Reasons for not participating in PCTs: the comparative case of emergency research under an exception from informed consent (EFIC)

Reasons for not participating in PCTs: the comparative case of emergency research under an exception from informed consent (EFIC)

Bibliografski detalji
Glavni autori:	Sahan, K, Sheehan, M, Cowan, E
Format:	Journal article
Jezik:	English
Izdano:	Taylor and Francis 2023

Slični predmeti

Misuse of "usual care" in emergency care research: a call for adapting rules governing exception from informed consent (EFIC) studies
od: Cowan, E, i dr.
Izdano: (2020)

Community consultation for Exception from Informed consent (EFIC) before and during the COVID-19 pandemic
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Izdano: (2024-02-01)

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od: Paraskevi Dimou, i dr.
Izdano: (2022-04-01)

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od: Elías V de la Rosa Masdueño, i dr.
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PCTS: An Object-Oriented Diagnostic and Trouble-Shooting System for Maintenance of Personal Computers
od: Malhotra, R.
Izdano: (1998-12-01)

Emergency medicine research: rites, rituals and consent.
od: Harston, G, i dr.
Izdano: (2014)

Emergency medicine research: Rites, rituals and consent
od: Harston, G, i dr.
Izdano: (2014)

EFIC 2006 – 5th Congress of The European Federation of IASP® Chapters (EFIC), Istanbul, Turkey, September 13 – 16, 2006. Europe Against Pain, Don’t Suffer in Silence
od: Wartolowska, K, i dr.
Izdano: (2006)

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od: Sumita Trivedi, i dr.
Izdano: (2024-05-01)

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od: Ijudin
Izdano: (2020-02-01)

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od: Amrita Sil, i dr.
Izdano: (2017-01-01)

Capacity to give informed consent to participate in medical research
od: Živojinović Dragica
Izdano: (2014-01-01)

Participant characteristics and reasons for non-consent to health information linkage for research: experiences from the ATHENA COVID-19 study
od: Kim Greaves, i dr.
Izdano: (2024-01-01)

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od: Zlatan Husukić, i dr.
Izdano: (2018-03-01)

COMPARATIVE ANALYSIS OF THE EFICENCY OF POWERPLEX 16 AND POWERPLEX FUSION MULTIPLEX STR KITS IN THE ANALYSIS OF THE CHALLENGING FORENSIC SAMPLES
od: Zlatan Husukić, i dr.
Izdano: (2017-12-01)

Towards an understanding of the ethics of electronic consent in clinical trials
od: Sahan, K, i dr.
Izdano: (2024)

Towards an understanding of the ethics of electronic consent in clinical trials
od: Katherine Sahan, i dr.
Izdano: (2024-08-01)

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od: Evelien De Sutter, i dr.
Izdano: (2022-06-01)

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od: Steven E. Raper, MD, JD, i dr.
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Improving Community Understanding of Medical Research: Audience Response Technology for Community Consultation for Exception to Informed Consent
od: Taher Vohra, i dr.
Izdano: (2014-07-01)

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od: Carlo Petrini
Izdano: (2011-12-01)

Informed consent under ignorance
od: Villiger, D
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od: Silmara Meneguin, i dr.
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od: Bruno Giraudeau, i dr.
Izdano: (2012-01-01)

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od: Rieka Mustika, i dr.
Izdano: (2020-09-01)

Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales.
od: Shepherd, V, i dr.
Izdano: (2019)

Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales
od: Victoria Shepherd, i dr.
Izdano: (2019-04-01)

Can involuntarily admitted patients give informed consent to participation in research?
od: C W van Staden
Izdano: (2007-02-01)

Informed Consent as a Component of Online Research Ethics -- The Perspective of the Participants
od: Nataša B. Matović, i dr.
Izdano: (2021-11-01)

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od: Sheehan, M, i dr.
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Motivation to participate and experiences of the informed consent process for randomized clinical trials in emergency obstetric care in Uganda
od: Dan Kabonge Kaye
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od: Janelle Jackman, i dr.
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Assent is not consent.
od: Sibley, A, i dr.
Izdano: (2012)

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od: A Nienaber
Izdano: (2010-12-01)

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od: John B Holcomb, i dr.
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od: Chou Yiing-Jenq, i dr.
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