent form could help in the use and preservation of relevant information as well as enrich the worth of patient-physician dealings. This research sought to find out if informed consent forms used in health facilities in Benin City, Edo State contained the essential elements of informed consent. Methods: The study was carried out in 38 health facilities (3 public health facilities, and 35 private health facilities) in Benin City, the administrative headquarter of Edo State, South-south, Nigeria. A checklist was utilized to appraise informed consent documents used in these health facilities to determine their adequacy in terms of the critical elements contained in it. The checklist was developed based on the contents of the prototype form (proforma) provided by the Medical and Dental Council of Nigeria (MDCN). The checklist consisted of “Yes” and “No” sections corresponding to the 16 items considered necessary for valid consent documentation. Results: None of the consent forms in public health facilities had a notation that the benefits of proposed management or procedure were clarified, that the patient clearly understood the language of presentation or that the choice to ruminate on the procedure for a while prior to giving assent was offered to the patient. Only 11.4% of forms examined in private health facilities had a notation that the benefits and risk of the intended management option or procedure were explained to the patient. Conclusion: Many consent forms currently in use in health facilities in Benin City did not wholly adopt the contents of the proforma provided by the MDCN. Most informed consent documents examined in this study lacked the essential elements of informed consent. 

Perma.cc archive of https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543760/ created on 2022-08-08 15:25:35.187749+00:00.

The recent unethical COVID-19 informed consent in Bangladesh focuses on the weakness of the unethical healthcare system in this country. After 50 years when Bangladesh celebrated its Golden Jubilee of independence, the Corona crisis opened our eyes once again - how weak the countries’ policymaking system is! We try to figure out the ethical gap of the corona vaccines’ informed consent which is used by the government of Bangladesh.

Guest Chris Downey, founder and Director of VaxCalc Labs -- "the informed consent technology company" -- discusses how the tools available at VaxCalc help parents and individuals make scientifically and ethically sound fully-informed vaccination decisions. Reference Links https://informedchoicewa.substack.com/ https://vaxcalc.org/

Guest Chris Downey, founder and Director of VaxCalc Labs -- "the informed consent technology company" -- discusses how the tools available at VaxCalc help parents and individuals make scientifically and ethically sound fully-informed vaccination decisions. Reference Links https://informedchoicewa.substack.com/ https://vaxcalc.org/

Physicians for Informed Consent (PIC) is a 501(c)(3) educational charity launched on July 1, 2016--the day California's new mandatory vaccination law (SB277) went into effect. This launch video features the story of PIC's founding members, advisors, and directors, and was first shown live at PIC's Inaugural Meeting and Luncheon on March, 12, 2017 in Costa Mesa, CA. Help us change the cultural acceptance of mandatory vaccination laws. Donate today! https://physiciansforinformedconsent.org/donate Learn how donation cards work: https://support.google.com/youtube/?p=donate_FAQ

Moms for Liberty-Sarasota County's Vice-Chair, Teresa DeWitt, reads the shocking UNITE US Informed Consent to the School Board. Find UNITE US Consent Form Here: https://scs.novusagenda.com/agendapublic/CoverSheet.aspx?ItemID=2899&MeetingID=1065

Het vaccine van Jansen levert blanco bijsluiter. Mensen mogen alleen worden geënt als er sprake is van ‘informed consent’. Dit maakt het middel verboden te verwerken voor zorg medewerkers.

http://tinyurl.com/AVDcard -- the trustees of the Natural Solutions Foundation urge all to assert their right to Informed Consent as against the proposed CDC Quarantine & Treatment (Vaccination) regulation that seeks override consent. More here: http://tinyurl.com/InformedConsentProtection

Show Notes: http://www.libertyweekly.net/187 Buy "Consent is Morality:" https://paxdeals.com/products/consent-is-morality (Use promo code "liberty" for 30% off an autographed copy) Consent is a concept that is deeply rooted in the principle of self ownership. It is also a concept that progressives, especially those who support COVID totalitariansim, purport to care about. Author Sean Leal joins me to discuss issues of consent at the center of resistance to COVID19 mandates. Sean is the author of the book, "Consent is Morality: A Philosophy of Peace" and has been communicating the ideas of individual liberty for over 10 years, including speaking engagements at state schools on the principles of consent and how government actions violate them. Follow Sean on Facebook, or on Twitter and TikTok @seanofpeace.

This film provides an overview of the key steps for clinicians to follow in order to obtain informed consent from patients before, during, and after a forensic examination for sexual assault. This film is intended to be screened for clinicians. This film has been produced by the Program on Sexual Violence in Conflict Zones at Physicians for Human Rights and it is intended to complement the training workshops the program convenes for medical, law enforcement, and legal professionals on the collection and documentation of forensic evidence of sexual violence. (English version) For more information: http://physiciansforhumanrights.org/issues/rape-in-war/program-on-sexual-violence-in-conflict-zones.html Comment obtenir un consentement éclairé valable? https://youtu.be/Kg1YS6ktwJc Jinsi ya kupata ridhaa yenyi kuwa kalali https://youtu.be/pLmX6vDJzIU

Perma.cc archive of https://www.ictinc.ca/free-prior-informed-consent created on 2021-12-21 05:10:29+00:00.

Perma.cc archive of https://www.ictinc.ca/free-prior-informed-consent created on 2021-12-21 05:10:29+00:00.

A Vermont school injected a student with a COVID-19 shot without parental consent and the state supreme court ruled against the parents. Guest John Klar--attorney, farmer, and author of  Small Farm Republic --discusses the Vermont Supreme Court's decision in Politella v. Windham Southeast School District. Reference Links https://informedchoicewa.substack.com/ https://www.smallfarmrepublic.com/ https://brownstone.org/articles/vermont-supreme-court-sacrifices-children-to-big-pharma/

Guest: Owain Tudor | Director of the company called EIDO. See omnystudio.com/listener for privacy information.

Guest: Owain Tudor | Director of the company called EIDO. See omnystudio.com/listener for privacy information.

This item represents a case in PACER, the U.S. Government's website for federal case data. If you wish to see the entire case, please consult PACER directly.

This item represents a case in PACER, the U.S. Government's website for federal case data. If you wish to see the entire case, please consult PACER directly.

This item represents a case in PACER, the U.S. Government's website for federal case data. If you wish to see the entire case, please consult PACER directly.

This item represents a case in PACER, the U.S. Government's website for federal case data. If you wish to see the entire case, please consult PACER directly.

Informed Consent and Other Cosmic Ironies KiaraSayre Summary: Fun fact: interview-based research typically has to go through ethical review, and while oral histories have generally been exempt, that is less and less the case. Another fun fact: Tim is no longer allowed to fill out paperwork.

Research ethics are of fundamental importance to any research. They define and shape the research process from the very beginning as they are the code on which academics rely on as guiding practice in the field (Hopf, 2004). Informed consent is an interesting concept as it is interwoven with other ethical issues that include power, privacy and anonymity (Punch, 2002). All of these are ongoing concerns for a researcher and can arise at any stage of the research process (Coad & Evans, 2008). This article describes the informed consent process for an in-progress research masters thesis about the school experiences of senior secondary school students who have funding from Ongoing and Reviewable Resource Scheme (ORRS). It examines this in relation to the "hierarchy of gatekeepers" (Powell & Smith, 2009, Stalker, 1998) and issues of capacity to give informed consent.

Research ethics are of fundamental importance to any research. They define and shape the research process from the very beginning as they are the code on which academics rely on as guiding practice in the field (Hopf, 2004). Informed consent is an interesting concept as it is interwoven with other ethical issues that include power, privacy and anonymity (Punch, 2002). All of these are ongoing concerns for a researcher and can arise at any stage of the research process (Coad & Evans, 2008). This article describes the informed consent process for an in-progress research masters thesis about the school experiences of senior secondary school students who have funding from Ongoing and Reviewable Resource Scheme (ORRS). It examines this in relation to the "hierarchy of gatekeepers" (Powell & Smith, 2009, Stalker, 1998) and issues of capacity to give informed consent.

Obtaining informed consent for research with nursing home patients is not only difficult in more ways than one but also raises ethical challenges. Nursing home research has increasingly improved the quality of life of older adults living in nursing homes. Informed consent constitutes the foundational principle of all research, yet there is a lack of explicit guidelines for obtaining consent. Through a synthesis of comprehensive research findings on planning, study recruitment, and ecological factors, this study proposes a best practice approach to obtain genuine informed consent from nursing home patients with decisional capacity. The aforementioned variables are indispensable to sound medical and research ethics, patient dignity, and the corresponding conclusions drawn from such research. A threepronged approach that includes consideration of the nursing home setting, the research design, and recruitment helps to ensure genuine informed consent from older adults who consent to participate in the research. Informed consent, when properly secured and implemented through special considerations, respects the inherent dignity of every patient. This article proposes such a protocol that operationalizes obtaining informed consent from those elderly individuals with decisional capacity. It contributes to the nursing literature and best practices in the nursing home on informed consent. Keywords: Informed consent; Nursing; Decisional capacity; Diagnostic interventions; Clinical trials; Research ethics

This article is from Trials , volume 14 . Abstract None

Perma.cc archive of https://www.ncbi.nlm.nih.gov/books/NBK430827/ created on 2021-12-30 12:06:16+00:00.

Perma.cc archive of https://www.ncbi.nlm.nih.gov/books/NBK430827/ created on 2021-12-30 12:06:16+00:00.

This item represents a case in PACER, the U.S. Government's website for federal case data. If you wish to see the entire case, please consult PACER directly.