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Non-participation in population-based disease prevention programs in general practice
© Koopmans et al.; licensee BioMed Central Ltd. 2012
Received: 27 April 2012
Accepted: 21 September 2012
Published: 9 October 2012
The number of people with a chronic disease will strongly increase in the next decades. Therefore, prevention of disease becomes increasingly important. The aim of this systematic review was to identify factors that negatively influence participation in population-based disease prevention programs in General Practice and to establish whether the program type is related to non-participation levels.
We conducted a systematic review in Pubmed, EMBASE, CINAHL and PsycINFO, covering 2000 through July 6th 2012, to identify publications including information about characteristics of non-participants or reasons for non-participation in population-based disease prevention programs in General Practice.
A total of 24 original studies met our criteria, seven of which focused on vaccination, eleven on screening aimed at early detection of disease, and six on screening aimed at identifying high risk of a disease, targeting a variety of diseases and conditions. Lack of personal relevance of the program, younger age, higher social deprivation and former non-participation were related to actual non-participation. No differences were found in non-participation levels or factors related to non-participation between the three program types. The large variation in non-participation levels within the program types may be partly due to differences in recruitment strategies, with more active, personalized strategies resulting in higher participation levels compared to an invitation letter.
There is still much to be gained by tailoring strategies to improve participation in those who are less likely to do so, namely younger individuals, those living in a deprived area and former non-participants. Participation may increase by applying more active recruitment strategies.
The number of people with a chronic disease will strongly increase in the next decades. For example, the worldwide prevalence of diabetes mellitus, is expected to increase by 54% from 2010 to 2030 . Chronic diseases are responsible for a considerable burden to both the individual and to the healthcare system. Consequently, it is expected that the demand on health care will rise excessively, and preservation of good quality healthcare becomes unaffordable.
In order to reduce the disease burden for people and to keep healthcare affordable, a shift from treatment of an individual with a disease towards maintenance of health or postponement of disease, becomes inevitable.
General Practitioners (GPs) play an important role in prevention, since they deliver comprehensive, holistic and easily accessible care. GPs generally provide preventive care in the individual setting of a consultation, either on the indication of present risk factors and symptoms of disease or care-related, for example to reduce the risk of complications of chronic disease. Population-based prevention has a less prominent role in General Practice . Population-based prevention programs initiated by GPs potentially contribute significantly to reduce the risk of developing chronic diseases or to identify treatable diseases at an early stage (disease prevention).
Current examples of population-based disease prevention programs embedded in General Practice include vaccination programs (e.g. vaccination for influenza) and screening programs (e.g. screening for cervical cancer). The purpose of vaccination is to prevent infectious diseases or to diminish the impact of infectious diseases. Population-based screening aims at early detection of a disease, thereby increasing the chance of successful treatment and diminishing the impact of the disease, or it intends to identify persons with a high risk of developing a chronic condition, whereby changes in lifestyle and/or use of medication could reduce this risk substantially. Prevention programs embedded in General Practice practices are usually applied in individuals with a potential elevated risk of disease, since this is thought to be the most (cost) effective approach ; only those who might benefit most are invited, whereas the number of those who undergo clinical measurements is minimized. Furthermore, in this manner workload in General Practice is limited.
The potential gains of prevention in persons with an elevated risk of disease are considerable, yet the challenges in changing health risks are numerous. Health benefits of the total population increase by increasing participation levels of high risk individuals. However, participation levels are often suboptimal and differ between groups. To increase this level, it is important to know which individuals are less likely to participate and to understand their reasons and barriers. Previous studies showed that numerous socio-demographic and behavioural factors may play a role, as well as factors on a community or organizational level [4–8]. In addition, factors, such as the nature of the target condition  and the program itself , may also play a role in the willingness to participate. Finally, the method of recruitment might influence the participation level as well .
The aim of this systematic review is to identify factors that negatively influence participation in population-based disease prevention programs in General Practice and to establish whether the program type is related to participation levels.
Data sources and searches
A systematic literature search was conducted in Pubmed, EMBASE, CINAHL and PsycINFO to identify relevant articles published between January 1st, 2000 and July 6th, 2012. Language was restricted to English and Dutch. The search strategy was formulated in Pubmed and adapted to the other databases (see Additional file1: Appendix 1 for the search strategy). When necessary, equivalents for the MeSH terms were used or MeSH terms were used as free text words.
The first two stages of the selection for inclusion; in succession, the screening of titles, and abstracts, were performed by the first author (BK). JK also screened a random 10% of the abstracts and interrater agreement was high (kappa 0.89). All articles were screened on full text by two authors according to the criteria presented in Additional file 2: Box 1.
We aimed to select articles including information on non-participation in population-based disease prevention programs aimed at high-risk individuals in General Practice. This type of programs include an active approach of inviting a pre-defined target group to undergo screening or vaccination.
Programs had to be population based, and therefore not related to the individual care setting (e.g. opportunistic screening following complaints of the patient), and
aimed at high risk individuals.
Programs needed to be performed in General Practice.
Studies needed to give information on either characteristics or reasons of non-participation or both.
Furthermore, to be included, articles had to describe original studies.
BK screened all articles, JK and MN screened each half of the articles. Disagreements were solved by the authors who screened the article, in case of no consensus, the third reviewer was consulted and the majority decided.
general information: first author, year of publication, design, sample size and country where the study was conducted.
general information of the program: target disease, inclusion criteria of the target group, recruitment strategy, sending of reminders, variables used to compare participants and non-participants.
information on participation levels and willingness to participate.
For reasons of efficiency, only the significant differences between non-participants and participants were mentioned in the results section. In addition, results were presented in a narrative summary of characteristics that negatively influence participation, rather than in terms of effect sizes.
Studies were grouped based on the goal of the program (program type): 1) vaccination, 2) early detection of disease and 3) identification of high risk of a disease. Furthermore, to avoid duplicate presentation of the same data we grouped studies within the same population. Non-participation levels, significant characteristics of non-participants and their reasons when mentioned in both studies were only presented once, using the results of the study including the largest sample size within the same population.
Assessment of study quality
Existing quality assessment instruments mainly focus on the quality around the primary outcome, rather than to secondary issues as is the case in our review. Therefore, we assessed quality of the studies based on the presence (or absence) of our main inclusion criterion. Studies not including characteristics or reasons of non-participants were found of insufficient quality and therefore excluded. Studies including characteristics or reasons of non-participants were found of moderate quality and received one asterisk, studies including both characteristics AND reasons of non-participants were found of higher quality and received two asterisks.
Two of these articles [10, 11] were excluded because of double publication of part of the results of the same large study, which were presented all together in one other article , leaving 28 articles for inclusion. Two of the included articles [13, 14] were conducted in the same study population but with other study aims, and three studies [15–17] were performed in a subpopulation of a large study [18–20]. Therefore, this review includes studies in 24 original populations. Reasons to exclude articles after screening of the full text were lack of information about non-participation (58%), prevention program was not initiated by GPs or no separate data of the General Practice setting was presented (17%), or because the program was not a population-based prevention program (13%).
Characteristics and non-participation levels of included studies
First author and year
Study size (n)
Inclusion criteria target group
Allsup , 2002
Age (65–74), medical record
Letter + reminder
Arthur , 2002
Age (≥ 75)
health check + vaccination: 26% vaccination in clinic: 32%
Evans , 2003
Age (≥ 65)
Age (≥ 75)
1997: 52% 1998: 50% 1999: 49% 2000: 37%
Byrnes , 2006
Age (≥ 65)
Telephone + reminder
2004: 23% 2005: 17%
Opstelten , 2009
Herpes zoster and influenza
Age (≥ 65)
Letter + reminder
HZ (with and without influenza): 61%, Influenza (with and without HZ): 24%
Vila-Córcoles , 2006
Pneumococcal bacteraemia/invasive disease
Age (≥ 65)
2001: 56% 2002: 49% 2003: 48%
Screening aimed at early detection of disease
Moser , 2009
Age (25–64), female sex
Tacken , 2007
Age (30–60), female sex
Letter + reminder
Low , 2005
Letter + reminder
Verhoeven , 2004
Age (18–35), female sex
In General Practice practice
Age (40–69), medical record
Observational study Controlled trial
Age (40–69), medical record
Letter + reminder
Age (40–69), medical record
Marteau , 2010
Age (40–69), medical record
Van der Veen , 2009
Depression and anxiety
Age (18–65), recent contact PCP, medical record
Yeung , 2006
Age (≥ 18), ethnicity
In General Practice practice
Fowler , 2012
Age (≥ 65), medical record
In General Practice practice
Screening aimed at identification of high risk of disease
Vermunt , 2010
Age (40–70), medical record
Van de Kerkhof , 2010
Age (40–75), medical record
Nielen , 2011
Age (45–70), medical record
Letter or poster and leaflets in waiting room
Letter: 67% Poster/leaflet: 99%
Lambert , 2011
Age (≥ 40), male sex, medical record
Letter or telephone call
Barr , 2005
Age (≥ 70), female sex
Zanjani , 2006
Age (≥ 65)
Study quality is presented in Table 1. Twenty original studies were qualified as ‘moderate’ [9, 13–20, 22–34, 37, 38]. Of these studies, one assessed reasons of non-participation . Four studies were of ‘higher’ quality [12, 21, 35, 36]. No differences were found in levels of non-participation between studies of moderate and higher quality.
Recruitment of the target group was performed by sending a letter on behalf of the GP in 17 studies (71%), in three studies individuals of the target group were invited in the practice prior to their consultation, regardless their complaints [29, 31]. In one study the target group was partly invited by telephone  and in another study by using posters and leaflets in the waiting room . In six studies participation levels were compared using different recruitment strategies, namely an informed choice versus a standard letter, vaccination at the clinic versus a health check plus vaccination at home, an invitation letter versus posters and leaflets in the waiting room, using telephone recruitment and booking, and loss framed versus gain framed messages (information on screening aimed at what people may lose by not participating versus what they may gain by participating) [9, 14, 22, 23, 34, 35].
Non-participation in population-based disease prevention programs
In general, non-participation levels showed a very broad range from 10% to 99% (median 38%) (see Table 1). Not only between studies targeting different diseases, but also within studies targeting the same disease, differences in non-participation levels were high.
Summary of significant socio-demographics and behavioural factors related to non-participation
Factor (n studies used) #
N studies stat. sig. (%)
Non-participation early detection of disease
Non-participation identification high risk of a disease
Stronger belief that physician wants women to attend screening  Less strong feeling a personal moral obligation  Higher treatment control  Lower negative emotional perceptions  Lower perceived benefit 
Less evidence was found for socio-demographic factors to play a role in non-participation. Age, sex and socioeconomic status (SES) were significantly related to non-participation in respectively 75%, 53% and 50% of the studies, but the effects of these factors remained unclear since results contradicted. However, non-participants are likely to be younger (in 11 out of 15 studies) [9, 19, 20, 30, 33, 36–38] and male (in 6 out of 9 studies) [12, 19, 20, 30, 33, 36]. Furthermore, there was some indication that non-participants were more likely to be living in deprived area’s [9, 12, 18, 20] and to have a lower health consumption [9, 13, 20, 33] (data not shown).
Health status, which was operationalized in various ways (e.g. presence of unhealthy lifestyle factors or chronic disease and self-reported health) was in both positively and negatively related to participation in an equal way. Only a few studies included physical environment and practice related factors and the effect of these factors therefore remains unclear.
More detailed information per study of factors included and factors significantly related to non-participation is presented in Additional file 3: Appendix 2.
Related to recruitment strategy, non-participation levels within comparable programs were lower in studies in which a more active recruitment strategy was used to improve uptake, including vaccination at home , telephone recruitment and booking , and recruitment in the practice compared to studies in which a personal invitation by letter was used [29, 31]. Also, offering a paper  instead of an on-line risk questionnaire  resulted in higher uptake in comparable programs.
Furthermore, a more passive recruitment strategy (posters and leaflets in the waiting room) resulted in a much higher non-participation level compared to an invitation letter in the same study .
No clear difference could be found between the program types with respect to non-participation levels. They all showed a similar very broad range in non-participation levels (vaccination: 17% to 88% (median 32%), early detection: 10% to 65% (median 27%), and identification of high risk: 25% to 99% (median 52%)) (see Table 1). Furthermore, no indication was found of differences between the three program types with respect to factors related to non-participation.
To our knowledge, this is the first review on non-participation in vaccination programs as well as population-based screening programs embedded in General Practice.
In total, 28 studies in 24 original populations matched our search criteria regarding three program types: vaccination, early detection of disease, and identification of high risk of a disease. Non-participation levels ranged between 10% and 99% in all three program types. Median non-participation level was 38%. This review showed that program type does not seem to influence non-participation in population-based disease prevention programs in General Practice. In addition, no differences were found between the three program types with respect to factors related to non-participation. However, within each program type, and even within programs targeting the same disease, considerable differences were shown, which may be partly related to differences in recruitment strategies used.
Three groups were identified which might need specific attention, since they are less likely to participate in population-based disease prevention programs in General Practice; younger individuals, the people living in a socially deprived area, and former non-participants. In general, non-participants found participation not to be of personal relevance.
A previous review on vaccination programs also showed younger individuals to be less likely to participate, however, screening studies showed ambiguous outcomes of age [6, 7]. Living in socially deprived area was also shown to be related to non-participation in vaccination programs  as well as in colorectal and cervical cancer screening [39, 40]. Previous non-participation, either in the same or other programs is a strong predictor of current non-participation , which was also reflected in the lower likelihood of non-participation in individuals with a higher health care consumption in the diabetes screening programs [13, 20]. An explanation could be that people get familiar with the tests and procedures involved and overcome their barriers.
Lack of personal relevance and low perceived risk are important factors in non-participation [7, 41, 42]. People may not respond since they feel and think they live healthy . However, risk of disease is also a difficult concept for people to understand and often underestimated, especially in diseases that may be preventable by behavioural change .
The lowest non-participation levels were seen in programs applying more active and personal approaches, including recruitment in General Practice. A passive approach including recruitment by posters and leaflets in the waiting room of the General Practice practice, resulted in only little participation . Personal contact with a GP or nurse therefore seems to play a decisive role in increasing participation . Two other reviews showed that invitation, reminding, and counselling by telephone all seem to be effective interventions to increase uptake, however, they are much more intensive and expensive [6, 44]. Furthermore, the results of this review indicate that it might be important to more specifically address to the personal relevance of vaccination and screening. Recent studies showed that the concept of risk is better understood if information is presented in terms of natural frequencies rather than as an absolute or relative risk . In addition, low future time orientation, as often seen in the socially deprived, may be addressed to, since this is associated with a lower likeliness of changing (health) behaviour. Invitations should therefore stress the immediate benefits and remove barriers to e.g. participate in vaccination or screening and/or changing lifestyle [8, 46].
Noticeably, relatively few programs were aimed at identification of high risk of disease. For example, only one out of eight of programs focused on diabetes was aimed at identifying high risk of this disease. The relatively low participation level in this study may have been due to the fact that the invitation letter informed individuals that when they were at high risk of diabetes they would be offered a lifestyle intervention. The prospect of having to change ones lifestyle may have discouraged some people to participate .
Our inclusion criteria are mainly related to health care systems in which the GP is a gatekeeper, which is the case in the Netherlands. Within this system GPs are able to pro-actively invite potentially high risk individuals within their patient population. This is reflected in the studies presented in this review. In countries with a non-gatekeeper system, the described programs would be performed in an opportunistic manner, which was an exclusion criteria in this review. Furthermore, population-based prevention programs in Europe are generally free of charge, while individuals in the USA have to pay or get reimbursement through their insurance. Generalizability of the results of this review, therefore, may be limited.
Some limitations of this systematic review can be noted. First, as with systematic reviews in general, despite of a thorough search strategy, relevant (un)published studies may have been omitted, as well as non-English or Dutch articles. Adding the concept ‘feasibility’ to the search strategy may have resulted in more included studies. Additionally, research on breast- and colon cancer screening was not retrieved since these programs need more specific equipment, which is usually not available in General Practice practices. Furthermore, although participation may have been studied, the results may not have been included in the final article. Next, the relatively small number of studies included, and the large heterogeneity in study characteristics and results require cautious interpretation of the results of this review.
Additionally, six included studies were part of the same international trial. Therefore, although we tried carefully to prevent presentation of duplicate data some bias may have been introduced. However, in the UK and Denmark arm of the study different target groups and recruitment strategies were used. In addition, the majority of the included studies were trials instead of real-world programs. This may have led to an overestimation of the participation levels, since these studies may be more likely to be performed in well-organized General Practice practices in less deprived areas. Finally, although we identified some factors that might be related to non-participation, it remains unclear from this review how these factors interrelate.
The findings of our systematic review provide guidance for future research and General Practice. Only 17% of the studies addressed both characteristics and reasons of non-participation. To gain more insight in who is not willing to participate in disease prevention programs and why, it is important to assess both.
Future research on willingness to participate should focus on programs aimed at identifying high risk of disease, since they may have great potential in improving population health but are also more demanding to people than the other two types. Additionally, research should be focused on the consequences this may have for recruitment in these programs.
Recruitment strategies should address to personal relevance, and to be tailored to the specific needs of subgroups of individuals. Those who are less likely to participate, such as individuals living in a deprived area, former non-participants and younger individuals, may need to be more actively recruited, in which contact with a health professional may be pivotal, especially when invited for the first time. For example, GPs and practice nurses may emphasize the importance of participation during regular encounters. In those who are more likely to engage in vaccination and/or screening, an invitation letter signed by the GP may be sufficient.
In conclusion, in this review we did not find clear evidence of program type influencing non-participation in population-based disease prevention programs. In general, conflicting results regarding factors related to non-participation were shown, yet we did find three groups that might be less likely to participate, namely younger individuals, those living in a deprived area and former non-participants. Furthermore, higher participation levels were reached in studies with more active recruitment strategies. Therefore, there is still much to be gained by tailoring strategies to improve participation in those who are less likely to do so.
The authors would like to thank Linda Schoonmade and Rinske van den Berg, clinical librarians at NIVEL for their contributions to the search strategy.
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