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Public knowledge and beliefs about dementia risk reduction: a national survey of Australians
© Smith et al.; licensee BioMed Central Ltd. 2014
Received: 8 February 2014
Accepted: 19 June 2014
Published: 28 June 2014
With the dramatically increasing contribution of Alzheimer’s Disease and other forms of dementia to the global burden of disease, countries are being urged to address this as a public health priority. This study investigated whether Australian adults recognise this as an important health issue, and hold beliefs and knowledge that are consistent with recommendations concerning dementia risk reduction. This research was undertaken to guide national brain health awareness and education strategies.
A cross-sectional telephone survey was undertaken of 1,003 Australians aged 20–75 years. This measured the importance placed on dementia, beliefs and confidence related to risk reduction, knowledge of risk reduction methods, and the perceived age-relevance of these. In analysis the data were stratified by sex, age, educational attainment, household income, language preference and previous exposure to dementia. Multivariable logistic regression was undertaken to identify variables independently associated with beliefs and knowledge.
People aged 60 years and over identified dementia as very important (17.2%) more often than those aged 40–59 years (5.1%) or 20–39 years (2.1%). While 41.5% of respondents believed the risk of dementia could be reduced, 26.9% were very confident that they could achieve this. Mental activity (57.1%) was identified as beneficial much more often than physical activity (31.3%), healthy eating (23.3%) and other cardiovascular health behaviours. Women, people of English-speaking origin, and those having contact with a person with dementia, showed better knowledge of several health behaviours.
Growing attention is being given to population risk reduction to combat the dramatic increase in the burden of disease due to dementia. In Australia many people do not yet hold beliefs and knowledge that support this, which highlights the need for concerted awareness raising that dementia is not an inevitable aspect of ageing, and for education about the role of vascular health in dementia risk reduction.
Alzheimer’s disease and other forms of dementia are among the most rapidly increasing threats to public health globally. In 2012 the Global Burden of Disease Project reported that over the two decades from 1990 until 2010 the total disability adjusted life years due to Alzheimer’s disease and other forms of dementia had risen by 99.3% , an increase of 53.3% per 100,000 persons. Over this period the age standardised death rate due to these conditions was estimated to have risen by 95.4% . Such dramatic rises have been driven by population aging and the epidemiological transition that is underway in many low and middle income countries .
Countries in Western Europe, North America and the developed region of the Western Pacific have been identified as having the highest prevalence of dementia . In Australia, dementia was ranked as the third leading cause of death in 2010 and the fourth highest contributor to the total burden of disease in 2011 . It is projected that the number Australians with some form of dementia will triple by the year 2050 . Similar projections have been made for the United States , the United Kingdom  and nations across Europe .
As a result of the marked increase in the burden of disease due to dementia the World Health Organisation has called for nations to place this issue on their public health agendas. Raising awareness and reducing stigma, improving dementia care and services, and providing support for caregivers are important areas of action . There is also growing support for a proactive approach, to reduce the incidence and delay the onset of dementia through health promotion efforts directed at whole populations [10–12].
Current evidence concerning the aetiology of Alzheimer’s disease and dementia indicates that, apart from age and genetic characteristics, there are potentially modifiable biomedical, behavioural, psychological and social factors associated with disease risk. Biomedical factors that are consistently recognised are diabetes, hypertension, hyperlipidaemia and obesity [13, 14]. Smoking, physical activity, dietary intake and levels of alcohol consumption are behaviours that are related to dementia risk [15, 16]. Psychological and social factors that have been reported to be associated with age-related cognitive decline are depression, cognitive activity and social contact [17, 18]. Recent epidemiological studies which have reported a decline in the prevalence of dementia among the elderly, compared with earlier cohorts, suggest that reductions in risk factors at the population level and improvements in standards of living and health care can lower the burden of disease due to this condition [19, 20].
Determining the relative contribution of the risk factors to different forms of dementia is a research priority and the role of some factors (e.g., alcohol intake), and their interaction with genetic characteristics, is still being explored . Notwithstanding this, the global increases in the Alzheimer’s Disease and dementia, and the observed associations with modifiable factors has prompted researchers and advocates to recommend that population level risk reduction strategies be instigated by government and non-government agencies . A growing number of organisations are heeding this call, demonstrated by initiatives such as the Healthy Brain Initiative in the US , the Your Brain Matters campaign in Australia , the National Memory Programme in Finland  and the Forget Me Not education program in Ireland . This arena of activity has brought with it a need for new evidence, about the prevailing knowledge, beliefs and behaviours concerning dementia and the potential to maintain cognitive health among different population segments .
Studies of public knowledge and beliefs towards Alzheimer’s disease and other forms of dementia have focused predominantly upon perceived severity and personal susceptibility to these diseases, and understanding of symptoms and treatment [28–32]. A review of research about public perceptions of cognitive health in the US found that 3 of 10 studies examined beliefs about lifestyle and brain health, or the potential to reduce the risk of dementia . Of these, the Brain Health Poll undertaken by the American Society on Ageing and Metlife Foundation  was the most extensive, investigating beliefs about whether brain health could be improved and the actions that were believed to beneficial for this purpose. A more recent national survey in Australia  investigated similar questions, with a focus upon dementia risk reduction rather than brain health improvement. Other studies have been undertaken with selected population groups (e.g., older people, carers), used convenience samples, and measured knowledge of a narrower range of risk factors [36–39].
With leading authorities advocating for a public health approach towards dementia there is a need to monitor the extent to which populations have also adopted this perspective. Up-to-date data is required about public knowledge and beliefs, including the importance placed on dementia, the potential for risk reduction, the perceived age-groups for whom this is relevant, the behaviours that should be undertaken, and confidence that these will produce beneficial outcomes. This purpose of the study reported here was to investigate these factors among a cross-section of Australian adults, to determine the prevalence of risk reduction knowledge and beliefs and differences between socio-demographic groups. The longer term objective of this research was to inform the design and targeting of national brain health initiatives.
Study population and sampling
An Australia-wide sample of persons aged 20–75 years was recruited. Participants were required to speak English and not be affected by a mental impairment that reduced their ability to answer the survey questions.
Sampling was undertaken using random digit dialling, by a social research organisation with extensive experience in epidemiological and population studies. Because of the growing number of persons who use a cell phone in preference to a land line, a dual sampling frame was developed that comprised 70% landline numbers and 30% cell phone numbers. In order to improve representativeness, when households were contacted a request was made to speak with the individual who had the next birthday.
Ethical approval for the conduct of the study was given by the Monash University Human Research Ethics Committee (approval no. CF12/2427-2012001309).
Surveys were conducted by trained interviewers over three weeks, from August to September 2012. In order to determine eligibility and complete recruitment, up to six calls were made to establish contact and a further four to achieve completed interviews. The length of surveys was approximately 10 minutes.
To investigate knowledge and beliefs related to dementia, straightforward questions with good face and content validity were used, several of which have been used in previous population studies. In order to measure the personal importance that respondents placed upon dementia as a health issue, the questions used in the US Brain Health Poll  were adopted. These were two open-ended questions which asked respondents to nominate the first and second health issues that it is most important for them to have information about.
Several questions, which had been used in previous surveys commissioned by Alzheimer’s Australia , were asked to determine whether respondents believed that the risk of developing dementia could be reduced, and their knowledge of the behaviours that are beneficial for risk reduction. The first of these measures required individuals to respond, using a 5-point Likert scale, to the question: “Thinking now about dementia, which has many causes including Alzheimer’s disease, please tell me if you personally agree or disagree that it is possible to reduce the risk of a person developing dementia”. Following this an open-ended question was asked: “As far as you are aware, what do you think a person can do to help reduce the risk of developing Alzheimer’s disease or another form of dementia?”. Up to five responses were elicited by means of prompting.
To determine when respondents believed it is beneficial to commence action to reduce dementia, they were asked: “At what age do you think people should start to take action to reduce their risk of Alzheimer’s disease or another form of dementia?” A list of age ranges (<18 years, 18–29 years etc.) were provided to choose from. In order to measure their personal confidence that they can take action to reduce their own risk of dementia respondents were asked: “How would you rate your confidence that you can take action now that will reduce your risk of Alzheimer’s disease or another form of dementia?” A four-point rating scale was given, ranging from very confident, to not confident at all.
The demographic information collected included gender, age, education level, household income and language spoken at home. Respondents were also asked if they had ever had personal contact with a person with dementia.
The sample was weighted to the age and gender distribution of the Australian population. In bivariate analysis, the Chi-squared statistic was used to compare dementia beliefs and knowledge between different strata of respondents. The independent variables in these analyses were: gender; age group (20–39 years, 40–59 years, 60–75 years); educational attainment (up to year 10, high school or technical college, University); yearly household income (less than $40,000, $40,000-$99,000, $100,000 and over); language spoken at home (English, other), and; prior contact with a person with dementia (yes, no). Backwards step-wise logistic regression modelling was undertaken, including those variables where bivariate relationships were observed, to identify those independently associated with dementia beliefs and knowledge. A maximum P-value of 0.1 was adopted to determine retention of variables at each step of modelling. Analyses were carried out using SPSS V19.0.
Characteristics of survey respondents
Mean age (SD)
Completed up to year 10
Completed year 12/TAFE
Full time/Part time work
Up to $39,999
$40,000 to $99,999
$100,000 or more
Contact with dementia
Table 1 shows the unweighted characteristics of respondents in the completed survey, and the profile of the sample after weighting to the sex and age distribution of the Australian population.
Prevalence of knowledge and beliefs about dementia risk reduction
Most important health issues identified by respondents, by age group, with ranking of dementia relative to others
Beliefs about the reduction of dementia risk
Dementia risk reduction
Age groups for action
≤ year 10
Contact with dementia
Knowledge of behaviours that are beneficial for dementia risk reduction
≤ year 10
Contact with dementia
Women more frequently identified mental activity, social activity and a healthy diet as beneficial for dementia risk reduction than men. Respondents aged 60 years and over most often reported that mental activity and social activity are beneficial, whereas the highest proportion who recognised moderate alcohol consumption as beneficial were aged 20–39 years. Those with a university level education most often reported that social activity is beneficial for dementia risk reduction, and those in the highest income bracket most often recognised the value of moderate alcohol consumption. A higher proportion of respondents who spoke English at home recognised the value of mental activity, physical activity and a healthy diet. Respondents with prior contact with a person suffering from dementia also more frequently reported that these three behaviours are beneficial, and that social activity can assist in risk reduction.
Multivariable analysis of factors associated with dementia beliefs and knowledge
Demographic and social factors independently associated with risk reduction beliefs
Dementia rated as important
Believe risk can be reduced
Very confident can lower risk
Believe action should start at <40 yrs
<$40 k (ref)
Demographic and social factors independently associated with knowledge of risk reduction behaviours
≤ year 10 (ref)
Year 11-12/ vocational cert.
<$40 k (ref)
This study has found that many Australians do not recognise dementia as a health priority, and that there is limited understanding of the potential to reduce the risk of this condition through a range of lifestyle behaviours, particularly around mid-life. This indicates that there is great scope to increase awareness that dementia is not an inevitable part of ageing and that, similar to a number of vascular health conditions, the risk of this can be reduced through health promotion action.
Overall, just 7% of respondents rated dementia as one of the top two issues that are important for them to receive information about, which was the same as the proportion of people who nominated “brain health” related conditions as one of their top two issues in the US Brain Health Poll in 2006 . The present study found marked age differences in the perceptions of the importance of dementia, with those aged 60 years and over showing the highest prevalence of concern about this condition. Recent population surveys in other countries, notably France  and Israel , have reported similar findings that worry and fear of Alzheimer’s disease is significantly higher among older respondents.
Of particular concern is that only 5% of those aged 40–59 years rated dementia as very important, even though they are nearing a stage of life when the risk of the condition increases dramatically and studies show mid-life intervention can be beneficial [43, 44]. It may be that this is a reflection of how middle-aged adults rate the severity of, and their personal susceptibility to, dementia relative to other conditions. It was also notable that women were more likely to rate dementia as a priority issue than men. Other researchers have postulated that gender-related patterns such as these may arise from the fact that the prevalence of dementia is higher among women than men . An implication of these findings is that several important population groups may be less likely to attend to information that is disseminated about dementia because of the lower importance they place on this issue .
The potential for the risk of dementia to be reduced is central to the public health message about this condition, and while a substantial proportion of Australians were found to have adopted this understanding, the majority are yet to do so. This differs from previous research in Australia , which found that 72% of Australians believed the risk of dementia could be reduced, and of the US Brain Health Poll, where 53% responded that there is a lot of potential to improve brain health . An explanation for this is likely to be that in the present study only persons who strongly agreed that the risk of dementia could be reduced were classified as having this understanding, in order to identify those who hold views consistent with the information disseminated by government and non- government agencies.
Reporting prior contact with a person with dementia was independently related to a higher likelihood of understanding that the risk of dementia can be reduced. A plausible explanation of this is that this previous contact has lead to exposure to information about the aetiology and risks factors for this condition, which is consistent with studies which have reported that that health literacy is higher among those with greater contact with health services . Unexpectedly, women were less likely than men to strongly agree that the risk of dementia can be reduced, which is inconsistent with evidence that they have a higher level of health literacy than men , and that they more frequently act as primary carers of person with dementia . These gender differences in perceptions about risk reduction may be explained by research concerning the social construction of masculinity and its impact upon health beliefs , which has reported that men are socialised to portray independence and control and to deny vulnerability.
The investigation of confidence to reduce the personal risk of dementia was undertaken to determine the extent to which the public not only understand that risk reduction is possible, but believe that it can be successfully applied to their own lives. There was a substantially lower proportion of respondents with this high level of confidence than there was of respondents who understood that risk could be reduced and, once again, women were less likely to convey this view than men. This confidence reflects the outcome expectancies concerning action to reduce dementia risk which is recognised within social cognitive theory as a determinant of goal development and behaviour [49, 50]. This finding, therefore, shows a low prevalence of a belief that may be a significant mediator between exposure to public health messages about dementia and personal action.
An encouraging finding was that more than half of respondents believed that efforts to reduce dementia risk should commence before 40 years of age. Respondents over 60 years of age were, however, significantly less likely than those age under 40 years to hold this belief, which may be self-affirmation of their own efforts in later life to maintain brain health. The possible reasons for the lower proportion of respondents from high income households who believed that risk reduction should commence in early adulthood are unclear. This may reflect a view among high income persons that they can draw upon clinical services to address the health problems encountered at different stages of life.
While several studies have investigated knowledge of methods to reduce dementia risk, most have used prompted, closed questions [34, 51, 52] which may overestimate knowledge prevalence due to the possibility of correct guessing . The unprompted knowledge question used here found that undertaking mentally stimulating activities was the most widely identified activity that a person could do to reduce dementia risk, which is consistent with the findings of several previous studies [35, 36, 52]. Less than one-third identified physical activity or healthy eating as beneficial, and even lower proportions recognised the role that non-smoking and moderate alcohol intake can play. This shows that there is considerable scope to increase public understanding of the benefits that can be gained for brain health from actions to protect and improve vascular health.
Population segments which showed lower levels of knowledge of several dementia risk reduction behaviours were men, people without prior contact with someone with dementia, and those from a non-English speaking background. There have been few studies which have compared knowledge of dementia risk factors and risk reduction behaviours between ethnic groups. A study in the United Kingdom  did not find differences in risk factor knowledge in a convenience sample of older people from south Indian background and Caucasian backgrounds. In a population survey of dementia literacy in Australia, few differences were found in knowledge of dementia risk factors between persons of Greek, Italian and Chinese backgrounds and those who were third generation Australians. Notably, knowledge of mental activity, physical activity and diet did not differ between ethnic groups. In the present study ethnicity was defined according to language preference, and did not distinguish people according to their cultural background or duration of residence in Australia. The lower levels of knowledge of several risk reduction behaviours (mental activity, diet, alcohol moderation) among non-English speaking persons indicates that public education about dementia needs to be undertaken through culturally specific, as well as mainstream media, and in languages other than English.
This study is one of few population surveys of adults across the age-spectrum investigating beliefs and knowledge concerning dementia risk reduction. In order to achieve a representative sample both landline and cell phone numbers were used in random-digit dialling, and almost 60% of those contacted consented to participate. The profile of respondents was similar to that of the Australian population in terms of age, household income and language spoken at home, however, there was an overrepresentation of people who had attained a university level qualification (40.2% vs 25.4% in Australia, . A further limitation was that, while the survey questions had good face validity, their reliability and validity has not been evaluated.
The growing evidence about the association between dementia and potentially modifiable risk factors, and the significant rise in the global burden of disease due to this condition, has generated wide consensus that a population risk reduction approach must be adopted by policy makers and health promotion agencies. This national survey found, however, that the beliefs and knowledge of adult Australians about dementia are yet to support this perspective. This provides a strong case for dementia risk reduction and brain health to be given greater attention in public health education efforts, and for dementia to be given a higher profile in existing strategies to tackle physical activity, unhealthy eating and other vascular risk behaviors. The data presented here provide a baseline for the measurement of change in public beliefs and knowledge, and identify priority groups for these educational efforts, especially men, people aged less than 60 years, and those from a non-English speaking background.
This work was supported by the Australian Government Chronic Disease Prevention and Service Improvement Fund. The Social Research Centre, Melbourne, conducted the population sampling and telephone surveys for this study. The advice of Glenn Rees, Chief Executive Officer of Alzheimer’s Australia, was helpful for the preparation of this manuscript.
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