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COMMENT AND RESPONSE

Evaluation in health promotion: thoughts from inside a human research ethics committee

Judy Allen A C and Felicity Flack B
+ Author Affiliations
- Author Affiliations

A Faculty of Law, University of Western Australia, 35 Stirling Highway, Crawley, WA 6009, Australia.

B Telethon Kids Institute, University of Western Australia, PO Box 855, West Perth, WA 6872, Australia.

C Corresponding author. Email: judy.allen@uwa.edu.au

Health Promotion Journal of Australia 26(3) 182-185 https://doi.org/10.1071/HE15062
Submitted: 14 June 2015  Accepted: 7 September 2015   Published: 5 November 2015

Abstract

Health promotion research, quality improvement and evaluation are all activities that raise ethical issues. In this paper, the Chair and a member of human research ethics committees provide an insiders’ point of view on how to demonstrate ethical conduct in health promotion research and quality improvement. Several common issues raised by health promotion research and evaluation are discussed including researcher integrity, conflicts of interest, use of information, consent and privacy.


References

[1]  National Health and Medical Research Council. National Statement on Ethical Conduct in Human Research. Canberra: Australian Government; 2007.

[2]  Population Health Research Network. For Researchers. 2011. Available from: http://www.phrn.org.au/for-researchers/introduction/ [Verified 30 September 2015]

[3]  Holman , CD , Bass , J , Rosman , D , Smith , M , Semmens , J , Glasson E, et al (2008) A decade of data linkage in Western Australia: strategic design, applications and benefits of the WA data linkage system. Aust Health Rev 32, 766–77.
A decade of data linkage in Western Australia: strategic design, applications and benefits of the WA data linkage system.Crossref | GoogleScholarGoogle Scholar | 18980573PubMed |

[4]  Adams , C , Allen , J (2014) Government databases and public health research: facilitating access in the public interest. J Law Med 21, 957–72.

[5]  Payne , JM , D’Antoine , H , France , K , McKenzie , A , Henley , N , Bartue A, et al (2011) Collaborating with consumer and community representatives in health and medical research in Australia: results from an evaluation. Health Res Policy Syst 9, 18
Collaborating with consumer and community representatives in health and medical research in Australia: results from an evaluation.Crossref | GoogleScholarGoogle Scholar | 21569591PubMed |

[6]  Fisher , C (2011) Implications of participation and equality in the research process for health promotion practice: domestic violence as an example. Health Promot J Austr 22, 119–23.

[7]  National Health and Medical Research Council. Statement on consumer and community participation in health and medical research. Canberra: Australian Government; 2002.

[8]  Allen , J , Holman , CJD , Meslin , E , Stanley , F (2013) Privacy protectionism and health information: is there any redress for harms to health? J Law Med 21, 473–85.

[9]  National Health and Medical Research Council. Guidelines under Section 95 of the Privacy Act 1988 (Cth). 2000. Available from: http://www.nhmrc.gov.au/_files_nhmrc/publications/attachments/e26.pdf [Verified 1 October 2015].

[10]  National Health and Medical Research Council. Guidelines approved under Section 95A of the Privacy Act 1988 (Cth). 2001. Available from: http://www.nhmrc.gov.au/guidelines-publications/e43 [Verified 1 October 2015].

[11]  Office of the Australian Information Commissioner. Guide to securing personal information ‘reasonable steps’ to protect personal information. Canberra: Australian Government; 2015.