Research involving adults lacking capacity to consent: the impact of research regulation on ‘evidence biased’ medicine-Reference-Cited by-同舟云学术

Research involving adults lacking capacity to consent: the impact of research regulation on ‘evidence biased’ medicine

Published:2016-09-08 Issue:1 Volume:17 Page:
ISSN:1472-6939
Container-title:BMC Medical Ethics
language:en
Short-container-title:BMC Med Ethics

Author:

Shepherd Victoria

Publisher

Springer Science and Business Media LLC

Subject

Health Policy,Health (social science),Issues, ethics and legal aspects

Link

http://link.springer.com/content/pdf/10.1186/s12910-016-0138-9.pdf

Reference30 articles.

1. Head MG, Walker SL, Nalabanda A, Bostock J, Cassell JA. Researching scabies outbreaks among people in residential care and lacking capacity to consent: A case study. Public Health Ethics. Advanced Access published online 16 Apr 2015. doi: 10.1093/phe/phv011 .

2. Helmchen H, Hoppu K, Stock G, Thiele F, Vitiello B, Weimann A. From exclusion to inclusion: Improving clinical research in vulnerable populations. Berlin: Berlin-Brandenburg Academy of Sciences and Humanities. 2014. http://edoc.bbaw.de/volltexte/2014/2592/pdf/BBAW_Vulnerable_Populationen_PDFA1_b.pdf . Accessed 22 June 2015.

3. Lewis K. Participation of people with a learning disability in medical research. Royal Mencap Society. 2014. https://www.mencap.org.uk/sites/default/files/documents/Participation%20of%20people%20with%20a%20learning%20disability%20in%20medical%20_1.pdf . Accessed 6 June 2016.

4. Lott JP. Vulnerable/special participant populations. Developing World Bioethics. 2005;5:31–54.

5. Maas M, Kelle L, Park M, Specht J. Issues in conducting research in nursing homes. West J Nurs Res. 2002;4:373–89.

Cited by 55 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Allocating municipal services to individuals with complex rehabilitation needs – a discourse analysis of individual administrative decision letters;BMC Health Services Research;2024-04-12

2. In-person and remote recruitment of people with dementia into a primary care-based cluster randomised controlled trial: lessons from the Dementia PersonAlised Care Team (D-PACT) feasibility study;2024-02-01

3. Improving the inclusion of an under-served group in trials: development and implementation of the INCLUDE Impaired Capacity to Consent Framework;Trials;2024-01-25

4. Family Conflict in Dementia Caregiving: Maintaining Research Ethics and Integrity;Ethics and Integrity in Research with Older People and Service Users;2023-11-24

5. World Cafés as a participatory approach to understanding research agendas in primary care with underserved communities: reflections, challenges and lessons learned;Research Involvement and Engagement;2023-10-28