Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2024 Dec 1.
Published in final edited form as: J Cancer Educ. 2023 Jul 13;38(6):1816–1824. doi: 10.1007/s13187-023-02337-1

Association of preventive care attitudes and beliefs with colorectal cancer screening history among African American patients of community health centers

John S Luque 1, Gebre-Egziabher Kiros 2, Matthew Vargas 3, Deloria R Jackson 4, Olayemi O Matthew 5, Tifini D Austin 6, Rima Tawk 7, Askal A Ali 8, Cynthia M Harris 9, Kristin Wallace 10, Clement K Gwede 11
PMCID: PMC10787027  NIHMSID: NIHMS1938368  PMID: 37442915

Abstract

Colorectal cancer (CRC) is the third most common cancer and third leading cause of cancer-related death among African Americans in the United States. However, when detected early, CRC is treatable and survival rates are high. CRC health disparities for African Americans compared with other groups may be due in part to lower screening adherence and later stage diagnosis. The objective of this research phase was to test predictors of ever having received CRC screening (i.e., self-report of lifetime receipt of CRC screening) using survey measures in the domains of healthcare communication, trust in doctors, CRC perceived susceptibility, CRC worry, negative cancer beliefs, CRC screening self-efficacy, and cultural constructs for CRC screening in a sample of African American community health center patients. The study recruited 115 African American patients between the ages of 45 to 64 years old from community health centers in north Florida to complete the baseline survey. Our results show significant differences in CRC screening history by age, marital status, level of mistrust of healthcare providers, and level of empowerment toward cancer screening. To increase CRC screening in this population, the study findings suggest development of intervention programs that focus on priority populations of younger, unmarried African Americans, especially given the current trend of early onset CRC. Moreover, survival rates are lower for unmarried and younger African Americans relative to older and married individuals. Such interventions should also aim to increase trust in healthcare providers and increase empowerment for CRC screening decision making to increase screening participation.

Keywords: Colorectal cancer, Cancer screening, African Americans, Survey research

Introduction

Colorectal cancer (CRC) is the third most common cancer and third leading cause of cancer-related death among African Americans. African Americans had 40% higher mortality rates for men and 30% higher mortality rates for women compared to non-Hispanic whites (2014-18) for CRC [1]. Cancer health disparities in mortality for African Americans have been attributed to lower rates of screening and lower stage-specific survival rates [2]. CRC screening rates for African Americans are also lower than their white counterparts. The target for Healthy People 2030 is for 68.3% of the age-eligible population to receive CRC screening based on the most recent guidelines [3]. In Florida, 69.3% of whites compared to 53.1% of African Americans had received a colonoscopy in the past 10 years (2018), and 17.6% of whites compared to 26.4% of African Americans had received a stool-based test in the last year (2020) [4]. These numbers for Florida suggest there may be greater barriers for access to colonoscopy that may explain the lower screening rates for African Americans for the most common screening test.

For CRC screening, an analysis of data from the National Health Interview Survey (NHIS) reported that between 2019 and 2021, CRC screening slightly decreased for men from 46.4% to 45.5% and slightly increased for women from 40.6% to 41.6% [5]. The past-year stool blood test rate increased from 7.0% to 10.3% but past-year colonoscopy use decreased from 15.5% to 13.8% [5]. The uptick in stool-based CRC screening is partly an artifact of screening trends during the Covid-19 pandemic, during which time there were fewer colonoscopy procedures [5]. Consequently, there has been a trend toward increased use of stool-based tests, which is a front-line test used in community health centers across the US [6]. Stool-based screening across community health centers (CHC) in the US averaged 44% in 2020, so there is potential for improvement [7]. Barriers for CHCs to improve CRC screening rates include lack of in-facility testing, knowledge and attitudes toward CRC screening, and barriers with implementing effective intervention strategies such as using patient navigators and leveraging electronic medical record systems more effectively [7].

When detected at an earlier stage of disease, CRC is treatable and survival rates are high. However, early detection is a function of CRC screening adherence. Average-risk persons in the US are adherent if they have received a colonoscopy within the last 10 years or a stool blood test within the last year [e.g., fecal immunochemical test (FIT) or a stool DNA test within the last 3 years]. A provider may recommend additional testing to look for cancer or polyps in the colon following a positive stool test. During a colonoscopy screening when the patient is sedated, precancerous polyps can be removed during the procedure to prevent CRC. An assessment of the magnitude of perceived net benefits issued by the US Preventive Services Task Force (USPSTF) provides a “B” recommendation for all average-risk persons to participate in CRC screening between the ages of 45 to 49 years, and an “A” recommendation for adults between the ages of 50 and 75 years [3].

The Test Up Now Education Program (TUNE-UP) study recruited research participants based on not being adherent with CRC screening, and adherence was determined as 9 years since last colonoscopy (10-year screening interval recommended) or 9 months since last stool blood test (1-year screening interval recommended for the FIT). The objective of this research phase was to test baseline predictors of ever having received CRC screening (i.e., self-report of lifetime receipt of any recommended CRC screening) using survey measures in the domains of healthcare communication, trust in doctors, CRC perceived susceptibility, CRC worry, negative cancer beliefs, CRC screening self-efficacy, and cultural constructs for CRC screening in a sample of African American community health center patients who met eligibility requirements to be enrolled in the study.

Methods

The TUNE-UP study is a two-group pretest/posttest pragmatic randomized behavioral clinical trial (Clinical trial registration: NCT04304001). The primary study aim is to test the effectiveness of a community health advisor intervention to increase stool-based testing for CRC. The intervention and the study protocol for the trial have been published elsewhere [8, 9]. The study was approved by the Florida A&M University Institutional Review Board (IRB#1439452-2).

Data collection and study measures

The baseline survey questions were drawn from the Health Information National Trends Survey (HINTS) on demographics, body mass index (BMI), insurance coverage, having a regular healthcare provider, history of tobacco use, self-reported health status, current chronic health condition, feelings of depression or anxiety, family history of cancer, and beliefs and worry about getting cancer and seeking care [10]. In addition, there were validated scales or single items on health literacy [11], healthcare communication [10], trust in doctors [12], CRC perceived susceptibility [13], CRC worry [14], negative cancer beliefs [10], CRC screening self-efficacy [13], depression (PHQ-2) [15], generalized anxiety disorder (GAD-2) [16], and cultural factors related to cancer screening from the multi-construct African American Cultural Survey (MAACS) [17]. The binary dependent variable assessed whether participants had ever received CRC screening [14].

Participant recruitment and study eligibility

To be eligible for the study, study participants needed to satisfy specific inclusion criteria: (1) 45-64 years old, (2) African American, (3) working phone, (4) Florida resident, (5) not be up-to-date to screening (>9 months since stool test, >9 years since last colonoscopy, or >4 years since last flexible sigmoidoscopy), and (6) be a patient of one of two community health centers (CHC) in the study area in north Florida. Participants were excluded during the informed consent process if they had a previous history of CRC, precancerous polyps, or certain health conditions such as Lynch syndrome, Crohn’s disease, or diseases of the bowels. With the assistance of the two CHC’s, bimonthly text messages were sent to CHC patients with instructions to contact the project coordinator to determine study eligibility if they expressed interest. There was also a recruitment flyer with the project coordinator’s contact information posted in the CHC waiting room areas as well as community events where the CHC was a partner. Participant recruitment began in April 2021 and lasted through March 2023. The project coordinator determined eligibility over the phone, administered the verbal informed consent, and met with the study participants to administer the baseline survey face-to-face. Participants received a copy of the consent form, completed the gift card receipt form, and received a $20 retail store gift card as compensation for their participation. They also received a tailored educational brochure titled, What Black Men and Women need to know about Colorectal Cancer Screening [18].

Data management

Participants were all assigned a unique identification number. The paper surveys were double entered into the REDCap research management software platform by two research assistants to ensure accuracy. REDCap is a secure web application hosted on a local server to facilitate the management of survey data and enable export to statistical packages for analysis [19].

Statistical analysis

All statistical analyses were conducted using SAS v. 9.4. First, descriptive statistics were generated for all variables. Next, bivariate analyses were performed for key variables to compare differences on the dichotomous variable, “ever received CRC screening.” Categorical variables were compared using chi-square tests, and continuous variables, including scale variables, were compared using two-sample t-tests. The predictors that were found to be related to CRC screening history (1=yes; 2=no) in the bivariate analysis (p<0.10) were then entered into a multivariate logistic regression model.

Results

Over the two-year recruitment period for the TUNE-UP clinical trial, 115 participants completed the baseline survey. Over half of the participants (55%) were female and less than half (45%) were male. Close to two-thirds of participants (64%) had a regular health care provider, and 76% of participants reported that this provider was their medical home. Over half of participants (60%) had some form of health insurance such as Medicaid (21%), an individual plan (e.g., ACA Marketplace), (16%), or an employer-based health insurance plan (5%). One-third of participants (33%) were employed. Survey participants had a mean age of 54.7 years (standard deviation = 5.4) and 23% were married or living with a partner. In response to the question if a doctor had discussed different CRC screening tests, 57% of participants responded “yes.” Over one-third of participants (37%) reported fair or poor health status; however, the vast majority (95%) reported some type of chronic health condition (e.g., diabetes or high blood pressure). In response to the question of whether participants had ever received CRC screening, 32% responded “yes.” For those who responded “no,” reasons included “I am going to discuss with my doctor,” “I am planning to be screened next year,” and “never heard of the tests.” Table 1 provides additional details on the results of the chi-square tests organized by the dependent variable, “ever completed CRC screening.”

Table 1.

Sociodemographic Characteristics and Cancer Perceptions of African Americans by Ever Screened Status for Colorectal Cancer

Characteristics Total
(n)a
CRC Screening
Ever (yes), %
CRC Screening
Ever (no), %
p values
Overall 115 32.2 67.8 <.001
Age group (years)
 45-54 54 31.4 59.7 .006
 55-64 53 68.6 40.3
Gender
 Male 52 38.5 61.5 .190
 Female 63 27.0 73.0
Marital status
 Single/separated/widowed/divorced 89 29.2 70.8 .209
 Married/living with a partner 26 42.3 57.7
Education
 <11 years 16 31.3 68.8 .207
 12 years or high school 37 21.6 78.4
 Some college, technical, or higher 59 39.0 61.0
Employed
 Yes 38 23.7 76.3 .171
 No 77 36.4 63.6
BMI
 Normal weight, 18.5-24.9 15 26.7 73.3 .402
 Overweight, 20.0-29.9 28 25.0 75.0
 Obese, ≥30.0 63 38.1 61.9
Health insurance coverage
 Yes 46 33.3 66.7 .744
 No 69 30.4 69.6
Have a regular provider
 Yes 74 33.8 66.2 .620
 No 41 29.3 70.7
History of smoking cigarettes
 Yes 53 34.0 66.0 .749
 No 61 31.1 68.9
Self-reported health status
 Excellent/very good 29 48.3 51.7 .123
 Good 42 26.2 73.9
 Fair/poor 41 29.3 70.7
Current chronic health conditionb
 Yes 96 32.3 67.7 .661
 No 5 40.0 60.0
Depression or anxiety
 Yes 39 38.5 28.6 .289
 No 70 61.5 71.4
Family history of cancer
 Yes 73 30.1 69.9 .425
 No 40 37.5 62.5
Chances of getting cancer
 Very unlikely/unlikely 30 36.7 63.3 .634
 Neither unlikely nor likely 46 28.3 71.7
 Very likely/likely 35 37.1 62.9
Worry about cancer
 Not at all/slightly 48 41.7 58.3 .084
 Somewhat 25 16.0 84.0
 Moderately/extremely 41 31.7 68.3
If you were diagnosed with cancer, obtaining follow-up care would be difficult
 Yes 28 28.6 71.4 .724
 No 84 32.1 67.9
a

Total may not sum to 115 for some questions because of missing data.

b

Derived variable from five different types of chronic conditions, including diabetes, high blood pressure, heart conditions, chronic lung disease (or asthma, emphysema, chronic bronchitis), and arthritis or rheumatism.

Bivariate analysis of scale measures for cancer-related beliefs and attitudes were also conducted to test for differences. For participants who had never been screened, there were more overall negative responses to having had positive healthcare communication with their providers, indicated by a higher mean score on the 7-item scale, but it did not reach statistical significance (p = .08). For participants who had never been screened, there was a higher level of disagreement regarding having trust in their physician (p = .04). For participants who had never received CRC screening there was a lower level of CRC worry, but it was not statistically significant (p = .06). For the other scale measures, there were no statistically significant differences between the groups based on the dependent variable of screening receipt, except for the MAACS subscale on empowerment which indicated higher scores for those in category of ever being screened, indicating greater empowerment around personal agency and cancer screening on the 6-item subscale (p = .03). Table 2 provides additional details on the results of the t-tests with values organized by the dependent variable, “ever completed CRC screening.”

Table 2.

Responses for Cancer-Related Beliefs and Attitudes by Ever Screened Status for Colorectal Cancer

Characteristics CRC Screening Ever
(yes) (M ± SD)
CRC Screening Ever
(no) (M ± SD)
p
values
Health Literacy Screener a
 How often do you have difficulty learning about your health or medical condition due to not understanding what is written? 1.62 ± 0.68 1.59 ± 0.63 .806
Healthcare Communication Scale b 9.59 ± 4.90 11.63 ± 5.40 .075
 How often did they give you the chance to ask all the health-related questions you had?
 How often did they give you the attention you needed to your feelings and emotions?
 How often did they involve you in decisions about your health care as much as you wanted?
 How often did they make sure you understood the things you needed to do to take care of your health?
 How often did they explain things in a way you could understand?
 How often did they spend enough time with you?
 How often did they help you deal with feelings of uncertainty about your health or health care?
Trust in Doctors Scale c 19.41 ± 6.33 22.22 ± 7.16 .044*
 Your doctor does whatever it takes to get you the care you need
 Sometimes your doctor cares more about convenience than your health care
 Your doctor’s medical skills are not as good as they should be
 Your doctor is extremely thorough and careful
 You completely trust your doctor’s decisions about what’s best for you
 Your doctor is totally honest about all treatment options available to you
 Your doctor only thinks about what is best for you
 Sometimes your doctor doesn’t pay full attention to what you’re telling them
 You have no worries about putting your life in your doctor’s hands
 You completely trust your doctor
CRC perceived susceptibility d 8.78 ± 1.89 9.03 ± 2.23 .570
 I believe the chance I might develop CRC is high
 I think it is very likely I will develop CRC or polyps
 I believe the chance I will develop colorectal polyps is high
CRC worry d 6.41 ± 1.28 5.85 ± 1.53 .057
 I am afraid of having an abnormal screening result
 I am worried that screening will show that I have CRC or polyps
Negative cancer beliefs d 10.68 ± 2.03 10.44 ± 2.56 .618
 It seems like everything causes cancer
 There’s not much you can do to lower your chances of getting cancer
 It’s so hard to know which cancer prevention recommendations to follow
 In adults, cancer is more common than heart disease
CRC screening self-efficacy d 7.59 ± 2.14 7.92 ± 2.21 .453
 Arranging my schedule for CRC screening is easy
 Finding time for CRC screening would be difficult
 Going through CRC screening would be difficult
 Going through CRC screening would be easy
Patient Health Questionnaire 2-item (PHQ-2) e 1.89 ± 1.88 1.88 ± 1.85 .988
 Over the past 2 weeks how often have you been bothered by having little interest in doing things?
 Feeling down/depressed/hopeless?
Generalized Anxiety Disorder 2-item (GAD-2) e 1.81 ± 2.07 1.62 ± 1.92 .643
 Feeling nervous/anxious/on edge?
 Not able to stop/control worrying?
MAACS Measures and Subscales f
 MAACS Religiosity (6 items) 24.35 ± 3.56 24.40 ± 4.66 .958
 MAACS Mistrust/Discrimination (9 items) 25.97 ± 4.94 25.19 ± 4.42 .396
 MAACS Privacy (6 items) 14.11 ± 5.41 14.94 ± 4.39 .383
 MAACS Ethnic Identity (7 items) 24.58 ± 5.37 24.01 ± 4.38 .557
 MAACS Collectivism (5 items) 18.65 ± 3.85 17.38 ± 4.21 .125
 MAACS Empowerment (6 items) 24.95 ± 3.52 23.13 ± 4.40 .030*
 MAACS Male Role (4 items) 14.38 ± 3.51 15.05 ± 3.41 .330

Note: Values in bold represent summary scale scores.

a

Response categories for this item is the following: 1 = never; 2 = sometimes; 3 = always.

b

Only participants who had a regular provider answered these questions. Response categories for these items are the following: 1 = always; 2 = usually; 3 = sometimes; 4 = never.

c

Response categories for these items are the following: 1 = strongly agree; 2 = agree; 3 = neutral; 4 = disagree; 5 = strongly disagree.

d

Response categories for these items are the following: 1 = strongly agree; 2 = agree; 3 = disagree; 4 = strongly disagree.

e

Response categories for these items are the following: 0 = not at all; 1 = several days; 2 = more than half the days; 3 = nearly every day.

f

Response categories for these items are the following: 1 = strongly disagree; 2 = disagree; 3 = neutral; 4 = agree; 5 = strongly agree.

*

p < 0.05

Table 3 presents odds ratios and their 95% confidence intervals from a multivariate logistic regression model predicting ever having received CRC screening. Three sets of predictors were included in the model: Socio-demographic (gender, age, marital status, education, and employment), Communication/Trust scales (healthcare communication, trust in doctors, and CRC worry), and seven MAACS subscales. The likelihood ratio chi-squared value (35.4, df=15, p < 0.01) showed the logistic model presented fit the data well. From the socio-economic factors considered, age and marital status were significant predictors of CRC screening history. Study participants in the 55-64 age-group were about seven times more likely (OR = 6.58, 95% CI 1.75-24.77) to ever being screened compared to participants in the 45-54 age-group. Participants who were married or living with a partner were about ten times more likely (OR = 10.56, 95% CI 1.73-64.41) to ever being screened relative to those who were single (also included separated, widowed, or divorced individuals). Study participants who had higher levels of education were close to five times more likely (OR = 4.66, 95% CI 1.21-17.91) to ever being screened compared to those with lower levels of education. From the MAACS measures, only mistrust and empowerment were significantly associated with ever having received CRC screening. Higher values on the MAACS mistrust subscale (i.e., greater trust) were positively associated with ever being screened (OR = 1.26, 95% CI 1.01-1.56). In addition, higher values on the MAACS empowerment scale (i.e., more empowerment) were also positively associated with ever being screened (OR = 1.29, 95% CI 1.03-1.61).

Table 3.

Multivariate Logistic Regression Predicting Ever Having Received CRC Screening (N = 115)

Socio-demographic Variables OR 95% CI p values
Gender
 Female REF
 Male 2.28 0.62-8.39 .213
Age Group (years)
 45-54 REF
 55-64 6.58 1.75-24.77 .005*
Marital status
 Single/separated/widowed/divorced REF
 Married/living with a partner 10.56 1.73-64.41 .011*
Education
 <12 years or high school REF
 Some college, technical, or higher 4.66 1.21-17.91 .025*
Employed
 Employed REF
 Not employed 4.42 0.86-22.75 .076
Communication and Trust
 Health Care Communication Scale 0.88 0.73-1.06 .172
 Trust in Doctors Scale 1.01 0.88-1.16 .851
 CRC Worry 1.60 0.98-2.63 .062
MAACSa Measures and Subscales
 MAACS Religiosity 0.86 0.72-1.03 .103
 MAACS Mistrust/Discrimination 1.26 1.01-1.56 .038*
 MAACS Privacy 1.06 0.90-1.26 .496
 MAACS Ethnic Identity 0.97 0.84-1.12 .701
 MAACS Collectivism 0.88 0.69-1.12 .298
 MAACS Empowerment 1.29 1.03-1.61 .028*
 MAACS Male Role 0.87 0.72-1.05 .141
a

Multi-construct African American Cultural Survey

*

p < 0.05

Discussion

The study findings indicate significant differences in CRC screening history by age, marital status, mistrust of healthcare providers, and empowerment toward cancer screening. To increase CRC screening in this African American patient population of CHCs, the results point to the importance of intervention programs to consider priority populations such as younger and single African Americans, especially given the current trend of early onset CRC [20]. This study included individuals in the 45–49-year-old category, a population that should be prioritized for CRC screening, and in this case, utilized stool-based tests in the context of being a patient of a CHC. A separate study with 817 African American patients also identified age as a significant predictor of intention to receive a stool blood test [21]. Moreover, while younger individuals tend to underutilize CRC screening, married individuals have higher rates of adherence. A study using US national survey data reported 69% of married participants completed CRC screening compared to 53% of never married individuals [22]. Our study adds to the literature on the effect of marital status on screening to show that among an African American patient population with a low level of CRC screening, there was a 13-percentage point difference by marital status.

Screening interventions should also aim to increase trust in healthcare providers and increase empowerment for CRC screening decision making. The 6-item empowerment subscale and 9-item mistrust/discrimination subscale from the MAACS were significant predictors of CRC screening history. A prior systematic review reported that medical mistrust is a factor which may partially explain CRC screening disparities in African Americans [23]. This study identifies mistrust/discrimination, which included items regarding preference for an African American doctor, trust in doctors, and racial discrimination in the doctor’s office, as associated with CRC screening history. Like the Thompson et al. study, among the sociocultural variables considered from the MAACS, in our study, empowerment also had the strongest association with CRC screening, and consequently, this cultural construct should be considered when designing intervention programs [17]. Our study adds additional evidence for the importance of empowerment (i.e., strong belief in individual’s ability to affect cancer outcomes) related to CRC screening; however, unlike the Thompson et al. study, our study did not find evidence that participants who held strong privacy beliefs were less like to have participated in CRC screening [17]. To bolster empowerment, intervention materials should reinforce the belief that having regular screening tests will prolong a person’s life, help to support the family, and avoid future medical problems.

Another study with African Americans examined discussions with providers for CRC screening and reported that 48% of 103 African American male participants did not receive a recommendation from their provider for CRC screening [24]. A clinical trial of a computer-based intervention to increase CRC screening identified patient-provider discussions as a mediator for completing a stool blood test [25]. In our study, 57% of participants had discussed CRC screening with their doctor, but only 32% reported ever receiving CRC screening. Provider recommendation for cancer screening is an effective strategy for increasing cancer screening adherence. Thus, providers and the healthcare team have a vital role to play to help inculcate the behavior of regular CRC screening to boost screening rates.

Limitations

There were some limitations to this study. The first limitation is that screening history was based on self-report. Confirmation of CRC screening was not objectively verified by medical record review at baseline. Per study eligibility, all participants were determined not to be up to date with screening based on self-report. Further, the sample size was not large, but it was sufficient to predict screening history based on a limited set of variables selected for the analysis. The study relied on CHC text messaging for recruitment of participants by asking them to contact the study coordinator. Another major challenge in recruiting participants consisted of the fact that 202 potential participants who showed interest in participating were either up to date with CRC screening or were not enrolled because of other exclusion criteria.

Conclusion

Cancer health disparities persist for African Americans, especially in the US South where health insurance rates are lower, partly because many of the southern states have declined to participate in Medicaid expansion under the Affordable Care Act [26]. Consequently, additional studies are needed to examine the individual and structural factors related to CRC screening in African Americans to inform intervention programs. The scales and individual items used in the survey collected reliable data to measure beliefs and attitudes toward CRC screening among African American CHC patients. This study identified key cultural barriers (mistrust/discrimination) and facilitators (empowerment) to CRC screening that merit consideration when designing intervention programs to increase screening. Results of the current study were similar to past research findings that older and married individuals were more likely to have ever received CRC screening. Subsequent study activities include completing the 12-month follow-up surveys with participants and electronic medical record verification of CRC screening to test the effectiveness of the community health advisor educational intervention to increase stool-based screening. The goal of our research program is to decrease CRC screening disparities for African Americans by delivering culturally appropriate intervention and outreach programs.

Acknowledgements

We sincerely appreciate the invaluable assistance of the U54 RCMI Community Engagement Core headed by Dr. Sandra Suther and our community partners from Bond Community Health Center (Dr. Temple O. Robinson, MD, and Ms. Bessie Duncan) and Neighborhood Medical Center (Ms. Jeanne’ S. Freeman, Mr. Mark Leonard, and Ms. Yolanda Gibson) for providing critical assistance with recruiting participants and organizing team meetings. Finally, we acknowledge support of the U54 RCMI Center Office – Ms. Leola Hubert-Randolph and Ms. Gloria O. James–Academic Support Services, Florida A&M University College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health and U54 RCMI Principal Investigator, Dr. Karam F. Soliman.

Funding

This article was supported by funding from the National Institute on Minority Health and Health Disparities of the National Institutes of Health under Award Number U54 MD007582. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Contributor Information

John S. Luque, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Gebre-Egziabher Kiros, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA.

Matthew Vargas, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA.

Deloria R. Jackson, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Olayemi O. Matthew, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Tifini D. Austin, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Rima Tawk, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA.

Askal A. Ali, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Cynthia M. Harris, College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA

Kristin Wallace, Department of Public Health Sciences, College of Medicine, Medical University of South Carolina, 68 President Street, Charleston, SC 29425, USA; Hollings Cancer Center, Medical University of South Carolina, 86 Jonathan Lucas Street, Charleston, SC 29425, USA.

Clement K. Gwede, Division of Population Sciences, Department of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa, FL 33612, USA

References

  • 1.Giaquinto AN, Miller KD, Tossas KY, Winn RA, Jemal A, Siegel RL. 2022. Cancer statistics for African American/Black People 2022. CA: A Cancer Journal for Clinicians. 72(3):202–29. 10.3322/caac.21718. [DOI] [PubMed] [Google Scholar]
  • 2.Lansdorp-Vogelaar I, Kuntz KM, Knudsen AB, van Ballegooijen M, Zauber AG, Jemal A. 2012. Contribution of screening and survival differences to racial disparities in colorectal cancer rates. Cancer Epidemiology, Biomarkers & Prevention. 21(5):728–36. 10.1158/1055-9965.EPI-12-0023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.U. S. Preventive Services Task Force, Davidson KW, Barry MJ, Mangione CM, Cabana M, Caughey AB, et al. 2021. Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement. JAMA. 325(19):1965–77. 10.1001/jama.2021.6238. [DOI] [PubMed] [Google Scholar]
  • 4.Centers for Disease Control and Prevention. 2021. BRFSS Prevalence & Trends Data. https://www.cdc.gov/brfss/brfssprevalence/index.html. Accessed May 30, 2023.
  • 5.Star J, Bandi P, Siegel RL, Han X, Minihan A, Smith RA, et al. 2023. Cancer screening in the United States during the second year of the COVID-19 pandemic. Journal of Clinical Oncology. Epub Ahead of Print. 10.1200/JCO.22.02170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Fisher-Borne M, Isher-Witt J, Comstock S, Perkins RB. 2021. Understanding COVID-19 impact on cervical, breast, and colorectal cancer screening among federally qualified healthcare centers participating in "Back on track with screening" quality improvement projects. Preventive Medicine. 151:106681. 10.1016/j.ypmed.2021.106681. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Huguet N, Hodes T, Holderness H, Bailey SR, DeVoe JE, Marino M. 2022. Community Health Centers' performance in cancer screening and prevention. American Journal of Preventive Medicine. 62(2):e97–e106. 10.1016/j.amepre.2021.07.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Luque JS, Matthew OO, Jackson DR, Vargas MA, Austin T, Ali A, et al. 2022. Assessing the effectiveness of a community health advisor plus screen to save educational intervention on stool-based testing adherence in an African American safety net clinic population: study protocol for a randomized pragmatic trial. Trials. 23(1):151. 10.1186/s13063-022-06076-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Luque JS, Vargas M, Wallace K, Matthew OO, Tawk R, Ali AA, et al. 2022. Engaging the community on colorectal cancer screening education: focus group discussions among African Americans. Journal of Cancer Education. 37(2):251–62. 10.1007/s13187-021-02019-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.National Cancer Institute. 2018. National Cancer Institute, Health Information National Trends Survey. http://hints.cancer.gov/instrument.aspx. Accessed May 1, 2023.
  • 11.Morris NS, MacLean CD, Chew LD, Littenberg B. 2006. The Single Item Literacy Screener: evaluation of a brief instrument to identify limited reading ability. BMC Family Practice. 7:21. 10.1186/1471-2296-7-21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Balkrishnan R, Dugan E, Camacho FT, Hall MA. 2003. Trust and satisfaction with physicians, insurers, and the medical profession. Medical Care. 41(9):1058–64. 10.1097/01.MLR.0000083743.15238.9F. [DOI] [PubMed] [Google Scholar]
  • 13.Vernon SW, Myers RE, Tilley BC. 1997. Development and validation of an instrument to measure factors related to colorectal cancer screening adherence. Cancer Epidemiology, Biomarkers & Prevention. 6(10):825–32. [PubMed] [Google Scholar]
  • 14.Vernon SW, Meissner H, Klabunde C, Rimer BK, Ahnen DJ, Bastani R, et al. 2004. Measures for ascertaining use of colorectal cancer screening in behavioral, health services, and epidemiologic research. Cancer Epidemiology, Biomarkers & Prevention. 13(6):898–905. [PubMed] [Google Scholar]
  • 15.Kroenke K, Spitzer RL, Williams JB. 2003. The Patient Health Questionnaire-2: validity of a two-item depression screener. Medical Care. 41(11):1284–92. 10.1097/01.MLR.0000093487.78664.3C. [DOI] [PubMed] [Google Scholar]
  • 16.Kroenke K, Spitzer RL, Williams JB, Monahan PO, Lowe B. 2007. Anxiety disorders in primary care: prevalence, impairment, comorbidity, and detection. Annals of Internal Medicine. 146(5):317–25. 10.7326/0003-4819-146-5-200703060-00004. [DOI] [PubMed] [Google Scholar]
  • 17.Thompson VL, Bugbee A, Meriac JP, Harris JK. 2013. The utility of cancer-related cultural constructs to understand colorectal cancer screening among African Americans. Journal of Public Health Research. 2(2):e11. 10.4081/jphr.2013.e11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Vargas MA, Matthew OO, Jackson DR, Austin T, Tawk R, Wallace K, et al. 2021. Adaptation of a community health advisor intervention to increase colorectal cancer screening among African Americans in the southern United States. Cancer Health Disparities. 5 [Online]. https://companyofscientists.com/index.php/chd/article/view/204. [PMC free article] [PubMed] [Google Scholar]
  • 19.Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. 2009. Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support. Journal of Biomedical Informatics. 42(2):377–81. 10.1016/j.jbi.2008.08.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Muller C, Ihionkhan E, Stoffel EM, Kupfer SS. 2021. Disparities in early-onset colorectal cancer. Cells. 10(5). 10.3390/cells10051018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Brittain K, Christy SM, Rawl SM. 2016. African American patients' intent to screen for colorectal cancer: Do cultural factors, health literacy, knowledge, age and gender matter? Journal of Health Care for the Poor and Underserved. 27(1):51–67. doi: 10.1353/hpu.2016.00 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Hanske J, Meyer CP, Sammon JD, Choueiri TK, Menon M, Lipsitz SR, et al. 2016. The influence of marital status on the use of breast, cervical, and colorectal cancer screening. Preventive Medicine. 89:140–5. doi: 10.1016/j.ypmed.2016.05.017 [DOI] [PubMed] [Google Scholar]
  • 23.Adams LB, Richmond J, Corbie-Smith G, Powell W. 2017. Medical mistrust and colorectal cancer screening among African Americans. Journal of Community Health. 42(5):1044–61. 10.1007/s10900-017-0339-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Earl V, Beasley D, Ye C, Halpin SN, Gauthreaux N, Escoffery C, et al. 2022. Barriers and facilitators to colorectal cancer screening in African-American men. Digestive Diseases and Sciences. 67(2):463–72. 10.1007/s10620-021-06960-0. [DOI] [PubMed] [Google Scholar]
  • 25.Rawl SM, Christy SM, Perkins SM, Tong Y, Krier C, Wang HL, et al. 2021. Computer-tailored intervention increases colorectal cancer screening among low-income African Americans in primary care: Results of a randomized trial. Preventive Medicine. 145:106449. doi: 10.1016/j.ypmed.2021.106449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Roy S, Davis SN, Luque JS, Gwede CK. 2023. Colorectal Cancer. In Black Health in the South, eds. Coughlin SS, Williams LB, Akintobi TH. Baltimore, MD: Johns Hopkins University Press. [Google Scholar]

RESOURCES