Opt-out as an acceptable method of obtaining consent in medical research: a short report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2288
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Opt-out as an acceptable method of obtaining consent in medical research: a short report ; volume:11 ; number:1 ; day:6 ; month:4 ; year:2011 ; pages:1-4 ; date:12.2011
BMC medical research methodology ; 11, Heft 1 (6.4.2011), 1-4, 12.2011
- Creator
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Vellinga, Akke
- Contributor
- DOI
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10.1186/1471-2288-11-40
- URN
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urn:nbn:de:1111-2016032132858
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:49 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vellinga, Akke
- Cormican, Martin
- Hanahoe, Belinda
- Bennett, Kathleen
- Murphy, Andrew W.
- SpringerLink (Online service)
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Forschungsklausel statt Broad Consent : Sekundärnutzung von Patientendaten ohne Einwilligung, dafür mit Opt-out
Obtaining Record Linkage Consent: Results from a Wording Experiment in Germany
Obtaining Record Linkage Consent: Results from a Wording Experiment in Germany
Can obtaining informed consent alter self-reported drinking behaviour? A methodological experiment
A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol
Opt-in vs. Opt-out = opt-in-opt-out? : On the activation of the ICC's jurisdiction over the crime of aggression
Correlates of obtaining informed consent to data linkage: Respondent, interview and interviewer characteristics
Securing recruitment and obtaining informed consent in minority ethnic groups in the UK
Confidence level, challenges, and obstacles faced by orthopedic residents in obtaining informed consent
How clinicians discuss patients’ donor registrations of consent and presumed consent in donor conversations in an opt-out system: a qualitative embedded multiple-case study
Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues
The emerging need for family-centric initiatives for obtaining consent in personal genome research
Forschungsklausel statt Broad Consent : Sekundärnutzung von Patientendaten ohne Einwilligung, dafür mit Opt-out
Obtaining Record Linkage Consent: Results from a Wording Experiment in Germany
Obtaining Record Linkage Consent: Results from a Wording Experiment in Germany
Can obtaining informed consent alter self-reported drinking behaviour? A methodological experiment
A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol
Opt-in vs. Opt-out = opt-in-opt-out? : On the activation of the ICC's jurisdiction over the crime of aggression
Correlates of obtaining informed consent to data linkage: Respondent, interview and interviewer characteristics
Securing recruitment and obtaining informed consent in minority ethnic groups in the UK
Confidence level, challenges, and obstacles faced by orthopedic residents in obtaining informed consent
How clinicians discuss patients’ donor registrations of consent and presumed consent in donor conversations in an opt-out system: a qualitative embedded multiple-case study
Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues