Whose risk? Whose responsibility? The Epidemiology of intervening in health risk behaviours for Aboriginal and Torres Strait Islander people
Abstract
This thesis presents a collection of applied epidemiological
studies and is primarily focused on health risk behaviours and
preventive health programs. The studies included:
- a cross-sectional analysis of data from two national Aboriginal
and Torres Strait Islanders surveys. The study examined estimates
of smoking prevalence by Indigenous Regions, 2012/13 and
2014/15;
- a pre- and post- study of a local Aboriginal-developed tobacco
control campaign in Central Australia. The study examined change
in smokers and ex-smokers knowledge, attitude and behaviours to
tobacco use, 2016-17;
- a retrospective cohort study of Aboriginal Community Controlled
Health
Services which examined if outcomes in smoking were associated
with targeted Indigenous tobacco control funding, 2014-2017;
- a clinical audit to identify and provide recommendations to
improve the pathways available to help identified smokers quit,
in six Aboriginal Community Controlled Health Services in
Queensland 2017;
- an evaluation of the Royal Flying Doctors Service Monitoring
System for an obesity-prevention program, the Healthy Living
program, delivered in remote communities in South Australia
2007-2016; and,
- an outbreak investigation of gastroenteritis following
Melbourne Cup luncheons in the Canberra, November 2016.
In all but one study, I examined data availability, collection
and analysis to support program evaluations. Although, Australian
national survey data for the Aboriginal and Torres Strait
Islander population are the most comprehensive source on health
risk behaviours, the data’s utility for evaluating regional
program level activities and campaigns is challenged by small
sizes and data restrictions. In my study of regional smoking
prevalence, I noted that wide confidence intervals meant that
changes over time at a regional level could not be detected.
Further, cross sectional analysis is restricted to comparing
changes in sub-populations, jurisdictions or regions over time
rather than an analysis of changes in individuals over time. As
such, these analyses do not allow the attribution of exposures,
including exploring what program specific activities and
campaigns lead to changes.
In response to the national data limitations, managers and
implementers of individual programs are opting to develop their
own studies, monitoring and evaluation systems. In my pre- and
post- study of smokers in Central Australia, I observed
improvements in participants’ knowledge of smoking health risks
and increased numbers of ex-smokers. I have recommended that next
phase of Australian Government’s Tackling Indigenous Smoking
evaluation needs to better examine which program specific
exposures in tobacco control led to: the de-normalisation of
tobacco use in communities; increased quit attempts; reduced
uptake of smoking; and, the overall declines in smoking
prevalence. I also examined the RFDS Monitoring System, a program
monitoring system established to track changes in participants
due to community-based health promotion activities. Local
surveys/sentinel surveillance and program monitoring can help to
improve program reporting and evaluations, is responsive to local
data requests and builds health service capabilities. However,
the system for ongoing data collection at an individual program
level can also be compromised because of lack of comparability
across sites/activities, limited budget, inadequate definitions
of sampling frames, lack of standard operating procedures for
data collection and the onus on nontechnical staff to analyse
data. Australia needs an enhanced data collection system for
preventive health that supports both local and regional data
needs, while remaining comparable at a national level.
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