Abstract
Compliance with colorectal cancer screening recommendations requires considerable conscious effort on the part of the individual patient, making an individual's decisions about engagement in screening an important contributor to compliance or noncompliance. The objective of this paper was to examine the effectiveness of individual-level behavior theories and their associated constructs in accounting for engagement in colorectal cancer screening behavior. We reviewed the literature examining constructs from formal models of individual-level health behavior as factors associated with compliance with screening for colorectal cancer. All published studies examining one or more constructs from the health belief model, theory of planned behavior, transtheoretical model, or social cognitive theory and their relation to screening behavior or behavioral intentions were included in the analysis. By and large, results of studies supported the theory-based predictions for the influence of constructs on cancer screening behavior. However, the evidence base for many of these relations, especially for models other than the health belief model, is quite limited. Suggestions are made for future research on individual-level determinants of colorectal cancer screening.
Keywords: colorectal cancer screening, decision making, individual adherence, literature review
Colorectal cancer is a serious contributor to disease morbidity and mortality in the United States and other nations. In 2008 it ranked second in cancer deaths and third in new cancer cases in the United States (1); worldwide mortality is over 600,000 deaths per year (2). Screening for colorectal cancer is a cost-effective prevention and control strategy (3); it leads to earlier detection, which is associated with improved survival (4-9). Unfortunately, only about 1/3 of colorectal cancers are diagnosed at an early stage (10-11). This is due to low rates of screening compliance -- only about 1/2 of US adults are compliant with recommendations for colorectal cancer screening (12) and only 15 states have population screening compliance rates greater than 60% (13). Increasing compliance with colorectal cancer screening recommendations is a critical need for reducing the substantial personal and social costs of colorectal cancer morbidity and mortality (14).
Several screening tests are available to detect colorectal cancer and are widely disseminated for use in clinical practice (9, 15-16). There is no single recommended screening test for colorectal cancer, and relative use of each test has changed over time (17). At the time that this literature review was conducted, four screening tests were recommended: fecal occult blood testing (taking fecal samples and placing them on a test card; recommended yearly), flexible sigmoidoscopy (endoscopic procedure that images the lower colon; recommended every five years), colonoscopy (endoscopic procedure with anesthesia that images the entire colon; recommended every ten years), and double-contrast barium enema (x-ray procedure following barium/air enema; recommended every five years)(18-23). Newer recommendations have added other stool-based testing (e.g., stool DNA tests) and newer imaging techniques (e.g., computerized tomography colonography; 24).
Studies have been done on a number of demographic, social, and environmental determinants of colorectal cancer screening (e.g., insurance coverage, discussion with a medical professional (25-27)). Given that screening ultimately requires behavioral action on the part of the individual person (e.g., going to a colonoscopy appointment; completing and mailing an FOBT card), understanding factors involved in individual decision making regarding screening is necessary to improve upon suboptimal screening compliance. The health behavior literature includes numerous theoretical models that describe factors serving as inputs to individual behavioral choices about engaging in health-related behaviors (28-30). The importance of theory-based approaches for both understanding health behavior and developing behavior change interventions is frequently discussed (28, 31-33).
Previous reviews of the literature on determinants of colorectal cancer screening have included some variables that address individual-level determinants related to engaging in screening tests. However, to our knowledge no previous review has systematically examined the extent to which major theoretical models of individual behavior have been examined in the context of colorectal cancer screening behavior and not all of the constructs commonly examined in such models have been included in past literature reviews. Moreover, the existing reviews are five or more years old. There are, therefore, multiple newer studies that have not previously been reviewed. This is especially true for colonoscopy screening, which was the newest screening test widely used in clinical practice at the time of the last review (25).
The key objective for this systematic review is to examine the state of understanding of how individual-level health behavior models have been addressed in the literature on colorectal cancer screening behavior. The purpose is to provide an assessment of what constructs and theoretical models have and have not been studied, to explore the sufficiency of our examination of these constructs in the context of colorectal cancer screening, and to summarize the support found for the role of such constructs as factors associated with colorectal cancer screening behavior.
The review focuses on decision-making constructs from four key models: the health belief model (34), the theory of planned behavior (35), social cognitive theory (36), and the transtheoretical model (37). These four were selected because they are collectively widely used in the field (28) and have been applied across a range of health-related contexts. Because many health behavior models share common underlying assumptions, constructs from these four models also collectively provide a fairly comprehensive representation of constructs included in other health behavior models (30, 38).
To address these objectives, we conducted a comprehensive search for published empirical studies examining the relation between constructs included in the four models and colorectal cancer screening behavior and/or behavioral intentions. Relevant studies were reviewed and their findings concerning the relation of the constructs and behavioral outcomes were coded. In addition, we examined the relation of a number of methodological, measurement, and population characteristics of the studies to their findings about the relation of constructs and behavioral outcomes.
Method
Literature Review Procedures
Inclusion Criteria
The focus of this review is on the relation between theoretical model-based constructs and behavior. The key pre-defined inclusion criteria were that the article: 1) must include measurement of at least one relevant model construct (see Table 1 for a list of models and constructs included in the search); 2) must include a measurement of either engagement in screening behavior or intention to engage in screening behavior; and 3) must report at least one statistical test of the relation between a relevant construct and behavior or behavioral intentions (either by reporting the inferential statistic used to test the relation or by clearly stating in writing the nature of the relation between the two constructs). Given this focus on relations between model constructs and behavior, only study designs which included a quantitative assessment of the relevant constructs were included; other study designs were excluded (e.g., focus groups; open-ended interview studies). Eligible studies were limited to those published in English language journals and to those published in a peer-reviewed journal (i.e., not a dissertation or a thesis).
Table 1.
Theoretical Models and Constructs Included in the Review
| Theoretical Model | Construct |
|---|---|
| Health Belief Model1 | Severity |
| Susceptibility | |
| Benefits | |
| Barriers | |
| Self-efficacy2 | |
| Theory of Reasoned Action/Theory of Planned Behavior3 | Attitude |
| Social norm | |
| Perceived behavioral control | |
| Social Cognitive Theory | Self-efficacy |
| Response efficacy | |
| Transtheoretical Model4 | Decisional Balance |
| Processes of Change |
The original formulation of the health belief model included severity, susceptibility, benefits, and barriers. Cues to action are also included in some formulations of the model; they are not included in this review because they are a feature of the situation rather than a feature of the individual person's decision-making process.
Self-efficacy (belief in ability to successfully engage in a behavior) is included in some later formulations of the health belief model
The theory of reasoned action includes only attitudes and social norms; perceived behavioral control was added in the theory of planned behavior
Because the transtheoretical model explicitly draws constructs from the other included models, only the decision making construct uniquely labeled by it is included here
Database Search
To retrieve the most complete set of potentially applicable articles, a series of keyword searches was conducted in both MEDLINE and PSYCINFO. An initial search was conducted in November 2007; a second search was conducted in November 2008 to add additional relevant articles published in the time since the initial search. In both databases, searches were based on all possible combinations of a term referring to the screening test (see the “screening test names” column in Table 2 for a complete list) and a term referring to a model construct or full model. For the construct terms, terms were selected to capture the widest possible number of relevant articles. For example, the construct “social norms” is referred to as social norms, subjective norms, and behavioral norms across articles. For this reason, the term “norm” was selected as the key search term as it would capture any of the above synonyms; all search terms were used as “includes” versus “exact” to allow for this wide capture (see “construct/model names” column in Table 2 for a full list). No parameters were set for start date to allow capture of all relevant articles. In addition to this database search, the reference lists for both articles included in the review and previous systematic reviews of colorectal cancer screening were screened for additional possible articles.
Table 2.
Screening behavior, construct, and theoretical model keywords used in literature searches.
| Screening behavior keywords | Construct and model keywords |
|---|---|
| Screening | Benefit |
| Colonoscopy | Barrier |
| (Flexible) Sigmoidoscopy | Decisional balance |
| Fecal Occult Blood Test, FOBT | Advantage |
| Barium Enema | Disadvantage |
| Adherence | Cost |
| Compliance | Severity |
| Behavior | Attitude |
| Intention | Efficacy |
| Norm | |
| Susceptibility | |
| Control | |
| Fear | |
| Risk | |
| Pro | |
| Con | |
| Process of Change (also Processes of Change) | |
| Health belief model | |
| Theory of reasoned action | |
| Theory of planned behavior | |
| Transtheoretical model | |
| Social cognitive theory |
Article Screening Process
Based on the inclusion criteria described above, all of the titles retrieved from these searches were screened by two authors (MK and AB or MK and MZ); abstracts were then retrieved for any title judged as relevant by either author. As with the titles, all abstracts were then screened by two authors and full articles were retrieved and reviewed for any abstracts judged as relevant. Each of the retrieved full articles was screened using the inclusion criteria; this set of inclusion criteria and screening resulted in a final set of 81 papers included in the literature review (a complete list of articles included in the review can be found in the Appendix).
Coding of Relevant Articles
For each of the 81 included articles, multiple aspects of study design, study population, measures for key constructs, and results were coded. All included articles were independently read and coded by two authors (MK and AB or MK and MZ). All disagreements in coding were resolved by discussion.
Study design codings included method of data collection (e.g., telephone, mail survey, in person) and design (e.g., cross-sectional, longitudinal). Population codings included number of participants, race, gender, ethnicity, country of study, and any other notable population features. Measures codings included: specific screening tests assessed, type of behavior measured (intentions versus actual behavior), method for assessing behavior (self-report, chart review), constructs assessed, and method for assessing each included construct. Coding of the study results included nature of the relation (positive relation, negative relation, or no effect) and, where reported, inferential statistics for the test of the relation. In the case of longitudinal studies, wherever possible the relation coded was between assessment of the construct at the initial time point and assessment of the behavior or intention at the follow-up time point. A summary of these design characteristics is reported in Table 3.
Table 3.
Summary of Characteristics of the Reviewed Studies
| Design Feature | Number of Studies |
|---|---|
| Data Collection Strategy | |
| Telephone | 30 |
| 25 | |
| In person | 26 |
| Design | |
| Cross-sectional | 63 |
| Prospective/Longitudinal | 13 |
| Retrospective | 5 |
| Sample Size | |
| Less than 100 | 2 |
| 100-299 | 26 |
| 300-499 | 16 |
| 500-699 | 11 |
| 700 or greater | 22 |
| Gender of Participants | |
| Both genders | 64 |
| Males only | 3 |
| Females Only | 9 |
| Country | |
| United States | 59 |
| Other Country | 20 |
| Behavior measure | |
| Intentions | 15 |
| Actual Behavior | 66 |
| Behavior Assessment Method | |
| Self-report | 47 |
| Chart review | 15 |
Results
How Thoroughly Have Constructs Been Examined?
We first assessed the number of studies examining the relation of each of the studied constructs to behavior or behavioral intentions. The results are presented in Table 4. As can be seen in the table, for the three most common screening tests (FOBT, sigmoidoscopy, colonoscopy), the constructs of benefits, barriers, and perceived susceptibility have been relatively well examined, with each having been assessed in more than 25 studies. However, the evidence base is much sparser for the remaining constructs. Only one study has examined the construct of global evaluative attitudes about the screening behavior, a key construct in the theory of reasoned action/theory of planned behavior. In addition, very few studies have examined perceived severity, social norms, and perceived behavioral control.
TABLE 4.
Coverage of constructs by test type.
| Total Articles | Benefits | Barriers | Susceptibility | Severity | Attitudes | Norms | PBC | |
|---|---|---|---|---|---|---|---|---|
| FOBT | 64 | 35 (55%) | 33 (52%) | 38 (59%) | 12 (19%) | 1 (2%) | 10 (16%) | 9 (14%) |
| SIG | 57 | 34 (60%) | 34 (60%) | 34 (60%) | 10 (18%) | 1 (2%) | 11 (19%) | 8 (14%) |
| COL | 44 | 26 (59%) | 27 (47%) | 25 (44%) | 9 (20%) | 1 (2%) | 7 (16%) | 4 (9%) |
| Barium Enema | 14 | 9 (64%) | 9 (64%) | 11 (79%) | 4 (29%) | 0 (0%) | 3 (21%) | 2 (14%) |
| Other | 9 | 4 (44%) | 6 (67%) | 6 (67%) | 2 (22%) | 0 (0%) | 2 (22%) | 3 (33%) |
Note: numbers in cells indicate the number of published studies which assess the relation of each construct to screening behavior; numbers in parentheses are the percentage of the articles addressing a particular test which include the construct. Test-specific and construct specific numbers add up to more than the total number of articles because many studies address more than one screening test and more than one construct. Tests included under “other” were digital rectal exam (8 studies), Fecal DNA (1 study), and virtual colonoscopy (1 study).
The evidence base also varies considerably by type of screening test. As can be seen in the table, for each construct more studies have examined FOBT than any other screening test, and the numbers of studies are, not surprisingly, especially low for newer screening tests (e.g., Fecal DNA). Even though colonoscopy is frequently used and preferred by many providers, the number of studies assessing colonoscopy is lower than for either FOBT or sigmoidoscopy (this is likely wholly attributable to the fact that introduction and adoption of colonoscopic screening was more recent than either FOBT or sigmoidoscopy).
Finally, we examined how many studies had fully investigated a given theoretical construct (i.e., included all of the constructs from a given theory). This was done for the health belief model, the theory of reasoned action, and the theory of planned behavior (social cognitive theory and the transtheoretical model both include a variety of constructs that do not fall under the parameters for this literature review and thus were not examined in this analysis). Thirteen studies examined all of the constructs in the health belief model, but no studies included all of the constructs from either the theory of reasoned action or the theory of planned behavior.
How Consistent is the Evidence Base with Predictions from Health Behavior Theories?
The second question examined was how well the evidence base in the literature supported the predictions made by the theoretical models. With the exception of perceived barriers, the hypothesis derived from the theoretical models for each construct would be for a positive relation; that is, as attitude or social norms become more positive; as one perceives more personal susceptibility or severity; as one perceives more benefits to the behavior or greater behavioral control over the behavior, likelihood of engaging in the screening behavior should increase. For perceived barriers, a negative or inverse relation is predicted – as one perceives more barriers to engagement in the behavior, the likelihood of engaging in the behavior should decrease.
The number of published studies which found a positive, a negative, or no significant relation between each decision-making construct and behavior or behavioral intentions is reported in Table 5. As can be seen in the table, for each of the investigated constructs the majority of the studies supported the hypotheses derived from the theoretical models. It was virtually never the case that the relation reported was the opposite of the one predicted by the model. However, for each of the constructs except attitudes and social norms, notable minorities of the studies (typically about 1/3) reported no relation between the construct and behavior or behavioral intentions.
Table 5.
Relation of Constructs to Behavior
| Construct | Test | Number of Studies | Relation | ||
|---|---|---|---|---|---|
| | |||||
| Predicted | Opposite of Predicted | No Relation | |||
| Perceived Benefits | FOBT | 35 | 22 | 0 | 13 |
| SIG | 34 | 23 | 0 | 11 | |
| COL | 26 | 18 | 0 | 8 | |
| DCBE | 9 | 6 | 0 | 3 | |
| Other | 4 | 4 | 0 | 0 | |
| | |||||
| Perceived Barriers | FOBT | 33 | 25 | 0 | 8 |
| SIG | 34 | 26 | 1 | 7 | |
| COL | 27 | 19 | 0 | 8 | |
| DCBE | 9 | 6 | 0 | 3 | |
| Other | 6 | 4 | 0 | 2 | |
| | |||||
| Perceived Susceptibility | FOBT | 38 | 22 | 0 | 16 |
| SIG | 34 | 22 | 0 | 12 | |
| COL | 25 | 16 | 0 | 9 | |
| DCBE | 11 | 8 | 0 | 3 | |
| Other | 6 | 5 | 0 | 1 | |
| | |||||
| Perceived Severity | FOBT | 12 | 4 | 2 | 6 |
| SIG | 10 | 1 | 3 | 6 | |
| COL | 9 | 1 | 2 | 6 | |
| DCBE | 4 | 0 | 2 | 2 | |
| Other | 2 | 0 | 2 | 0 | |
| | |||||
| Attitudes | FOBT | 1 | 1 | 0 | 0 |
| SIG | 1 | 1 | 0 | 0 | |
| COL | 1 | 1 | 0 | 0 | |
| DCBE | 0 | 0 | 0 | 0 | |
| Other | 0 | 0 | 0 | 0 | |
| | |||||
| Social Norms | FOBT | 12 | 10 | 0 | 2 |
| SIG | 11 | 11 | 0 | 0 | |
| COL | 7 | 7 | 0 | 0 | |
| DCBE | 3 | 3 | 0 | 0 | |
| Other | 2 | 2 | 0 | 0 | |
| | |||||
| Perceived Behavioral Control | FOBT | 14 | 9 | 0 | 5 |
| SIG | 10 | 8 | 0 | 2 | |
| COL | 6 | 4 | 0 | 2 | |
| DCBE | 3 | 2 | 0 | 1 | |
| Other | 3 | 3 | 0 | 0 | |
Relation of Methodological Features to Study Findings
Given the heterogeneity in findings for each of the constructs’ theory driven predictions, we examined whether methodological features explained differences between studies which found support for the theory- predicted relation versus no support (given the small number, “counter-supportive findings” were excluded from the analysis). To do so, we examined the relation between study design (cross-sectional versus longitudinal – 5 retrospective studies were excluded), type of behavior studied (behavioral intentions versus actual behavior; studies that included both were included as actual behavior), type of behavior measure for actual behavior studied (self-report versus chart review), data collection method (mail, telephone, or in-person survey; three studies that used multiple methods were excluded), gender of participants (male only, female only, or both male and female), age studied (only participants over 50 versus participants both under and over 50), country in which the study was conducted (USA versus other), year of publication (2000 or earlier versus 2001 or later), and sample size (< 250, 251-600, >600). In each case, we used Fisher's exact test (given the small n's in some cells; e.g., longitudinal studies examining social norms) to examine whether the proportion of studies finding the predicted relation differed as a function of the methodological variable. Given the very small number of studies in some categories when broken down by both decision-making variable and type of test, this analysis was conducted aggregating across specific colorectal cancer screening tests (studies which examined more than one screening test were only included once in this analysis). Similar results were found for multivariate analyses.
Design type influenced the findings for severity; longitudinal studies were more likely to show effects; χ2 (1) = 5.92, exact p = 0.04. It also influenced findings for social norms, with cross-sectional studies more likely to show effects; χ2 (1) = 8.56 p = 0.03. There were no other significant effects for design type. Behavior measure strategy influenced findings for perceived risk, with self report studies more likely to show effects; χ2 (1) =8.00, p = 0.008. There were no other significant effects for behavior measure. There were no significant effects for behavior type (intentions versus actual behavior), data collection method, gender inclusion, age range, country, year of publication, or sample size. Given that sample size is a known influence on statistical power (39), we also conducted analyses to see whether sample size (as a continuous variable) significantly differed for those studies which showed a theory-predicted effect relative to those which did not. There was no significant difference for any of the theory-related constructs, all ts < 1.3, ns.
Discussion
The overarching finding from this literature review is that, by and large, constructs from health behavior models are associated with colorectal cancer screening behavior. For each of the constructs except perceived severity, the majority of included studies found showed support for the theory-derived, predicted relation between the construct and screening behavior. Given that none of these theoretical models were developed specifically in the colorectal cancer screening context and that screening behavior has a number of features which differentiate it from other types of health behaviors, the observation that the models are effective at accounting for screening behavior is an important one for our understanding of how individuals make decisions about colorectal cancer screening. These models are frequently suggested as starting points for developing interventions to change behaviors (28, 40-41), so knowledge of their effectiveness at accounting for screening decisions is an important precondition for designing effective interventions.
However, although the majority of studies examining a given construct found support for the theory-derived predictions and few or no studies found the opposite relation, a notable minority of studies found no relation. The reason for this heterogeneity in findings remains unexplained -- the difference in findings was not due to sample size, methodological, participant, or measurement characteristics examined in the literature review.
What do we know about the degree of research coverage of health behavior theories in the context of colorectal cancer screening behavior? First, although numerous studies have looked at one or more constructs from formal health behavior models, the degree to which constructs have been examined as influences on screening varies widely. Perceived benefits and perceived barriers have been fairly well examined in the literature, but significantly less attention has been given to other important behavioral influences, especially attitudes about the behavior and perceptions of social norms regarding the behavior. Moreover, very few studies have examined all of the constructs in a given theoretical model and only the health belief model has been fully examined within the context of a single study.
This is an important limitation to the literature. The constructs examined are all parts of well-developed theoretical models and their utility for understanding behavior has been demonstrated in numerous other health behavior contexts. However, it may not be the case that constructs are equivalently applicable across behaviors, and thus examining the utility of each construct for understanding and addressing colorectal cancer screening behavior is a remaining research need. Moreover, one cannot necessarily assume that decision-making processes will work equivalently across screening tests. For example, issues around self-efficacy/perceived behavioral control may be stronger for colonoscopy, which involves a relatively complicated, self-directed preparation protocol to be followed for successful screening. In addition to being a research limitation, the issue of coverage of constructs and tests is a limitation for clinical application of study findings. In other domains, interventions based on constructs such as social norms and self-efficacy have been effective at changing behavior. Such interventions may be effective for colorectal cancer screening behavior as well, but without a base of knowledge about the influence of the constructs on behavior it is difficult to predict the likely effect of such interventions.
Issues in the Literature
This summary of findings raises a number of issues of concern in the literature: the unexplained heterogeneity in findings, relative scarcity of research coverage of some decision making constructs for some tests, and piecemeal selection of constructs from models. In addition to these issues which arise directly from the findings of the literature review, some additional concerns were observed in the course of conducting the review of the literature.
First, it was observed that there is a substantial lack of consistency in how constructs are conceptually and operationally defined and how they are labeled. In several cases, an article stated that a construct from one of the included models was assessed, but closer inspection of the measure used revealed that the way the construct was defined differed in substantive ways from the conceptual definition in the given model. For example, several studies were excluded because they stated that attitudes toward the screening procedure were measured but had operational definitions of attitude that did not mesh with the common conceptual definition. In the decision-making literature, one's attitude toward a behavior is the overall evaluation one has of the behavior (e.g., whether one evaluates it positively or negatively(42)). Several articles included in the review included an “attitudes” construct but actually assessed other decision-making constructs (e.g., perceived benefits and barriers; 43) or the emotions one would anticipate experiencing if one were screened (e.g., embarrassment; 44). Although both of these are potentially important influences on decision making about screening, neither captures the conceptual definition of the attitudes construct (42, 45). In a related vein, the commonly included construct of salience and coherence of screening (46-47) mixes multiple conceptual constructs in a single scale factor. The measure includes questions which tap into benefits, social norms, perceived behavioral control, and attitudes.
A second issue emerged even among studies which qualified for inclusion in the review. Within studies assessing a given construct, there was substantial variability in how authors chose to operationalize the constructs. For example, for the construct of perceived susceptibility, some studies assessed absolute risk (e.g., one's rating of one's own chances of experiencing cancer), some assessed comparative risk (e.g., one's chances relative to others), and some studies included both. Although both absolute and comparative risk are important constructs, they are separate and distinct and can have different influences on decision making (48). Similar heterogeneity in operational definitions was observed for many of the other constructs assessed. Thus, conclusions about when and how a given construct influences behavior may be, in part, influenced by how the construct was operationalized. Recent attempts to develop standardized measurement tools for assessing constructs for colorectal cancer screening (e.g., 49) and for measures of screening behavior (e.g., 50) may attenuate this problem over time, but such measures do not include all of the constructs assessed in this review and are not yet widely used in the literature. This problem of lack of standardization at both the conceptual and the operational level is an important one to address. To the extent that we lack standard conceptual definitions of constructs, it may be the case that different researchers are really examining different constructs and that interventionists trying to address the relevant health behavior issues may be intervening on different constructs. Use of standardized conceptual definitions for constructs (for example, using definitions of constructs in standard health behavior theory texts(28) or web resources(51)) would be of benefit for advancing the field.
Limitations
Limitations to the review must, of course, be taken into consideration. First we elected a somewhat constrained focus on concepts related to a set of well-established individual-level health behavior models. This choice was both conceptual and practical. Conceptually, given our focus on individual behavior, such selection provided and captures the state of our understanding of constructs related to colorectal cancer screening. Practically, these models often guide both research on screening and interventions to change screening behavior, and thus the inclusion strategy effectively captures the state of the literature. The downside of this choice, of course, is that such a strategy fails to capture more “piecemeal” constructs, which might be part of individuals’ behavioral choices but are not captured in a full-fledged theoretical model. The strategy also excludes some constructs (like salience and coherence) that map across constructs in a particular theoretical model (see discussion above about salience and coherence).
Second, the review is naturally limited by the number of studies available. Although at the broadest aggregate level there are a number of studies examining the relation of these constructs to colorectal cancer screening, there is a paucity of studies when one narrows down to the level of particular tests and particular constructs. This relatively small number of studies should be considered when interpreting the reported results (e.g., the findings of no relation between design features and study outcomes might be influenced by the relatively small number of studies). It is also the case that, as with all reviews of the published literature, the number of studies involved also relates to the possibility of publication bias. Because studies which find effects are more likely to be published, this bias should be considered when interpreting the findings.
Third, the review took a narrative, descriptive approach to summarizing research findings rather than a quantitative, meta-analytic approach. This decision was largely driven by the state of the research literature; we conducted data coding in a way that would have allowed for a meta-analysis, but found that only a small subset of the relevant studies reported sufficient statistical information to allow for inclusion in a meta-analysis. Given this, we elected to use an approach which allowed for a broader inclusion of studies. However, it should be acknowledged that there would be information available in a meta-analytic approach not available in this descriptive review.
Finally, although we coded and analyzed a number of methodological and participant factors for each study and examined their effect on study findings, there are other potential study features (e.g., other aspects of study populations; specific measurement operationalizations of constructs) which were not consistently reported in articles but which might help to explain some of the heterogeneity in study findings.
Conclusion
Colorectal cancer is a serious contributor to disease morbidity and mortality. Multiple screening tests are available for early detection of colorectal cancer, but population adherence to screening recommendations for these tests is limited. Our review of the literature of studies examining individual-level decision factors related to engagement in these tests revealed that, for the most part studies supported the utility of existing, formal health behavior models as account for colorectal cancer screening behavior. However, the evidence base for decisions about many of these tests is quite limited, especially when one moves past the health belief model to examine other theoretical frameworks for understanding health related behaviors, including screening. Future research should seek to broaden the evidence base for the factors which influence compliance with colorectal cancer screening, should consider use of common measurement tools to enable better comparisons across studies, should examine the consistencies and differences in factors which influence decisions and behaviors for each of the variety of screening tests available for colorectal cancer, and should consider the extent to which findings of colorectal cancer screening tests are consistent across populations. Given the substantial public health costs of colorectal cancer and the availability of tests for early detection and prevention, such examination of health behaviors could be a substantial contributor to better understanding noncompliance to screening recommendations, therefore addressing the population burden of colorectal cancer.
Acknowledgments
Research supported by NCI grant K07CA106225 to Marc T. Kiviniemi
Appendix: Articles Included In Review
- Azaiza F, Cohen M. Colorectal cancer screening, intentions, and predictors in Jewish and Arab Israelis: a population-based study. Health Educ Behav. 2008;35:478–493. doi: 10.1177/1090198106297045. [DOI] [PubMed] [Google Scholar]
- Berkowitz Z, Hawkins NA, Peipins LA, White MC, Nadel MR. Beliefs, risk perceptions, and gaps in knowledge as barriers to colorectal cancer screening in older adults. J Am Geriatr Soc. 2008;56:307–314. doi: 10.1111/j.1532-5415.2007.01547.x. [DOI] [PubMed] [Google Scholar]
- Blalock SJ, DeVellis BM, Afifi RA, Sandler RS. Risk perceptions and participation in colorectal cancer screening. Health Psychol. 1990;9:792–806. doi: 10.1037//0278-6133.9.6.792. [DOI] [PubMed] [Google Scholar]
- Bleiker EMA, Menko FH, Taal BG, Kluijt I, Wever LDV, Gerritsma MA, et al. Screening behavior of individuals at high risk for colorectal cancer. Gastroenterology. 2005;128:280–287. doi: 10.1053/j.gastro.2004.11.002. [DOI] [PubMed] [Google Scholar]
- Brawarsky P, Brooks DR, Mucci LA. Correlates of colorectal cancer testing in Massachusetts men and women. Prev Med. 2003;36:659–668. doi: 10.1016/s0091-7435(03)00046-x. [DOI] [PubMed] [Google Scholar]
- Brenes GA, Paskett ED. Predictors of stage of adoption for colorectal cancer screening. Prev Med. 2000;31:410–416. doi: 10.1006/pmed.2000.0729. [DOI] [PubMed] [Google Scholar]
- Burack RC, Liang J. The early detection of cancer in the primary-care setting: factors associated with the acceptance and completion of recommended procedures. Prev Med. 1987;16:739–751. doi: 10.1016/0091-7435(87)90014-4. [DOI] [PubMed] [Google Scholar]
- Christie J, Hooper C, Redd WH, Winkel G, DuHamel K, Itzkowitz S, et al. Predictors of endoscopy in minority women. J Natl Med Assoc. 2005;97:1361–1368. [PMC free article] [PubMed] [Google Scholar]
- Christie J, Nassisi D, Wilets I, DuHamel KN, Winkel G, Hilliard R, et al. Assessing endoscopic colorectal screening adherence in an emergency department population. J Natl Med Assoc. 2006;98:1095–1101. [PMC free article] [PubMed] [Google Scholar]
- Codori AM, Petersen GM, Miglioretti DL, Boyd P. Health beliefs and endoscopic screening for colorectal cancer: potential for cancer prevention. Prev Med. 2001;33:128–136. doi: 10.1006/pmed.2001.0862. [DOI] [PubMed] [Google Scholar]
- Collins V, Meiser B, Gaff C, St John DJB, Halliday J. Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma. Cancer. 2005;104:273–281. doi: 10.1002/cncr.21183. [DOI] [PubMed] [Google Scholar]
- Costanza ME, Luckmann R, Stoddard AM, Avrunin JS, White MJ, Stark JR, et al. Applying a stage model of behavior change to colon cancer screening. Prev Med. 2005;41:707–719. doi: 10.1016/j.ypmed.2004.12.013. [DOI] [PubMed] [Google Scholar]
- Cronan TA, Devos-Comby L, Villalta I, Gallagher R. Ethnic differences in colorectal cancer screening. J Psychosoc Oncol. 2008;26:63–86. doi: 10.1300/j077v26n02_05. [DOI] [PubMed] [Google Scholar]
- Farmer MM, Bastani R, Kwan L, Belman M, Ganz PA. Predictors of colorectal cancer screening from patients enrolled in a managed care health plan. Cancer. 2008;112:1230–1238. doi: 10.1002/cncr.23290. [DOI] [PubMed] [Google Scholar]
- Farraye FA, Wong M, Hurwitz S, Puleo E, Emmons K, Wallace MB, et al. Barriers to endoscopic colorectal cancer screening: are women different from men? Am J Gastroenterol. 2004;99:341–349. doi: 10.1111/j.1572-0241.2004.04045.x. [DOI] [PubMed] [Google Scholar]
- Frank D, Swedmark J, Grubbs L. Colon cancer screening in African American women. Abnf J. 2004;15:67–70. [PubMed] [Google Scholar]
- Frew E, Wolstenholme J, Whynes D. Mass population screening for colorectal cancer: factors influencing subjects’ choice of screening test. J Health Serv Res Policy. 2001;6:85–91. doi: 10.1258/1355819011927279. [DOI] [PubMed] [Google Scholar]
- Friedman LC, Everett TE, Peterson L, Ogbonnaya KI, Mendizabal V. Compliance with fecal occult blood test screening among low-income medical outpatients: a randomized controlled trial using a videotaped intervention. J Cancer Educ. 2001;16:85–88. doi: 10.1080/08858190109528738. [DOI] [PubMed] [Google Scholar]
- Friedman LC, Puryear LJ, Moore A, Green CE. Breast and colorectal cancer screening among low-income women with psychiatric disorders. Psychooncology. 2005;14:786–791. doi: 10.1002/pon.906. [DOI] [PubMed] [Google Scholar]
- Friedman LC, Webb JA, Everett TE. Psychosocial and medical predictors of colorectal cancer screening among low-income medical outpatients. J Cancer Educ. 2004;19:180–186. doi: 10.1207/s15430154jce1903_14. [DOI] [PubMed] [Google Scholar]
- Friedman LC, Webb JA, Richards CS, Plon SE. Psychological and behavioral factors associated with colorectal cancer screening among Ashkenazim. Prev Med. 1999;29:119–125. doi: 10.1006/pmed.1999.0508. [DOI] [PubMed] [Google Scholar]
- Giorgi Rossi P, Federici A, Bartolozzi F, Farchi S, Borgia P, Guasticchi G. Understanding non-compliance to colorectal cancer screening: a case control study, nested in a randomised trial [ISRCTN83029072]. BMC Public Health. 2005;5:139. doi: 10.1186/1471-2458-5-139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorin SS. Correlates of colorectal cancer screening compliance among urban Hispanics. J Behav Med. 2005;28:125–137. doi: 10.1007/s10865-005-3662-5. [DOI] [PubMed] [Google Scholar]
- Green PM, Kelly BA. Colorectal cancer knowledge, perceptions, and behaviors in African Americans. Cancer Nurs. 2004;27:206–215. doi: 10.1097/00002820-200405000-00004. quiz 216-207. [DOI] [PubMed] [Google Scholar]
- Harewood GC, Wiersema MJ, Melton LJ., 3rd A prospective, controlled assessment of factors influencing acceptance of screening colonoscopy. Am J Gastroenterol. 2002;97:3186–3194. doi: 10.1111/j.1572-0241.2002.07129.x. [DOI] [PubMed] [Google Scholar]
- Harris MA, Byles JE. A survey of screening compliance among first degree relatives of people with colon cancer in New South Wales. J Med Screen. 1997;4:29–34. doi: 10.1177/096914139700400110. [DOI] [PubMed] [Google Scholar]
- Hay JL, Ford JS, Klein D, Primavera LH, Buckley TR, Stein TR, et al. Adherence to colorectal cancer screening in mammography-adherent older women. J Behav Med. 2003;26:553–576. doi: 10.1023/a:1026253802962. [DOI] [PubMed] [Google Scholar]
- Helzlsouer KJ, Ford DE, Hayward RS, Midzenski M, Perry H. Perceived risk of cancer and practice of cancer prevention behaviors among employees in an oncology center. Prev Med. 1994;23:302–308. doi: 10.1006/pmed.1994.1042. [DOI] [PubMed] [Google Scholar]
- Honda K, Kagawa-Singer M. Cognitive mediators linking social support networks to colorectal cancer screening adherence. J Behav Med. 2006;29:449–460. doi: 10.1007/s10865-006-9068-1. [DOI] [PubMed] [Google Scholar]
- Hoogewerf PE, Hislop TG, Morrison BJ, Burns SD, Sizto R. Health belief and compliance with screening for fecal occult blood. Soc Sci Med. 1990;30:721–726. doi: 10.1016/0277-9536(88)90257-2. [DOI] [PubMed] [Google Scholar]
- Hou S, Chen P. Cancer screening beliefs and reactions to an innovative colorectal cancer screening kit among Chinese worksite population. Methods Inf Med. 2005;44:315–318. [PubMed] [Google Scholar]
- James AS, Campbell MK, Hudson MA. Perceived barriers and benefits to colon cancer screening among African Americans in North Carolina: how does perception relate to screening behavior? Cancer Epidemiol Biomarkers Prev. 2002;11:529–534. [PubMed] [Google Scholar]
- Janda M, Stanton WR, Hughes K, Del Mar C, Clavarino A, Aitken JF, et al. Knowledge, attitude and intentions related to colorectal cancer screening using faecal occult blood tests in a rural Australian population. Asia Pac J Public Health. 2003;15:50–56. doi: 10.1177/101053950301500109. [DOI] [PubMed] [Google Scholar]
- Jansen JH. Participation in the first and second round of a mass-screening for colorectal cancer. Soc Sci Med. 1984;18:633–636. doi: 10.1016/0277-9536(84)90291-0. [DOI] [PubMed] [Google Scholar]
- Janz NK, Lakhani I, Vijan S, Hawley ST, Chung LK, Katz SJ. Determinants of colorectal cancer screening use, attempts, and non-use. Prev Med. 2007;44:452–458. doi: 10.1016/j.ypmed.2006.04.004. [DOI] [PubMed] [Google Scholar]
- Janz NK, Wren PA, Schottenfeld D, Guire KE. Colorectal cancer screening attitudes and behavior: a population-based study. Prev Med. 2003;37:627–634. doi: 10.1016/j.ypmed.2003.09.016. [DOI] [PubMed] [Google Scholar]
- Kelly RB, Shank JC. Adherence to screening flexible sigmoidoscopy in asymptomatic patients. Med Care. 1992;30:1029–1042. doi: 10.1097/00005650-199211000-00006. [DOI] [PubMed] [Google Scholar]
- Kim SE, Perez-Stable EJ, Wong S, Gregorich S, Sawaya GF, Walsh JME, et al. Association between cancer risk perception and screening behavior among diverse women. Arch Intern Med. 2008;168:728–734. doi: 10.1001/archinte.168.7.728. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kinney AY, Hicken B, Simonsen SE, Venne V, Lowstuter K, Balzotti J, et al. Colorectal cancer surveillance behaviors among members of typical and attenuated FAP families. Am J Gastroenterol. 2007;102:153–162. doi: 10.1111/j.1572-0241.2006.00860.x. [DOI] [PubMed] [Google Scholar]
- Kremers SP, Mesters I, Pladdet IE, van den Borne B, Stockbrugger RW. Participation in a sigmoidoscopic colorectal cancer screening program: a pilot study. Cancer Epidemiol Biomarkers Prev. 2000;9:1127–1130. [PubMed] [Google Scholar]
- Lawsin C, DuHamel K, Weiss A, Rakowski W, Jandorf L. Colorectal cancer screening among low-income African Americans in East Harlem: a theoretical approach to understanding barriers and promoters to screening. J Urban Health. 2007;84:32–44. doi: 10.1007/s11524-006-9126-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lewis SF, Jensen NM. Screening sigmoidoscopy. Factors associated with utilization. J Gen Intern Med. 1996;11:542–544. doi: 10.1007/BF02599602. [DOI] [PubMed] [Google Scholar]
- Lipkus IM, Green LG, Marcus A. Manipulating perceptions of colorectal cancer threat: implications for screening intentions and behaviors. J Health Commun. 2003;8:213–228. doi: 10.1080/10810730305684. [DOI] [PubMed] [Google Scholar]
- Lipkus IM, Lyna PR, Rimer BK. Colorectal cancer risk perceptions and screening intentions in a minority population. J Natl Med Assoc. 2000;92:492–500. [PMC free article] [PubMed] [Google Scholar]
- Macrae FA, Hill DJ, St John DJ, Ambikapathy A, Garner JF. Predicting colon cancer screening behavior from health beliefs. Prev Med. 1984;13:115–126. doi: 10.1016/0091-7435(84)90044-6. [DOI] [PubMed] [Google Scholar]
- Madlensky L, Esplen MJ, Gallinger S, McLaughlin JR, Goel V. Relatives of colorectal cancer patients: factors associated with screening behavior. Am J Prev Med. 2003;25:187–194. doi: 10.1016/s0749-3797(03)00202-2. [DOI] [PubMed] [Google Scholar]
- Mandelson MT, Curry SJ, Anderson LA, Nadel MR, Lee NC, Rutter CM, et al. Colorectal cancer screening participation by older women. Am J Prev Med. 2000;19:149–154. doi: 10.1016/s0749-3797(00)00193-8. [DOI] [PubMed] [Google Scholar]
- Manne S, Markowitz A, Winawer S, Guillem J, Meropol NJ, Haller D, et al. Understanding intention to undergo colonoscopy among intermediate-risk siblings of colorectal cancer patients: a test of a mediational model. Prev Med. 2003;36:71–84. doi: 10.1006/pmed.2002.1122. [DOI] [PubMed] [Google Scholar]
- Manne S, Markowitz A, Winawer S, Meropol NJ, Haller D, Rakowski W, et al. Correlates of colorectal cancer screening compliance and stage of adoption among siblings of individuals with early onset colorectal cancer. Health Psychol. 2002;21:3–15. [PubMed] [Google Scholar]
- Matthews BA, Nattinger AB, Venkatesan T, Shaker R. Colorectal cancer screening among midwestern community-based residents: indicators of success. J Community Health. 2007;32:103–120. doi: 10.1007/s10900-006-9038-0. [DOI] [PubMed] [Google Scholar]
- Matthews BA, Nattinger AB, Venkatesan T, Shaker R, Anderson RC. Objective risk, subjective risk, and colorectal cancer screening among a clinic sample. Psychology, Health & Medicine. 2007;12:135–147. doi: 10.1080/13548500500429312. [DOI] [PubMed] [Google Scholar]
- McQueen A, Vernon SW, Meissner HI, Klabunde CN, Rakowski W. Are there gender differences in colorectal cancer test use prevalence and correlates? Cancer Epidemiol Biomarkers Prev. 2006;15:782–791. doi: 10.1158/1055-9965.EPI-05-0629. [DOI] [PubMed] [Google Scholar]
- McQueen A, Vernon SW, Myers RE, Watts BG, Lee ES, Tilley BC. Correlates and predictors of colorectal cancer screening among male automotive workers. Cancer Epidemiol Biomarkers Prev. 2007;16:500–509. doi: 10.1158/1055-9965.EPI-06-0757. [DOI] [PubMed] [Google Scholar]
- Menon U, Belue R, Sugg Skinner C, Rothwell BE, Champion V. Perceptions of colon cancer screening by stage of screening test adoption. Cancer Nurs. 2007;30:178–185. doi: 10.1097/01.NCC.0000270706.80037.05. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Menon U, Champion VL, Larkin GN, Zollinger TW, Gerde PM, Vernon SW. Beliefs associated with fecal occult blood test and colonoscopy use at a worksite colon cancer screening program. J Occup Environ Med. 2003;45:891–898. doi: 10.1097/01.jom.0000083038.56116.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Montano DE, Selby JV, Somkin CP, Bhat A, Nadel M. Acceptance of flexible sigmoidoscopy screening for colorectal cancer. Cancer Detect Prev. 2004;28:43–51. doi: 10.1016/j.cdp.2003.11.005. [DOI] [PubMed] [Google Scholar]
- Moser RP, McCaul K, Peters E, Nelson W, Marcus SE. Associations of perceived risk and worry with cancer health-protective actions: data from the Health Information National Trends Survey (HINTS). J Health Psychol. 2007;12:53–65. doi: 10.1177/1359105307071735. [DOI] [PubMed] [Google Scholar]
- Myers RE, Ross E, Jepson C, Wolf T, Balshem A, Millner L, et al. Modeling adherence to colorectal cancer screening. Prev Med. 1994;23:142–151. doi: 10.1006/pmed.1994.1020. [DOI] [PubMed] [Google Scholar]
- Myers RE, Vernon SW, Tilley BC, Lu M, Watts BG. Intention to screen for colorectal cancer among white male employees. Prev Med. 1998;27:279–287. doi: 10.1006/pmed.1998.0264. [DOI] [PubMed] [Google Scholar]
- Ng EST, Tan CH, Teo DCL, Seah CYE, Phua KH. Knowledge and perceptions regarding colorectal cancer screening among Chinese--a community-based survey in Singapore. Prev Med. 2007;45:332–335. doi: 10.1016/j.ypmed.2007.06.021. [DOI] [PubMed] [Google Scholar]
- Palmer RC, Emmons KM, Fletcher RH, Lobb R, Miroshnik I, Kemp JA, et al. Familial risk and colorectal cancer screening health beliefs and attitudes in an insured population. Prev Med. 2007;45:336–341. doi: 10.1016/j.ypmed.2007.07.021. [DOI] [PubMed] [Google Scholar]
- Paskett ED, Rushing J, D'Agostino R, Jr., Tatum C, Velez R. Cancer screening behaviors of low-income women: the impact of race. Womens Health. 1997;3:203–226. [PubMed] [Google Scholar]
- Price JH. Perceptions of colorectal cancer in a socioeconomically disadvantaged population. J Community Health. 1993;18:347–362. doi: 10.1007/BF01323966. [DOI] [PubMed] [Google Scholar]
- Rawl SM, Menon U, Champion VL, May FE, Loehrer P, Sr., Hunter C, et al. Do benefits and barriers differ by stage of adoption for colorectal cancer screening? Health Educ Res. 2005;20:137–148. doi: 10.1093/her/cyg110. [DOI] [PubMed] [Google Scholar]
- Sandler RS, DeVellis BM, Blalock SJ, Holland KL. Participation of high-risk subjects in colon cancer screening. Cancer. 1989;63:2211–2215. doi: 10.1002/1097-0142(19890601)63:11<2211::aid-cncr2820631125>3.0.co;2-q. [DOI] [PubMed] [Google Scholar]
- Shokar NK, Carlson CA, Weller SC. Factors associated with racial/ethnic differences in colorectal cancer screening. J Am Board Fam Med. 2008;21:414–426. doi: 10.3122/jabfm.2008.05.070266. [DOI] [PubMed] [Google Scholar]
- Spector MH, Applegate WB, Olmstead SJ, DiVasto PV, Skipper B. Assessment of attitudes toward mass screening for colorectal cancer and polyps. Preventive Medicine. 1981;10:105–109. doi: 10.1016/0091-7435(81)90011-6. [DOI] [PubMed] [Google Scholar]
- Straus WL, Mansley EC, Gold KF, Wang Q, Reddy P, Pashos CL. Colorectal cancer screening attitudes and practices in the general population: a risk-adjusted survey. J Public Health Manag Pract. 2005;11:244–251. doi: 10.1097/00124784-200505000-00010. [DOI] [PubMed] [Google Scholar]
- Sun WY, Basch CE, Wolf RL, Li XJ. Factors associated with colorectal cancer screening among Chinese-Americans. Prev Med. 2004;39:323–329. doi: 10.1016/j.ypmed.2004.04.029. [DOI] [PubMed] [Google Scholar]
- Sung JJY, Choi SYP, Chan FKL, Ching JYL, Lau JTF, Griffiths S. Obstacles to colorectal cancer screening in Chinese: a study based on the health belief model. Am J Gastroenterol. 2008;103:974–981. doi: 10.1111/j.1572-0241.2007.01649.x. [DOI] [PubMed] [Google Scholar]
- Sutton S, Wardle J, Taylor T, McCaffery K, Williamson S, Edwards R, et al. Predictors of attendance in the United Kingdom flexible sigmoidoscopy screening trial. J Med Screen. 2000;7:99–104. doi: 10.1136/jms.7.2.99. [DOI] [PubMed] [Google Scholar]
- Tessaro I, Mangone C, Parkar I, Pawar V. Knowledge, barriers, and predictors of colorectal cancer screening in an Appalachian church population. Prev Chronic Dis. 2006;3:A123. [PMC free article] [PubMed] [Google Scholar]
- Tong S, Hughes K, Oldenburg BB, Mar CD. Colorectal cancer screening with faecal occult blood testing: community intention, knowledge, beliefs and behaviour. Asia Pac J Public Health. 2006;18:16–23. doi: 10.1177/10105395060180010401. [DOI] [PubMed] [Google Scholar]
- Vernon SW, Myers RE, Tilley BC, Li S. Factors associated with perceived risk in automotive employees at increased risk of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2001;10:35–43. [PubMed] [Google Scholar]
- Wardle J, Sutton S, Williamson S, Taylor T, McCaffery K, Cuzick J, et al. Psychosocial influences on older adults’ interest in participating in bowel cancer screening. Prev Med. 2000;31:323–334. doi: 10.1006/pmed.2000.0725. [DOI] [PubMed] [Google Scholar]
- Watts BG, Vernon SW, Myers RE, Tilley BC. Intention to be screened over time for colorectal cancer in male automotive workers. Cancer Epidemiol Biomarkers Prev. 2003;12:339–349. [PubMed] [Google Scholar]
- Weinberg DS, Turner BJ, Wang H, Myers RE, Miller S. A survey of women regarding factors affecting colorectal cancer screening compliance. Prev Med. 2004;38:669–675. doi: 10.1016/j.ypmed.2004.02.015. [DOI] [PubMed] [Google Scholar]
- Weller DP, Owen N, Hiller JE, Willson K, Wilson D. Colorectal cancer and its prevention: prevalence of beliefs, attitudes, intentions and behaviour. Aust J Public Health. 1995;19:19–23. doi: 10.1111/j.1753-6405.1995.tb00291.x. [DOI] [PubMed] [Google Scholar]
- Yepes-Rios M, Reimann JOF, Talavera AC, Ruiz de Esparza A, Talavera GA. Colorectal cancer screening among Mexican Americans at a community clinic. Am J Prev Med. 2006;30:204–210. doi: 10.1016/j.amepre.2005.11.002. [DOI] [PubMed] [Google Scholar]
- Zheng Y-F, Saito T, Takahashi M, Ishibashi T, Kai I. Factors associated with intentions to adhere to colorectal cancer screening follow-up exams. BMC Public Health. 2006;6:272. doi: 10.1186/1471-2458-6-272. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zimmerman RK, Tabbarah M, Trauth J, Nowalk MP, Ricci EM. Predictors of lower endoscopy use among patients at three inner-city neighborhood health centers. J Urban Health. 2006;83:221–230. doi: 10.1007/s11524-005-9028-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
Footnotes
CONFLICT OF INTEREST STATEMENT: The authors declare that there are no conflicts of interest.
References
- 1.Jemal A, Siegel R, Ward E, Hao Y, Xu J, Murray T, et al. Cancer statistics, 2008. CA Cancer J Clin. 2008;58(2):71–96. doi: 10.3322/CA.2007.0010. [DOI] [PubMed] [Google Scholar]
- 2.World Health Organization . Cancer: Fact Sheet #297. World Health Organization; 2006. [Google Scholar]
- 3.Pignone M, Saha S, Hoerger T, Mandelblatt J. Cost-effectiveness analyses of colorectal cancer screening: a systematic review for the U.S. Preventive Services Task Force. Annals of Internal Medicine. 2002;137(2):96–104. doi: 10.7326/0003-4819-137-2-200207160-00007. [DOI] [PubMed] [Google Scholar]
- 4.Kronborg O, Fenger C, Olsen J, Jorgensen OD, Sondergaard O. Randomised study of screening for colorectal cancer with faecal-occult-blood test. Lancet. 1996;348(9040):1467–71. doi: 10.1016/S0140-6736(96)03430-7. [DOI] [PubMed] [Google Scholar]
- 5.Mandel JS, Church TR, Ederer F, Bond JH. Colorectal cancer mortality: effectiveness of biennial screening for fecal occult blood. Journal of the National Cancer Institute. 1999;91(5):434–7. doi: 10.1093/jnci/91.5.434. [DOI] [PubMed] [Google Scholar]
- 6.Muller AD, Sonnenberg A. Protection by endoscopy against death from colorectal cancer. A case-control study among veterans. Archives of Internal Medicine. 1995;155(16):1741–8. doi: 10.1001/archinte.1995.00430160065007. [DOI] [PubMed] [Google Scholar]
- 7.Newcomb PA, Norfleet RG, Storer BE, Surawicz TS, Marcus PM. Screening sigmoidoscopy and colorectal cancer mortality. Journal of the National Cancer Institute. 1992;84(20):1572–5. doi: 10.1093/jnci/84.20.1572. [DOI] [PubMed] [Google Scholar]
- 8.Thiis-Evensen E, Hoff GS, Sauar J, Langmark F, Majak BM, Vatn MH. Population-based surveillance by colonoscopy: effect on the incidence of colorectal cancer. Telemark Polyp Study I. Scandinavian Journal of Gastroenterology. 1999;34(4):414–20. doi: 10.1080/003655299750026443. [DOI] [PubMed] [Google Scholar]
- 9.Walsh JME, Terdiman JP. Colorectal cancer screening: scientific review. JAMA. 2003;289(10):1288–96. doi: 10.1001/jama.289.10.1288. [DOI] [PubMed] [Google Scholar]
- 10.Meissner HI, Breen N, Klabunde CN, Vernon SW. Patterns of colorectal cancer screening uptake among men and women in the United States. Cancer Epidemiology, Biomarkers, and Prevention. 2006;15(2):389–94. doi: 10.1158/1055-9965.EPI-05-0678. [DOI] [PubMed] [Google Scholar]
- 11.Nadel MR, Blackman DK, Shapiro JA, Seeff LC. Are people being screened for colorectal cancer as recommended? Results from the National Health Interview Survey. Preventive Medicine. 2002;35(3):199–206. doi: 10.1006/pmed.2002.1070. [DOI] [PubMed] [Google Scholar]
- 12.Shapiro JA, Seeff LC, Thompson TD, Nadel MR, Klabunde CN, Vernon SW. Colorectal cancer test use from the 2005 National Health Interview Survey. Cancer Epidemiol Biomarkers Prev. 2008;17(7):1623–30. doi: 10.1158/1055-9965.EPI-07-2838. [DOI] [PubMed] [Google Scholar]
- 13.Centers for Disease Control and Prevention Increased use of colorectal cancer tests--United States, 2002 and 2004. Morbidity and Mortality Weekly Report. 2006;55(11):308–11. [PubMed] [Google Scholar]
- 14.Vogelaar I, Ballegooijen Mv, Schrag D, Boer R, Winawer SJ, Habbema DF, et al. How much can current interventions reduce colorectal cancer mortality in the U.S.? Cancer. 2006;107(7):1624–1633. doi: 10.1002/cncr.22115. [DOI] [PubMed] [Google Scholar]
- 15.Lance P. Colorectal cancer screening: confusion reigns. Cancer Epidemiol Biomarkers Prev. 2008;17(9):2205–7. doi: 10.1158/1055-9965.EPI-08-0688. [DOI] [PubMed] [Google Scholar]
- 16.Zauber AG, Lansdorp-Vogelaar I, Knudsen AB, Wilschut J, van Ballegooijen M, Kuntz KM. Evaluating test strategies for colorectal cancer screening: a decision analysis for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;149(9):659–69. doi: 10.7326/0003-4819-149-9-200811040-00244. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Fenton JJ, Cai Y, Green P, Beckett LA, Franks P, Baldwin L- M. Trends in colorectal cancer testing among Medicare subpopulations. Am J Prev Med. 2008;35(3):194–202. doi: 10.1016/j.amepre.2008.05.029. [DOI] [PubMed] [Google Scholar]
- 18.Levin B, Smith RA, Feldman GE, Colditz GA, Fletcher RH, Nadel M, et al. Promoting early detection tests for colorectal carcinoma and adenomatous polyps: a framework for action: the strategic plan of the National Colorectal Cancer Roundtable. Cancer. 2002;95(8):1618–28. doi: 10.1002/cncr.10890. [DOI] [PubMed] [Google Scholar]
- 19.Pignone M, Rich M, Teutsch SM, Berg AO, Lohr KN. Screening for colorectal cancer in adults at average risk: a summary of the evidence for the U.S. Preventive Services Task Force. Annals of Internal Medicine. 2002;137(2):132–41. doi: 10.7326/0003-4819-137-2-200207160-00015. [DOI] [PubMed] [Google Scholar]
- 20.Smith RA, Cokkinides V, Eyre HJ. Cancer Screening in the United States, 2007: A Review of Current Guidelines, Practices, and Prospects. CA: A Cancer Journal for Clinicians. 2007;57(2):90–104. doi: 10.3322/canjclin.57.2.90. [DOI] [PubMed] [Google Scholar]
- 21.Smith RA, von Eschenbach AC, Wender R, Levin B, Byers T, Rothenberger D, et al. American Cancer Society guidelines for the early detection of cancer: update of early detection guidelines for prostate, colorectal, and endometrial cancers. Also: update 2001--testing for early lung cancer detection. CA: A Cancer Journal for Clinicians. 2001;51(1):38–75. doi: 10.3322/canjclin.51.1.38. quiz 77-80. [DOI] [PubMed] [Google Scholar]
- 22.U.S. Preventive Services Task Force Screening for colorectal cancer: recommendation and rationale. Annals of Internal Medicine. 2002;137(2):129–31. doi: 10.7326/0003-4819-137-2-200207160-00014. [DOI] [PubMed] [Google Scholar]
- 23.Winawer S, Fletcher R, Rex D, Bond J, Burt R, Ferrucci J, et al. Colorectal cancer screening and surveillance: clinical guidelines and rationale-Update based on new evidence. Gastroenterology. 2003;124(2):544–60. doi: 10.1053/gast.2003.50044. [DOI] [PubMed] [Google Scholar]
- 24.Smith RA, Cokkinides V, Brawley OW. Cancer screening in the United States, 2009: A review of current American Cancer Society guidelines and issues in cancer screening. CA A Cancer Journal for Clinicians. 2009;59(1):27–41. doi: 10.3322/caac.20008. [DOI] [PubMed] [Google Scholar]
- 25.Subramanian S, Klosterman M, Amonkar MM, Hunt TL. Adherence with colorectal cancer screening guidelines: a review. Preventive Medicine. 2004;38(5):536–50. doi: 10.1016/j.ypmed.2003.12.011. [DOI] [PubMed] [Google Scholar]
- 26.Vernon SW. Participation in colorectal cancer screening: a review. J. Natl. Cancer Inst. 1997;89(19):1406–1422. doi: 10.1093/jnci/89.19.1406. [DOI] [PubMed] [Google Scholar]
- 27.Blalock SJ, DeVellis BM, Sandler RS. Participation in fecal occult blood screening: a critical review. Preventive Medicine. 1987;16(1):9–18. doi: 10.1016/0091-7435(87)90002-8. [DOI] [PubMed] [Google Scholar]
- 28.Glanz K, Rimer BK, Lewis FM. Health Behavior and Health Education: Theory, Research and Practice. 4rd ed. Jossey-Bass; San Francisco, CA: 2008. [Google Scholar]
- 29.Salovey P, Rothman AJ, Rodin J. Health behavior. In: Gilbert DT, Fiske ST, Lindzey G, editors. The handbook of social psychology. 4 ed McGraw-Hill; 1998. pp. 633–683. [Google Scholar]
- 30.Weinstein ND. Testing four competing theories of health-protective behavior. Health Psychology. 1993;12(4):324–333. doi: 10.1037//0278-6133.12.4.324. [DOI] [PubMed] [Google Scholar]
- 31.D'Onofrio CN. Theory and the empowerment of health education practitioners. Health Education Quarterly. 1992;19(3):385–403. doi: 10.1177/109019819201900309. [DOI] [PubMed] [Google Scholar]
- 32.Rothman AJ, Salovey P. The Reciprocal Relation between Principles and Practice: Social Psychology and Health Behavior. In: Kruglanski AW, Higgins ET, editors. Social Psychology: Handbook of Basic Principles. 2nd ed. Guilford; New York: 2007. pp. 826–849. [Google Scholar]
- 33.Baranowski T. Advances in basic behavioral research will make the most important contributions to effective dietary change programs at this time. J Am Diet Assoc. 2006;106(6):808–11. doi: 10.1016/j.jada.2006.03.032. [DOI] [PubMed] [Google Scholar]
- 34.Rosenstock IM. Historical origins of the health belief model. Health Education Monographs. 1974;2:1–8. doi: 10.1177/109019817800600406. [DOI] [PubMed] [Google Scholar]
- 35.Ajzen I. The theory of planned behavior. Organizational Behavior and Human Decision Processes. 1991;50(2):179–211. [Google Scholar]
- 36.Bandura A. Social foundations of thought and action: A social cognitive theory. Prentice-Hall, Inc; Englewood Cliffs, NJ, US: 1986. [Google Scholar]
- 37.Prochaska JO, DiClemente CC, Norcross JC. In search of how people change: Applications to addictive behaviors. American Psychologist. 1992;47(9):1102–1114. doi: 10.1037//0003-066x.47.9.1102. [DOI] [PubMed] [Google Scholar]
- 38.Noar SM, Zimmerman RS. Health Behavior Theory and cumulative knowledge regarding health behaviors: are we moving in the right direction? 2005;20(3):275–290. doi: 10.1093/her/cyg113. [DOI] [PubMed] [Google Scholar]
- 39.Cohen J. A Power Primer. Psychological Bulletin. 1992;112(1):155–159. doi: 10.1037//0033-2909.112.1.155. [DOI] [PubMed] [Google Scholar]
- 40.McKenzie JF, Neiger B,L, Smeltzer JL. 4th ed. Pearson; San Francisco: 2005. Planning, implementing, and evaluating health promotion programs. [Google Scholar]
- 41.National Cancer Institute . Making health communication programs work. US Department of Health and Human Service; Washington, DC: 2001. [Google Scholar]
- 42.Eagly AH, Chaiken S. The psychology of attitudes. Harcourt Brace Jovanovich; New York: 1993. [Google Scholar]
- 43.Wardle J, Sutton S, Williamson S, Taylor T, McCaffery K, Cuzick J, et al. Psychosocial influences on older adults’ interest in participating in bowel cancer screening. Prev Med. 2000;31(4):323–34. doi: 10.1006/pmed.2000.0725. [DOI] [PubMed] [Google Scholar]
- 44.Yepes-Rios M, Reimann JOF, Talavera AC, Ruiz de Esparza A, Talavera GA. Colorectal cancer screening among Mexican Americans at a community clinic. Am J Prev Med. 2006;30(3):204–10. doi: 10.1016/j.amepre.2005.11.002. [DOI] [PubMed] [Google Scholar]
- 45.Albarracin D, Zanna MP, Johnson BT, Kumkale GT. Attitudes: Introduction and Scope. In: Albarracin D, Johnson BT, Zanna MP, editors. The handbook of attitudes. Lawrence Erlbaum Associates Publishers; Mahwah, NJ US: 2005. pp. 3–19. [Google Scholar]
- 46.Vernon SW, Myers RE, Tilley BC. Development and validation of an instrument to measure factors related to colorectal cancer screening adherence. Cancer Epidemiology, Biomarkers, and Prevention. 1997;6(10):825–832. [PubMed] [Google Scholar]
- 47.Tiro JA, Vernon SW, Hyslop T, Myers RE. Factorial validity and invariance of a survey measuring psychosocial correlates of colorectal cancer screening among African Americans and Caucasians. Cancer Epidemiology Biomarkers & Prevention. 2005;14(12):2855–2861. doi: 10.1158/1055-9965.EPI-05-0217. [DOI] [PubMed] [Google Scholar]
- 48.Klein WM. Objective standards are not enough: Affective, self-evaluative, and behavioral responses to social comparison information. Journal of Personality and Social Psychology. 1997;72(4):763–774. doi: 10.1037//0022-3514.72.4.763. [DOI] [PubMed] [Google Scholar]
- 49.Rawl S, Champion V, Menon U, Loehrer PJ, Vance GH, Skinner CS. Validation of scales to measure benefits of and barriers to colorectal cancer screening. Journal of Psychosocial Oncology. 2001;19(3):47–63. [Google Scholar]
- 50.Vernon SW, Meissner H, Klabunde C, Rimer BK, Ahnen DJ, Bastani R, et al. Measures for ascertaining use of colorectal cancer screening in behavioral, health services, and epidemiologic research. Cancer Epidemiology, Biomarkers, and Prevention. 2004;13(6):898–905. [PubMed] [Google Scholar]
- 51.National Cancer Institute [August 31, 2010];Health Behavior Constructs: Theory, Measurement, and Research. 2008 Available at: http://cancercontrol.cancer.gov/brp/constructs/.
