|Home | About | Journals | Submit | Contact Us | Français|
Indigenous Australians are significantly less likely to participate in colorectal cancer (CRC) screening compared to non-Indigenous people. This study aimed to identify important factors influencing the decision to undertake screening using Faecal Occult Blood Testing (FOBT) among Indigenous Australians. Very little evidence exists to guide interventions and programmatic approaches for facilitating screening uptake in this population in order to reduce the disparity in colorectal cancer outcomes.
Interviewer-administered surveys were carried out with a convenience sample (n=93) of Indigenous Western Australians between November 2009-March 2010 to assess knowledge, awareness, attitudes and behavioural intent in regard to CRC and CRC screening.
Awareness and knowledge of CRC and screening were low, although both were significantly associated with exposure to media advertising (p=0.008; p<0.0001). Nearly two-thirds (63%; 58/92) of respondents reported intending to participate in screening, while a greater proportion (84%; 77/92) said they would participate on a doctor’s recommendation. Multivariate analysis with logistic regression demonstrated that independent predictors of screening intention were, greater perceived self-efficacy (OR=19.8, 95% CI=5.5-71.8), a history of cancer screening participation (OR=6.8, 95% CI=2.0-23.3) and being aged 45 years or more (OR=4.5, 95% CI=1.2-16.5). A higher CRC knowledge score (medium vs. low: OR=9.9, 95% CI=2.4-41.3; high vs. low: 13.6, 95% CI=3.4-54.0) and being married or in a de-facto relationship (OR=6.9, 95% CI=2.1-22.5) were also identified as predictors of intention to screen with FOBT.
Improving CRC related knowledge and confidence to carry out the FOBT self-screening test through education and greater promotion of screening has the potential to enhance Indigenous participation in CRC screening. These findings should guide the development of interventions to encourage screening uptake and reduce bowel cancer related deaths among Indigenous Australians.
Indigenous Australians are at greater risk of death following a bowel cancer diagnosis compared to their non-Indigenous counterparts due to higher rates of late stage diagnoses of the disease . Many of these deaths are easily preventable through bowel cancer screening (also known as colorectal cancer (CRC) screening) which can detect bowel cancer in its early stages when the likelihood of successful treatment is high [2,3]. In Australia, a National Bowel Cancer Screening Program (NBCSP) utilising Faecal Occult Blood Testing (FOBT) commenced in 2006 providing free screening to all adults aged 50, 55 and 65 years. Further details and a brief history of the Australian program are described in an earlier review  and summarised in Table Table11.
Regular population screening with the FOBT has been shown to reduce mortality from bowel cancer [15,18,19], however participation rates of Indigenous Australians are less than half that of the general population . These findings parallel CRC screening uptake rates in Indigenous and ethnic minority groups around the world, which are also disproportionately lower than mainstream populations [21-25].
Evidence from other cancer screening programs in Australia indicate that lower participation of Indigenous people results from a multitude of structural, socio-cultural and behavioural factors, including shame and fear regarding cancer, culturally insensitive services, poor literacy, distance and access barriers, and low levels of knowledge and awareness of the cancer, the screening tests available, and associated benefits of screening .
To successfully create targeted messages and educational resources, and to inform interventions aimed at enhancing screening participation, requires understanding of the current knowledge, attitudes and beliefs of the community of interest. To date there have not been any peer-reviewed studies investigating the knowledge and attitudes of Indigenous Australians towards bowel cancer screening, and the factors influencing the decision to engage in screening utilising FOBT.
Determinants of screening participation have been examined in the context of health behaviour theories such as the Health Belief Model  which provides a framework in which to study the relationship between an individual’s perceptions and beliefs about a disease, and their decision of whether to engage in a preventive health behaviour. Perceptions of personal susceptibility to, and perceived severity of the disease, belief in one’s ability to undertake a preventive action (perceived self-efficacy), the potential benefits of, and perceived barriers to undertaking this behaviour, all influence an individual’s decision to partake in a preventive action. Attitudes are also influenced by demographic and other structural or socio-psychological factors. This model purports that a cue to action must occur to trigger a behavioural change; this may result from a doctor’s recommendation, media advertisement or an intervention. Several studies have used health belief theories to understand and identify factors associated with screening compliance [28-31]. By taking a similar approach, this study aimed to elucidate factors that may be associated with CRC screening intention. We present findings from a baseline survey that was conducted as part of an intervention study to assess the current knowledge, attitudes and behavioural intentions of Indigenous Western Australians in relation to bowel cancer and screening with FOBT. This information is critical for identifying specific areas for intervention, and focus for health promotion and education, to improve uptake of CRC screening and reduce disparities in bowel cancer outcomes for Indigenous Australians.
Participants were recruited from two regional and one metropolitan site in Western Australia through community and family networks of health professionals known to the researchers. Recruitment occurred between November 2009-March 2010 with assistance from Aboriginal staff employed in Aboriginal-specific health services. Eligibility criteria included self-identification as Aboriginal or Torres Strait Islander, aged 35 years or more, and the provision of written informed consent prior to participation. Questionnaires were administered at face-to-face interviews and participants received $20 to compensate for time and travel expenses. An Indigenous reference group assisted with all aspects of the study. The Western Australian Aboriginal Human Information and Ethics Committee (250 08/09) and the Curtin University Research Ethics Committee (CIH 11-2009) approved the study.
The questionnaire measured respondent’s knowledge, attitudes, beliefs and behaviours related to the prevention, early detection and treatment of bowel cancer. The instrument was adapted and further developed from surveys identified in relevant literature, as no existing validated questionnaire was found that examined these elements in Indigenous Australians for any cancer screening modality. We favoured items from surveys used with minority and/or Indigenous populations and which were guided by key elements of the Health Belief Model [32,33]. Items were also adapted from the knowledge, attitudes and practices (KAP) survey conducted on the general Australian population prior to the NBCSP pilot . Before implementation, the questionnaire was piloted on a small group of Aboriginal people to ensure understanding and cultural appropriateness, and modified accordingly.
The survey examined awareness of bowel cancer and bowel cancer screening (if they had heard about the disease or the screening test/program and to describe what they knew) and general knowledge and recognition of risk factors and signs and symptoms of bowel cancer. A knowledge score was computed for each respondent based on 18 knowledge items with scores representing the number of correctly answered items. For analysis, scores were divided into tertiles of low (0-11), medium (12-15) and high (16-18). These cut-off points were selected based on dividing our sample population in almost equal thirds so that each third contained roughly the same number of cases. As responses were distributed towards greater knowledge with very few participants having a score less than 6, it was not appropriate to divide the total score based upon being one third of the range (i.e. 0-6, 7-12, 13-18). Respondents in the bottom third were considered to have lowest knowledge, the middle third as medium knowledge, and top third as high knowledge.
Screening behaviour was determined indirectly by asking respondents about their intention to participate in bowel cancer screening (‘Would you consider doing an FOBT bowel cancer screening test in the next 6-12 months if a screening kit was given or sent to you?’), and if they would take up screening following a doctor’s recommendation. Attitude measures included perceptions of personal susceptibility to (‘Do you believe you are at risk of getting bowel cancer?’) and perceived severity of bowel cancer (‘Do you think bowel cancer can be cured if found early?’), perceived self-efficacy (‘How confident do you feel in your ability to do the FOBT screening test?’), perceived benefits, barriers and motivators for bowel cancer screening, fatalistic attitudes (‘Getting cancer is like being sentenced to death’) and perceptions of shame (‘You would feel too ashamed if you found out you had bowel cancer’).
Items presented in a statement format required respondents to indicate whether they agreed or disagreed, with response categories consisting of a five-point Likert scale (1=strongly disagree, 2=disagree, 3=agree, 4=strongly agree, and 5=don’t know). Where the format of the question answer was yes, no or don’t/know, the no and don’t know categories were combined for bivariate and multivariate analyses.
Health-care seeking behaviour including past screening participation and subjective health status were assessed, as was family or personal cancer experience and exposure to media advertising on bowel cancer screening. Socio-demographic information was also collected and included self-rated English reading ability.
Questionnaire data was analysed using statistical software PASW statistics 17 (SPSS Inc., IBM Company, Chicago, Ill., USA). Descriptive statistics were carried out on all survey items. Bivariate analyses were conducted using Chi-square or Fisher’s exact test (when Chi-square assumptions were not met) to examine relationships between categorical variables. Responses were dichotomised as described above for bivariate and multivariate analyses. Binary logistic regression was used to explore the relationship between intention to screen for bowel cancer and variables showing associations at the p=0.30 level or less in bivariate analyses to identify independent predictors of screening intent. All variables showing associations at the p=0.30 level or less were included in the first step of the logistic regression model. Variables with ten or more missing responses were excluded, as was the item measuring awareness that bowel cancer/polyps can be asymptomatic, as this was included in the calculation of the total knowledge score. As bowel cancer knowledge score was significantly related to perceived self-efficacy, perceived susceptibility and having participated in screening in the past in bivariate analyses, all of these variables could not be included in the same logistic regression model. Thus, two logistic regressions were performed – one excluding these three variables and another including them, but excluding the knowledge variable. Marital status was almost significantly related to knowledge (p=0.054) and initially retained in both models, however was subsequently removed from model 1 as it caused unstable odds ratios and wide confidence intervals. Thus, the first model included 12 of the 26 variables and the second included 10. A backward step-wise approach using the default ‘enter’ method in SPSS was utilised, removing variables from the model that were non-significant until only variables with a p <0.05 remained in the model.
A total of 93 participants were recruited for this study (Table (Table2).2). Females were over-represented with less than 25% of respondents being male. The majority (47.8%) were in the 45-54 year age group, around half (52.7%) were married or living in de-facto relationships, 44% had either completed senior high school or a post-school qualification, and over half (56.7%) were unemployed or not working. Most respondents were enrolled with Medicare but only 17% had private health insurance. English was the primary language spoken at home for most (92.4%), with 28% rating their English reading ability as poor-fair.
Over 80% had a regular GP and had seen a doctor within the past 12 months (Table (Table2).2). Half (50%) reported having participated in any cancer screening in the past 2 years, and 15% had undergone a colonoscopy. Only 5.6% (5/90) of respondents reported ever having done a FOBT/bowel screening test.
The majority (78%; 72/92) of respondents reported having heard of bowel cancer, although of those, only 15% (11/72) could give a correct description of any aspect of bowel cancer (for example, ‘cancer of the bowel or digestive system’). Less than a third were aware of what polyps were (29%, 25/86) and only 19 of the 25 (76%) who said they knew what a polyp was, were able to describe it correctly. A small proportion (14%, 13/90) of respondents reported knowing what an FOBT/bowel cancer screening test was, and even after being given a detailed explanation and description of the FOBT screening test,1 only 30% (27/91) said that they had heard of this test (data not shown).
Those who had heard of bowel cancer before were 6.6 times more likely (X2=7.1, p=0.008) to have seen or heard media advertising related to bowel cancer screening, and those who had heard of the FOBT/screening test were 13 times more likely (OR=13.5, p<0.0001) to have been exposed to such media advertising (data not shown).
Responses to individual knowledge items including identification of risk factors and signs and symptoms are detailed in Table Table3.3. The risk factor identified least frequently was having a close relative with bowel cancer, with only 56% (52/93) of respondents recognizing this as a risk, whereas 70% (65/93) were aware of excessive alcohol consumption as a risk factor. Most (87%, 81/93) recognized bleeding from the bowel as a symptom of bowel cancer, whilst more vague symptoms were less likely to be identified. Importantly, only 57% (52/92) were aware that bowel cancer could be asymptomatic.
Composite knowledge scores ranged from 0-18 and the mean knowledge score was 13.3 (median=15, SD=4.3, n=93). Knowledge was not related to demographic variables such as age, education or income. Significant relationships existed between knowledge and having participated in screening in the past or having undergone a colonoscopy, frequency of doctor visits, and family experience of cancer. Exposure to media advertising bordered on having a significant association with knowledge of bowel cancer (p=0.051). In addition, knowledge was also related to perceived self-efficacy and perceived susceptibility (see Table Table44).
Perceived susceptibility to bowel cancer was low in our sample with only one-third (32%, 29/91) believing they might be at risk, and only 14% (13/92) reporting that their chance of getting bowel cancer was either high or very high (Table (Table5).5). Perceptions of severity indicated that over three quarters (77%, 69/90) felt it was a serious disease agreeing with the statements, ‘If you had bowel cancer your whole life would change’. Despite this, most (82%, 75/92) believed ‘bowel cancer can be cured if found early’. Fatalistic attitudes prevailed among a large proportion of respondents who agreed that getting bowel cancer was a death sentence (42%, 39/92 ) and that nothing can be done to prevent getting the disease (35%, 32/91). One quarter (24%, 22/91) also reported feelings of shame associated with a bowel cancer diagnosis. Only about half (53%, 49/92) rated their confidence (perceived self-efficacy) to carry out the FOBT as confident or very confident.
Generally, respondents agreed with most statements of benefits associated with FOBT screening (data not shown). The items respondents most frequently agreed with in terms of barriers to screening were being afraid to find out something is wrong (44%, 41/93) or finding out they have cancer (39%, 35/91) and not understanding how to do the test (36%, 34/93). Not having symptoms (31%, 29/91) or privacy to do the test (26%, 24/91) were also reported as constraints by about a quarter of respondents. Not having an appropriate place to store stool samples was an issue for substantial numbers of participants (40%, 37/93), as was feeling well and not having symptoms (31%, 28/93), having to mail the kit back (29%, 27/93) and not having a family history of bowel cancer (26%, 24/93).
Overall, 63% (58/92) of respondents reported they would consider doing the FOBT screening test in the next 6-12 months if they received it (Table (Table6).6). Interestingly, a larger proportion said they would do the test if their doctor recommended it (84%; 77/92). Those intending to complete an FOBT test were significantly more likely to do a test if a doctor recommended it, while those who said they would not consider doing a test were more likely not to do a test even if a doctor recommended it (X2, n=92)=30.6, p<0.0001), suggesting that those refusing to consider FOBT screening remained unlikely to do so despite a doctor’s recommendation (data not shown).
Table Table66 summarises the relationship between intention to screen with FOBT and a number of socio-demographic, knowledge and attitudinal variables.
Those who intended to participate in screening were more likely to be married or in de-facto relationships (OR=5.96, 95% CI=2.3-15.7), employed, (OR=3.14, 95% CI=1.2-8.6) have a higher income (OR=2.8, 95% CI=0.99-7.8), at least 8 years of education (OR=2.6, 95% CI=1.0-6.8), and have seen a doctor within the past year (OR=5.4, 95% CI=0.98-29.6). Participation in other types of cancer screening (OR=3.8, 95% CI=1.5-9.6) and knowing a family member with cancer (OR=2.7, 95% CI=1.1-9.9) also increased the likelihood of screening uptake. Those who had previously had a colonoscopy were nine times more likely (OR=9.2, 95% CI=1.2-74.3) to consider screening.
A direct association was observed between bowel cancer knowledge and intention to screen, with the proportion intending to screen increasing as knowledge score increased. Compared to those with a low knowledge score, respondents with medium knowledge were 8.5 times (p<0.0001) more likely to consider screening and those with high knowledge score were nearly 10 times (p<0.0001) more likely to consider screening. Those who were aware bowel cancer can be asymptomatic, and that bowel cancer can be cured if found early, were also significantly more likely to consider screening.
One of the most significant associations with screening intention was perceived self-efficacy or confidence in carrying out the self-screening test. Those who felt confident or very confident were over 13 times more likely to screen (OR=13.4, 95% CI=4.6-38.6). A greater perceived risk was also related with intent to screen (OR=2.96, 95% CI=1.1-8.3), as was perceived severity but only for one of three items (Do you think bowel cancer can be cured if found early? OR=4.15, 95% CI=1.4-12.6). No significant association was observed between having a fatalistic attitude or greater awareness of benefits of screening. Those who did not perceive a bowel cancer diagnosis to be shameful were five times more likely to consider taking up screening (OR=5.05, 95% CI=1.7-14.7).
The first multivariate logistic regression model which excluded bowel cancer knowledge score, identified being aged 45 or more, having greater perceived self-efficacy, and having participated in screening in the past as independent predictors of intention to screen with FOBT. In the second model, bowel cancer knowledge score and marital status remained significant independent predictors of screening intent (Table (Table77).
This is the first published study to examine awareness, knowledge, attitudes and behavioural intention in regard to bowel cancer screening in the Indigenous Australian population. Given significantly lower levels of CRC screening participation by this population group, it is critical to elucidate reasons behind lower uptake to ensure good evidence informs program policy makers in the design of ongoing and future health interventions.
This study indicates that among the population we sampled, general awareness of CRC and CRC screening was low. Most had heard about bowel cancer but were not able describe any particular detail of what it was or what polyps were, and the vast majority had not heard of bowel cancer screening or the FOBT test. The evaluation of Australia’s NBCS pilot program also showed that inadequate understanding and awareness of bowel cancer were major impediments to the participation of Aboriginal people in bowel cancer screening .
Having seen media advertising on bowel cancer screening was significantly associated with greater awareness and higher overall bowel cancer knowledge scores, consistent with findings reported by Schroy et al. examining the effect of media on awareness . Despite this, media exposure was not an independent predictor of screening intention among our respondents, suggesting that although it has a critical role to play, it is insufficient on its own. Exposure to media promotions prior to receiving a screening kit was found to be an important trigger for participation for Indigenous people in the final evaluation of the NBCSP pilot program in 2002. This suggests a pivotal role of mass media for public education and raising the profile of bowel cancer  and confirms the recommendations of its use to raise awareness and ultimately facilitate screening participation in minority groups .
Knowledge of specific bowel cancer risk factors was reasonable, with about two thirds or more of participants identifying the main risk factors. However, that over half of participants did not know bowel cancer can be asymptomatic, suggests this is an important concept to be emphasised in education and awareness campaigns.
Factors significantly associated with bowel cancer knowledge included having participated in cancer screening in the past, seeing a doctor more often, having a family or personal experience with cancer, having been exposed to media advertising about bowel cancer screening, greater levels of perceived self-efficacy and perceived susceptibility. Most of these factors are related to exposure to experiences that facilitate greater cancer awareness and knowledge, implying that knowledge can be gained and is not necessarily determined by education, income or age.
Perceived susceptibility to CRC was generally quite low, with only a third of our sample believing they were at risk despite the majority being aged over 45 years, and is in line with findings elsewhere in the literature . Greater perceived risk to a disease can in some cases be associated with more positive preventive behaviour  and our study also showed that those with a greater perceived risk were significantly more likely to consider FOBT participation. However, perceived risk was not an independent predictor of screening intention, supporting the theory that despite being important in influencing CRC screening behaviour, it requires other mediating factors to have an effect .
Intention to screen for bowel cancer was relatively high among our respondents with almost two-thirds reporting they would undertake FOBT screening in the future if they received a kit. This is much higher than the 17% participation rate observed from the most recent report of Australia’s NBCSP , but equivalent to that found in a study of rural Australians and low-income, ethnically diverse groups in the US [31,40]. An even greater proportion of respondents said they would do the FOBT test if their doctor recommended it - a response which supports research that shows endorsement of screening by a primary care practitioner can facilitate participation [32,41,42]. These results suggest that doctors and possibly other trusted health providers have an important role to play in encouraging screening adherence. It also supports findings from the NBCSP evaluation which demonstrated that Indigenous people needed extra support and encouragement to participate in CRC screening .
Bivariate analyses indicated that intention to take up FOBT screening was significantly higher among those who were married or in de-facto relationships, employed, had at least eight years of education, higher income, and a history of undergoing cancer screening or a colonoscopy. Existing research also shows that lower CRC screening uptake is consistently observed among those who are less educated and from lower income groups, and those from non-English speaking backgrounds [20,43-45]. In contrast with the literature, English reading ability was not related to screening intention in our study , however, this measure was self-reported. Moreover, respondents with greater overall knowledge and awareness of bowel cancer and the screening test, greater perceived self-efficacy and perceived susceptibility to the disease were also more likely to consider screening, as were those who personally knew someone with cancer.
On multivariate analysis, significant predictors of screening intention were, being aged 45 years or more, having greater levels of perceived self-efficacy or confidence in carrying out the FOBT, and past participation in cancer screening. Past screening participation was also demonstrated to be an independent correlate of CRC screening uptake in several studies [29,47], and although our research does not directly measure participation, intention to participate can provide some indication of behaviour.
One of the strongest associations and independent predictors of screening intention in our sample was perceived self-efficacy. This is highly pertinent to the Australian program as bowel cancer screening is entirely based upon a self-screening kit delivered by post, which in urban areas is to participant’s homes, although mail is not delivered to homes in some rural and remote areas. Self-efficacy has not been explored extensively in the literature as countries such as the US and UK promote alternative methods for CRC screening such as colonoscopy or sigmoidoscopy alongside FOBT. Feufel et al  have shown that improved instructions accompanying self-screening FOBT tests can help facilitate appropriate of test completion. This is particularly relevant for Indigenous Australians who had a higher proportion of incorrectly completed FOBT tests compared to the general population .
In the second logistic regression model, bowel cancer knowledge and marital status remained independent predictors of intention to screen. Knowledge and awareness can be important determinants of screening behaviour, as a greater understanding of a disease, its risk factors and methods of prevention affects an individual’s decision to participate in screening. Lower knowledge levels are associated with a lower perceived risk and poorer CRC screening adherence rates in studies with ethnic minorities . An Australian study also found that those born overseas had poorer bowel cancer knowledge scores compared to those born in Australia, with knowledge a predictor of screening intent . Our research finds a strong relationship between bowel cancer knowledge score and intention to screen for CRC, with screening intention increasing with each increase in knowledge tertile. This relationship was retained in multivariable analyses and is line with other research demonstrating knowledge to be a significant predictor of bowel cancer screening uptake [29,47,49]. Enhancing knowledge can also lead to more positive attitudes towards the disease and reduce negative perceptions, which could in turn impact positively on screening uptake . Health education and promotion should therefore focus on improving overall knowledge related to bowel cancer and screening as a means to facilitate screening compliance.
Previous studies have reported associations between screening intent and fatalistic attitude towards bowel cancer [50,51], but this was not evident in our study despite the large proportion of respondents possessing a fatalistic attitude. Shame was strongly associated with intention to screen in bivariate analyses but was not an independent predictor of screening intent. Concerns about shame and embarrassment differed from those observed in studies of Latinos , yet corroborated findings from other ethnic minority groups [52-54]. This shows the need for culturally targeted education and screening promotion campaigns to address the differing beliefs and views towards bowel cancer screening that exist between different cultural groups in order to deliver appropriate messages that are effective.
Most participants agreed with the benefits of CRC screening, although this did not appear to influence screening intent among our sample, and is unlikely to be a successful focal point in prevention or education campaigns. Similar findings have been observed in a study of African Americans . Why this is the case needs to be explored in greater depth, but it may be related to not understanding personal risk or that perceived barriers have a larger impact on screening decisions.
Fear of finding out something is wrong or finding out they had cancer were major barriers to FOBT screening for over a third of our sample. This is similar to research undertaken with Italian migrants in Australia that found fear of cancer and finding out they have cancer were major barriers to screening . In the present study, additional barriers related to the design of the screening program and test method including the postal distribution, storage of samples, and lack of privacy in which to do the test. The absence of symptoms and not having a family history of bowel cancer were also reasons that respondents felt discouraged them from screening. Again, the concept of self-efficacy arose with ‘not knowing what to do’ being reported by over a third of respondents as a major reason they would not complete the screening test. These barriers cannot be ignored and most are heavily impacted by the way the screening program is designed and delivered to the Australian population. Research into test preferences for Indigenous people is an area that is under-investigated and is warranted if screening rates for bowel cancer are to be increased [55,56].
Several limitations to this study must be noted. As our sampling strategy was non-random, the results of this study cannot be considered representative of all Indigenous Australians. Participants were recruited primarily through respected community members working in health settings and are therefore likely to be more health connected, proactive in their health behaviour, better informed about health issues and have greater exposure to prevention messages. Furthermore, participants lived in urban and regional centres so results may not reflect the views of those living in very remote regions and living traditional/nomadic lifestyles.
The over-representation of females limited our ability to find differences in knowledge or intention to screen across gender. The nature of gender relations in Aboriginal culture may have influenced our ability to recruit male participants as well as the fact that all researchers involved in data collection and recruitment were female. The higher proportion of females and persons unemployed or not working in this study occurred because these groups are more likely to have the time to take part.
Our main outcome measure was largely hypothetical, asking participants on their future ‘intention’ to take up CRC screening. Such questions may not translate or predict real life behaviours, so results need to be interpreted with caution. Nevertheless, considering undertaking a preventive behaviour is a first step towards behaviour modification and therefore remains important.
Additionally, knowledge items from the survey were based on recognition rather than recall, limiting how far this information can be extrapolated. We felt that this approach would elicit greater responses than recall on its own, and it is more commonly used in studies with ethnic and minority groups [32,33].
Finally, our small sample size was a major limitation on the extent of analysis that could be conducted, and is partially responsible for the wide confidence intervals observed particularly in the multivariate analysis. Despite these limitations, our results have generated important information on Aboriginal views of bowel cancer and bowel cancer screening in an otherwise unexplored area of Indigenous health.
Critical to developing interventions for addressing the underutilisation of CRC screening among Indigenous Australians is an understanding of the factors that influence or determine screening adherence. Our study identifies key areas of focus for future health promotion and education strategies and provides policy makers an insight into specific areas that need to be addressed in regard to the way the program is currently being delivered.
Less than six percent of our sample reported having completed an FOBT test which is surprising given that the majority were in the age group targeted by the NBCSP, and is substantially lower than what has been reported from the NBCSP and lower than Indigenous participation in other countries . This may be a reflection of the inappropriate design of the program which is not reaching those high risk age groups it is designed to . All respondents reported being enrolled with Medicare and should have successfully received a screening kit if address details were up to date. A large proportion of our sample were between 45-54 years of age and according to a Cancer Council report , screening kits were being targeted to Aboriginal people from the age of 45 years. It is also possible that the short time since the NBCSP had operated in WA (beginning in 2007) and the recall of kits in late 2009 may have contributed to the low rate reported for having received a kit.
The design of national screening programs often do not take into account the social and cultural diversity of the population in which they are implemented. A recent analysis of Australia’s NBCSP described several inequities in access to screening for Indigenous and minority groups in relation to the way the program is designed and disseminated to the public . The postal distribution of the FOBT and requirement for individuals to self-screen, means the decision to carry out the test at home is made without health provider consultation. Our study also showed that these are significant barriers to screening participation. Inadequate consideration is given to low literacy populations, and the finding that self-efficacy is a major determinant of intention to screen lends further support to this.
Our study also illustrates the importance of improving individual’s knowledge on bowel cancer and confidence to carry out the FOBT test as a means to facilitate CRC screening uptake with FOBT among Indigenous communities. Health education strategies need to focus on demonstrating how the test is done to increase potential participants’ confidence levels, as well as informing community members of the risk factors and signs and symptoms, emphasising the absence of symptoms that can occur with CRC. Our study also supports the role of the media in raising awareness and knowledge on bowel cancer screening and its potential as a mediator of screening uptake. Greater media promotion can assist in eliminating stigma and shame associated with talking about an issue that may be a source of embarrassment and sensitivity for many. The attention that comes with having a celebrity or well respected community member speak about cancer can also be beneficial and encourage screening uptake [57,58].
Future studies should focus on targeting a larger cohort of Aboriginal people including those living in remote and very remote regions whose views can differ significantly from urban and regional populations. The NBCSP was implemented in WA only two years prior to this study, which meant that few participants had actually received an FOBT test kit making detailed exploration of reasons for uptake or non-screening difficult. Future research when the population is more familiar with the screening program may provide greater clarity of reasons impeding or facilitating uptake of screening.
1 Explanation of FOBT given to respondents: ‘An FOBT is a screening test for bowel cancer that is carried out on healthy people with no symptoms. This test can pick up tiny amounts of blood in a sample of your bowel motion that you yourself may not notice. Blood in the stools is one sign of bowel cancer. This test is posted to you in the mail so that you can do it at home by yourself by taking a small sample of two bowel motions using sticks provided in a kit. You then return this kit by mail to be tested. After it is tested you and your GP are notified by mail of your result. If your test is positive for blood then it will need further investigation and you will be referred to have a colonoscopy at the nearest hospital.’
The authors declare they have no competing interests.
AC coordinated the study, participated in the study design, carried out the data collection and analysis, and drafted the manuscript. SCT was involved in the initial conception of the work, assisted in the conduct of the study, sourcing funding and in refinement and editing of the manuscript. Both authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
This work was supported by the Western Australian Cancer and Palliative Care Network, Department of Health, Western Australia.
The authors thank Pauline Gregory, Susan Hurst, Trudi Cornish and Gail Mongoo for assisting with participant recruitment and data collection. We also gratefully acknowledge Jenny Lalor, Dr Judy Katzenellenbogen and Dr Victoria Briones Chiongbian for their assistance and advice with data preparation and analysis, and Kath O’Connor and Gloria Sutherland for their support for this project. Our thanks also go to all participants and Indigenous health services that agreed to be part of this research.