Abstract
The primary aim of this paper was to explore whether provider’s understanding of patient’s social context is associated with screening uptake, independent of provider’s recommendation. Baseline data were collected in 2004–2005 from a cluster randomized control trial in 12 low-income housing sites. Participants included 695 low-income, multiethnic adults aged 50 years and over who were primarily insured (97%). Provider’s recommendation was significantly associated with current adherence to colorectal cancer (CRC) screening. Provider’s understanding of patient’s social context, as operationalized by how well participants felt that their provider knew (a) their responsibilities at work, home, or school; (b) their worries about health; and (c) them as a person and their values and beliefs, was also significantly associated with current adherence to screening, independent of provider’s recommendation. Participants who reported that their provider knew them well on two or three items were significantly more likely to be current with CRC screening compared to those who reported their provider knew them well on only one or none of the items (odds ratio = 1.56; 95% confidence interval = 1.06, 2.29). Our findings indicate that provider’s understanding of patient’s social context, independent of provider’s recommendation for CRC screening, contributed to adherence to CRC screening in this low-income, multiethnic population.
Keywords: Urban low-income population, Colorectal cancer, Social context, Provider’s recommendation for CRC screening
Introduction
Colorectal cancer (CRC) is the third most common cause of cancer and the second most common cause of cancer death in the USA. Although CRC incidence and mortality rates have been declining, reflecting improvements in early detection and treatment,1 ethnic/racial and socioeconomic disparities still persist. These disparities are due, at least in part, to disparities in CRC screening uptake.2–10
Conceptual Model
This research is guided by the social contextual model put forth by Sorensen et al.,11 which illustrates the role of social contextual factors in influencing health behaviors across multiple levels of influence. Provider’s recommendation for CRC screening has consistently been one of the strongest predictors of CRC screening behavior.12–19 However, the association of screening status and the provider’s understanding of patient’s social context, independent of provider’s recommendation for CRC screening, has not yet been examined. To address this gap, we examined the relative contribution of provider’s understanding of patient’s social context to current CRC screening adherence, independent of receiving a screening recommendation. We hypothesized that participants who had received a recommendation for CRC screening would be more likely to be current with CRC screening than those who had not received a recommendation. We further hypothesized that those who reported that their provider knew their social context well would be more likely to be current with CRC screening than those who reported that their provider did not know their social context well, controlling for provider’s recommendation.
Methods
Study Design and Sample
This study used baseline data collected in 2004–2005 from Open Doors to Health, a CRC prevention cluster randomized control trial. Twelve urban public housing sites in Boston were the primary sampling units, and individuals within housing sites served as secondary sampling units. Participants provided informed consent and completed an interviewer-administered survey in either English or Spanish. The study protocol was approved by the Harvard School of Public Health Institutional Review Board.
Study recruitment and sampling has been described in full detail elsewhere.20 , 21 Eligibility criteria included (1) residence in a participating housing site, (2) at least 18 years of age, and (3) fluency in English or Spanish. Baseline surveys were obtained on 1,554 participants. Analyses included Black, White, and Hispanic participants aged 50 years and over who had completed the baseline survey, including questions pertaining to CRC screening and provider’s understanding of the patient’s social context (n = 695). Due to cognitive or other types of disabilities, 12% of participants completed a shorter version of the survey which did not include these questions. Ninety-seven percent of the overall sample had health insurance that covered CRC screening.
Measures
Provider’s recommendation for CRC was assessed by asking participants whether a health provider ever told them that they should be screened for colon or rectal cancer (yes/no). Participants reported on their regular provider’s understanding of their social context, operationalized as how well they felt their regular provider knew (a) their responsibilities at work, home, or school; (b) their worries about health; and (c) them as a person and their values and beliefs.11 , 22 Responses included not at all, a little, somewhat, and very well for each item. A point was given for each question for which the participants felt their provider knew their social context somewhat or very well, and a summary score (range, 0 to 3) was computed. A median split of two categories was then created (zero to one item = did not know patient’s social context well; two to three items = knew patient’s social context well) for these analyses, based on the distribution of responses. Sociodemographic variables including age, race, gender, income, education, immigrant status, English as a first language, and number of doctor visits in the last year were also assessed. The outcome variable was CRC screening adherence.23 Patients were considered current if they reported having a fecal occult blood test (FOBT) within 1 year of the survey, flexible sigmoidoscopy within 5 years, and/or colonoscopy within 10 years, as per American Cancer Association Screening guidelines.24
Data Analysis
Based on the cluster design, data for all analyses were weighted up to the population size within each housing site (weighted sample size = 1,029). Based on the bivariate associations and consideration of potential confounders, cluster randomized multivariable logistic regression models were estimated for the dependent variable, using SUDAAN 9.01 and SAS 9.1 statistical software.25
Results
Sociodemographic Analyses
Table 1 presents the demographics for the sample. Participants were predominately non-White, female, insured, and had low levels of education.
Table 1.
Demographic characteristics of study sample (weighted N = 1,029)
| Age, mean (SE) | 63.39 (0.31) |
| Race/ethnicity, n (%) | |
| Black | 488 (47) |
| White | 58 (6) |
| Hispanic | 483 (47) |
| Gender, n (%) | |
| Male | 296 (29) |
| Female | 733 (71) |
| Income, n (%) | |
| <$10,000 | 503 (53) |
| $10,000 to <20,000 | 311 (32) |
| >+$20,000 | 137 (14) |
| Education, n (%) | |
| Less than high school | 592 (58) |
| Completed high school/vocational | 220 (21) |
| At least some college | 214 (21) |
| Immigrant status, n (%) | |
| Born in USA | 487 (47) |
| Born in Puerto Rico | 344 (33) |
| Not born in USA or Puerto Rico | 197 (19) |
| English as first language, n (%) | |
| Yes | 521 (51) |
| No | 508 (49) |
| Provider’s understanding of patient’s social context, n (%) | |
| Provider knows patient’s social context somewhat or very well on 0 to 1 item | 307 (30) |
| Provider knows patient’s social context somewhat or very well on 2 to 3 items | 715 (70) |
| Provider’s recommendation for CRC screening, n (%) | |
| Yes | 716 (70) |
| No | 304 (30) |
| Average number of doctor visits/last year, n (SE) | 7 (0.47) |
| Insurance type, n (%) | |
| Public (Medicare, Medicaid, MassHealth) | 783 (77) |
| Public and private | 32 (3) |
| Private only | 183 (18) |
| No insurance | 25 (2) |
| Type of screening, n (%) | |
| Colonoscopy | 557 (54) |
| Flexible sigmoidoscopy | 64 (6) |
| FOBT | 78 (8) |
| Current screening, n (%) | |
| Yes | 699 (67) |
| No | 330 (32) |
Bivariate and Multivariable Analyses for Current CRC Screening
Table 2 presents the bivariate analyses. Participants who had received a recommendation were significantly more likely to be current with their CRC screening compared to those who did not receive one (p = 0.001). Similarly, participants who reported that their provider knew their social context well were significantly more likely to be current with CRC screening compared to those who reported that their provider did not know their social context well (p = 0.004).
Table 2.
Bivariate model predicting current CRC screening
| Bivariate analyses, OR (95% CI) | |
|---|---|
| Demographics | |
| Age | 1.03 (1.01, 1.05)** |
| Race | |
| Hispanic | 1.28 (0.60, 2.74) |
| Black | 1.47 (0.69, 3.13) |
| White | Ref |
| Gender | |
| Male | 1.02 (0.72, 1.44) |
| Female | Ref |
| Income | |
| <$10,000 | 1.30 (0.81, 2.09) |
| $10,000 to <20,000 | 1.26 (0.76,2.09) |
| >+$20,000 | Ref |
| Education | |
| Less than high school | 1.29 (0.86, 1.95) |
| Completed high school/vocational | 0.84 (0.52, 1.35) |
| At least some college | Ref |
| Immigrant status | |
| Born in USA | 1.08 (0.71, 1.64) |
| Born in Puerto Rico | 0.91 (0.57, 1.44) |
| Not born in USA or Puerto Rico | Ref |
| English as first language | |
| Yes | 1.11 (0.81, 1.54) |
| No | Ref |
| Number of doctor visits/last year | 1.73 (1.38, 2.17)* |
| Provider’s recommendation for CRC screening | |
| Yes | 4.63 (3.24, 6.60)** |
| No | Ref |
| Provider’s understanding of patient’s social context | |
| Provider knows patient’s social context somewhat or very well on 0 to 1 item | Ref |
| Provider knows patient’s social context somewhat or very well on 2 to 3 items | 1.79 (1.26, 2.55)** |
*p < 0.05; **p < 0.01
Table 3 displays the odds ratios and 95% confidence intervals for the adjusted multivariable model of current CRC screening. After adjusting for potential confounding factors, the association between receiving a recommendation and being screened remained significant (p = 0.001). The association between provider’s understanding of patient’s social context and current CRC screening also remained significant after adjusting for age, number of times visited the doctor per year, and provider’s recommendation.
Table 3.
Multivariable model predicting current CRC screening
| Multivariable analysesa, OR (95% CI) | |
|---|---|
| Demographics | |
| Age | 1.03 (1.01, 1.05)** |
| Race | |
| Hispanic | |
| Black | |
| White | |
| Gender | |
| Male | |
| Female | |
| Income | |
| <$10,000 | |
| $10,000 to <20,000 | |
| >+$20,000 | |
| Education | |
| Less than high school | |
| Completed high school/vocational | |
| At least some college | |
| Immigrant status | |
| Born in USA | |
| Born in Puerto Rico | |
| Not born in USA or Puerto Rico | |
| English as first language | |
| Yes | |
| No | |
| Number of doctor visits/last year | 1.03 (1.00, 1.05)* |
| Provider’s recommendation for CRC screening | |
| Yes | 4.50 (3.11, 6.52)** |
| No | Ref |
| Provider’s understanding of patient’s social context | |
| Provider knows patient’s social context somewhat or very well on 0 to 1 item | Ref |
| Provider knows patient’s social context somewhat or very well on 2 to 3 items | 1.56 (1.06, 2.29)* |
*p < 0.05; **p < 0.01
aAdjusted for age, number of doctor visits/last year, and provider’s recommendation for CRC screening
Discussion
The aim of this article was to examine whether the provider’s understanding of the patient’s social context was associated with current CRC screening, independent of receiving a recommendation to be screened among a sample of low-income, multiethnic adults. Consistent with previous findings,12–19 provider’s recommendation emerged as a strong predictor of CRC screening. Additionally, as hypothesized, provider’s understanding of patient’s social context was significantly associated with CRC screening, independent of recommendation.
Several limitations must be noted. Participants were asked about screening recommendations made by any health care provider, while provider’s understanding of patient’s social context was assessed specifically for one’s regular provider. Although we considered restricting the recommendation question to the current regular provider, it is possible that another provider would make a CRC screening recommendation (e.g., a nurse at a blood pressure clinic), which would cue the patient to talk with their regular provider about screening. Currently, in most states, CRC screening requires a referral from one’s primary care provider. Thus, it is likely that there was high convergence between the referent for the provider and screening questions. This study is also cross-sectional, and thus, causal interpretations cannot be made. The results can only be generalized to similar populations. Of note, likely because of the high level of health insurance coverage among this sample of public housing residents, access to health care was not generally a barrier and thus may have impacted on the study findings. However, this is an ideal situation in which to study the association between provider’s understanding of patient’s social context and health care utilization because the results are less likely to be influenced by issues of access.
Our findings indicate that provider’s understanding of their patients’ social context may facilitate screening adherence. Although longitudinal data would be needed to assess any causal patterns, it is possible that providers who know their patients better are more effective at participating in the shared decision making that is an important part of addressing cancer screening. These providers may also be more effective at removing barriers to screening because they have a better understanding of their patients’ social context. Thus, our findings are useful in emphasizing important aspects of patients’ social context to which providers need to attend to in their clinical encounters in order to increase CRC screening.
Acknowledgments
We would like to profoundly thank the coinvestigators of this study: Gary Bennett, Sapna Syngal, Robert Mayer, and Martha Zorn. We also gratefully acknowledge the efforts of the Open Doors to Health Research Team: Elise Dietrich, Elizabeth Gonzalez Suarez, Terri Greene, Lucia Leone, Mike Massagli, Vanessa Melamede, Maribel Melendez, Tamara Parent, Lina Rincón, Claudia Viega, Monifa Watson, Caitlin Gutheil, Zoe Bendixen, Roona Ray, Aidana Baldassrre, David Wilson, and Ruth Lederman. Finally, we would also like to thank the resident helpers and resident service coordinators at collaborating housing sites.
This research was supported by grants 5R01CA098864-02, 1K22CA126992-01, and K05 CA124415 from the National Cancer Institute and support to the Dana-Farber Cancer Institute by Liberty Mutual, National Grid, the Patterson Fellowship, and the Yerby Fellowship Program.
References
- 1.Centers for Disease Control and Prevention. Colorectal cancer screening guidelines. Available at: http://www.cdc.gov/cancer/colorectal/basic_info/screening/guidelines.htm. Accessed on: June 17, 2009.
- 2.Shokar NK, Carlson CA, Weller SC. Factors associated with racial/ethnic differences in colorectal cancer screening. J Am Board Fam Med. 2008;21(5):414–426. doi: 10.3122/jabfm.2008.05.070266. [DOI] [PubMed] [Google Scholar]
- 3.Meissner H, Breen N, Klabunde C, Vernon S. Patterns of colorectal cancer screening uptake among men and women in the United States. Cancer Epidemiol Biomarkers Prev. 2006;15:389–394. doi: 10.1158/1055-9965.EPI-05-0678. [DOI] [PubMed] [Google Scholar]
- 4.Seeff LC, Nadel MR, Klabunde CN, et al. Patterns and predictors of colorectal cancer test use in the adult US population. Cancer. 2004;100:2093–2103. doi: 10.1002/cncr.20276. [DOI] [PubMed] [Google Scholar]
- 5.Swan J, Breen N, Coates R, Rimer B, Lee N. Progress in cancer screening practices in the United States: results from the 2000 National Health Interview Survey. Cancer. 2003;97:1528–1540. doi: 10.1002/cncr.11208. [DOI] [PubMed] [Google Scholar]
- 6.Walsh J, Posner S, Perez-Stable E. Colon cancer screening in the ambulatory setting. Prev Med. 2002;35:209–218. doi: 10.1006/pmed.2002.1059. [DOI] [PubMed] [Google Scholar]
- 7.Ananthakrishnan A, Schellhase K, Sparapani R, Laud P, Nuener J. Disparities in colon cancer screening in the Medicare population. Arch Intern Med. 2007;167:258–264. doi: 10.1001/archinte.167.3.258. [DOI] [PubMed] [Google Scholar]
- 8.Lafata JE, Williams LK, Ben-Menachem T, Moon C, Divine G. Colorectal carcinoma screening procedure use among primary care patients. Cancer. 2005;104:1356–1361. doi: 10.1002/cncr.21333. [DOI] [PubMed] [Google Scholar]
- 9.O’Malley A, Forrest C, Feng S, Mandelblatt J. Disparities despite coverage: gaps in colorectal cancer screening among Medicare beneficiaries. Arch Intern Med. 2005;165:2129–2135. doi: 10.1001/archinte.165.18.2129. [DOI] [PubMed] [Google Scholar]
- 10.Wee C, McCarthy E, Phillips R. Factors associated with colon cancer screening: the role of patient factors and physician counseling. Prev Med. 2005;41:23–29. doi: 10.1016/j.ypmed.2004.11.004. [DOI] [PubMed] [Google Scholar]
- 11.Sorensen G, Emmons K, Hunt MK, et al. Model for incorporating social context in health behavior interventions: applications for cancer prevention for working-class, multiethnic populations. Prev Med. 2003;37(3):188–197. doi: 10.1016/S0091-7435(03)00111-7. [DOI] [PubMed] [Google Scholar]
- 12.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]
- 13.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]
- 14.Ruchlin HS. Prevalence and correlates of breast and cervical cancer screening among older women. Obstet Gynecol. 1997;90:16–21. doi: 10.1016/S0029-7844(97)00220-2. [DOI] [PubMed] [Google Scholar]
- 15.Beydoun HA, Beydoun MA. Predictors of colorectal cancer screening behaviors among average-risk older adults in the United States. Cancer Causes Control. 2008;19(4):339–359. doi: 10.1007/s10552-007-9100-y. [DOI] [PubMed] [Google Scholar]
- 16.Gilbert A, Kanarek N. Colorectal cancer screening: physician recommendation is influential advice to Marylanders. Prev Med. 2005;41(2):367–379. doi: 10.1016/j.ypmed.2005.01.008. [DOI] [PubMed] [Google Scholar]
- 17.Honda K. Factors associated with colorectal cancer screening among the US urban Japanese population. Am J Public Health. 2004;94(5):815–822. doi: 10.2105/AJPH.94.5.815. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Hay JL, Ford JS, Klein D, et al. Adherence to colorectal cancer screening in mammography-adherent older women. J Behav Med. 2003;26(6):553–576. doi: 10.1023/A:1026253802962. [DOI] [PubMed] [Google Scholar]
- 19.Janz NK, Wren PA, Schottenfeld D, Guire KE. Colorectal cancer screening attitudes and behavior: a population-based study. Prev Med. 2003;37(6 Pt 1):627–634. doi: 10.1016/j.ypmed.2003.09.016. [DOI] [PubMed] [Google Scholar]
- 20.Bennett GG, McNeill LH, Wolin KY, Duncan DT, Puleo E, Emmons KM. Safe to walk? Neighborhood safety and physical activity among public housing residents. PLoS Med. 2007;4(10):1599–1606. doi: 10.1371/journal.pmed.0040306. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.McNeill LH, Puleo E, Bennett GG, Emmons KM. Exploring social contextual correlates of computer ownership and frequency of use among urban, low-income, public housing adult residents. J Med Internet Res. 2007;9(4):e35. doi: 10.2196/jmir.9.4.e35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Zapka J. Colorectal Screening Participation. NIH-funded grant; 2001.
- 23.Vernon SW, Meissner H, Klabunde C, et al. Measures for ascertaining use of colorectal cancer screening in behavioral, health service, and epidemiologic research. Cancer Epidemiol Biomarkers Prev. 2004;13(6):898–905. [PubMed] [Google Scholar]
- 24.American Cancer Society. Guidelines for early detection of cancer, 2006, Available at: http://www.cancer.org/docroot/PED/content/PED_2_3X_ACS_Cancer_Detection_Guidelines_36.asp. Accessed on: June 2, 2009.
- 25.Stokes ME, Davis CS, Koch GG. Categorical Data Analysis Using the SAS System. Cary: SAS Institute; 2000. [Google Scholar]
