A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol

Author:

Berry Jesia G, ,Ryan Philip,Braunack-Mayer Annette J,Duszynski Katherine M,Xafis Vicki,Gold Michael S

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Medicine (miscellaneous)

Reference40 articles.

1. Singleton P, Wadsworth M: Consent for the use of personal medical data in research. BMJ. 2006, 333: 255-258. 10.1136/bmj.333.7561.255.

2. Commonwealth of Australia: National Statement on Ethical Conduct in Human Research. 2007, Canberra: Commonwealth of Australia, http://www.nhmrc.gov.au/publications/synopses/e72syn.htm

3. Williams B, Irvine L, McGinnis AR, McMurdo ME, Crombie IK: When "no" might not quite mean "no"; the importance of informed and meaningful non-consent: results from a survey of individuals refusing participation in a health-related research project. BMC Health Serv Res. 2007, 7: 59-10.1186/1472-6963-7-59.

4. Sommerville A: Commentary: What's wrong with opting out?. BMJ. 2001, 322: 1220-1221.

5. National Health and Medical Research Council: The Impact of Privacy Legislation on NHMRC Stakeholders - Comparative Stakeholder Analysis. 2004, Canberra: NHMRC, http://www.nhmrc.gov.au/about/privacy_regulation.htm

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