Skip to main content
  • Research article
  • Open access
  • Published:

Collection of social determinants of health in the community clinic setting: a cross-sectional study



Addressing social and behavioral determinants of health (SBDs) may help improve health outcomes of community clinic patients. This cross-sectional study explored how assessing SBDs can be used to complement health data collection strategies and provide clinicians with a more in-depth understanding of their patients.


Adult patients, ages 18 and older, at an urban community health care clinic in Tennessee, U.S.A., were asked to complete a questionnaire regarding health status, health history and SBDs while waiting for their clinic appointment. The SBD component included items from the National Academy of Medicine, the Protocol for Responding to and Assessing Patient Assets, Risks, and Experiences instrument, and the Survey of Household Economics and Decisionmaking. Data collection and analysis occurred in 2017.


One hundred participants completed the study. The questionnaire took approximately 11 min to complete, and the response rate was 90% or higher for all items except annual household income (unanswered by 40 participants). The median number of negative SBDs was 4 (IQR 2.75–7.0), 96 participants had at least one unmet need, and the most common negative SBD was physical activity (75%; 75/100).


The hybrid questionnaire provided insight into a community clinic population’s SBDs and allowed for a more complete understanding than a single questionnaire alone. The brief questionnaire administration time and low non-response rate support the questionnaire’s feasibility in the community clinic setting, and results can be used by clinicians to further the personalization goals of precision medicine. Next steps include evaluating how to connect patients with appropriate resources for addressing their SBDs.

Peer Review reports


Community health centers provide care for low-income, medically underserved populations; these individuals are at greater risk of preventable, chronic disease and often report higher rates of chronic conditions, such as hypertension and diabetes [1, 2]. Understanding the role of social and behavioral determinants on health is particularly important for the care of community clinic patients and involves evaluating the impact of upstream factors affecting health, such as education, financial strain, and physical activity. Identifying and addressing social and behavioral determinants in the community clinic setting may represent one strategy for improving health outcomes of this population.

Standardized questionnaires have been developed to better understand patients’ social and behavioral needs. The National Academy of Medicine (NAM) formed a committee in 2013 which recommended a set of measures drawn from validated instruments for systematically collecting information about social and behavioral determinants of health (SBD) for incorporation into electronic health records in the United States [3,4,5]. The NAM instrument includes the following domains: race and ethnicity, education, financial resource strain, stress, depression, physical activity, tobacco use, alcohol use, social connection or isolation, intimate partner violence, residential address, and census-tract median income. The questionnaire’s performance was tested in two studies, in which the instrument was administered online to participants from across the United States [6, 7]. The studies supported the feasibility, reliability and validity of administering the NAM questionnaire based on the brief completion time (5 min), low non-response rate, lack of question order effects, establishment of test re-test reliability, and observations that response patterns were consistent with the literature and the measures were associated with self-reported physical and mental health [6, 7].

The Protocol for Responding to and Assessing Patient Assets, Risks, and Experiences (PRAPARE) is an instrument developed by the National Association of Community Health Centers and partners for use among United States community health care clinic populations that was designed to align with national social determinants of health initiatives [8, 9]. The PRAPARE instrument covers all domains included in the NAM questionnaire except depression, physical activity, and tobacco and alcohol use. It also includes additional domains not covered in the NAM questionnaire, including farmworker, veteran, housing, insurance, and refugee status, language preference, employment, transportation, neighborhood characteristics, material security (e.g., food, utilities, and clothing) [8] and incarceration history. When possible, questions included in PRAPARE were obtained from validated instruments [9]. Pilot studies were conducted in community health center networks in Hawaii, Iowa, New York, and Oregon, and cognitive testing was used to verify understanding of questions and ease of use [10,11,12]. Although the PRAPARE questionnaire has not yet been widely implemented in community clinics across the United States, questionnaire developers are currently engaged in implementation plans to facilitate its increased use [12, 13].

While previous studies have begun to assess social determinants of health in the community clinic setting [14, 15], we have not identified any published studies evaluating questionnaire performance in this population using standardized questionnaires, such as the NAM or PRAPARE questionnaires. Systematically capturing information about SBDs will be important to achieve the personalized care goals of precision medicine and help patients develop ways of overcoming upstream factors influencing their health.

In this study, we partnered with a local community health clinic to better understand the performance of a questionnaire for assessing patients’ social and behavioral needs. A hybrid questionnaire approach was chosen in order to gain a more complete understanding of patients’ social and behavioral needs than could be obtained from any single instrument. The questionnaire included all items from the PRAPARE, and items from the NAM SBD questionnaire that are not assessed in PRAPARE (depression, physical activity, and tobacco and alcohol use). Additionally, two items from the Federal Reserve Board’s Survey of Household Economics and Decisionmaking (SHED) were added to gain a better understanding of financial strain [16]. The SHED survey has been administered annually by the Federal Reserve Board since 2013 to a nationally representative adult population across the United States to ascertain the financial and economic status of the country. The primary objective of the study was to evaluate the feasibility of collecting social determinants of health data in the community clinic setting using the hybrid questionnaire approach and assess the prevalence of negative social and behavioral determinants of health.


Study setting and participants

This cross-sectional study was approved by the Vanderbilt University IRB (#162102) and took place at Connectus Health Vine Hill, a healthcare center serving the underinsured population in Nashville, Tennessee, U.S.A.. Recruitment was conducted from February 20 to March 3, 2017. Study team members recruited patients in the clinic waiting room. Patients aged 18 or older who were able to read and speak English were eligible to enroll and full, written informed consent was obtained prior to beginning study procedures. Patients received a $20 Walmart gift card for their participation. Data was collected via paper survey and entered into REDCap [17].

Study questionnaire

The study questionnaire was administered in the clinic waiting room. The health history and self-rated health status questions were adapted from the Centers for Disease Control and Prevention’s 2017 Behavioral Risk Factor Surveillance System Survey [18]. Participants were also asked to provide their age and gender identity.

The SBD component included all items from PRAPARE, including the optional questions regarding safety, domestic violence, incarceration history, and refugee status. Minor changes were made to a few of the questions for uniformity, clarity, and to aid understanding for individuals with limited health literacy. The changes included spelling out abbreviations, adding the text “please write” prior to the response line for the item regarding number of household members, and removing the text, “This information will help us determine if you are eligible for any benefits” from the item regarding income since it was not applicable for the study. For the social support question, which asks respondents to indicate the frequency of their interactions with people they care about, the response option “5 or more times a week” was replaced with “6 or more times a week” so that response options would not overlap. Yes/no checkboxes for the “other” option regarding material needs were removed since they were not applicable. The text “please write” was replaced with “please describe” prior to the open response options regarding employment and material needs to provide further clarity.

We also included items recommended by NAM that were not addressed in the PRAPARE tool, specifically, depression, physical activity, and tobacco and alcohol use [3]. The questions were added to ensure that information from all actionable domains was captured. To gain insight into participants’ financial strain, we included two questions from the SHED regarding how participants would pay for a hypothetical $400 emergency expense and the largest emergency expense they would be able to pay with money from their checking/savings account [16].

Statistical analysis

This pilot feasibility study used a convenience sample of one hundred participants with the goal of obtaining a cross-sectional representation of patients seen in the clinic during standard operating hours. All questionnaire responses were examined as outcome variables for the statistical analysis and missing data were excluded. Descriptive statistics were generated from study data using proportions and appropriate measures of central tendency (e.g., means with standard deviations, medians with interquartile ranges).

The depression, physical activity, tobacco use, and alcohol use items from the NAM questionnaire were scored as previously described by the study team [6]. Questionnaire responses about the number of family members and annual household income were used to calculate patient federal poverty levels (FPL) [19]. The following outcomes were included in the classification of negative SBDs: not having housing, housing instability, less than high school education, unemployed and not seeking work, uninsured, at or below 100% FPL, one or more unmet material needs, lack of transportation, social interaction fewer than three times a week, “quite a bit” or “very much” stress, positive depression screening, “inactive” or “insufficiently active” physical activity levels, current smoking status, positive alcohol use screening, inability to pay a $400 emergency with cash or its equivalent, history of incarceration, refugee status, physical or emotional unsafety, and history of domestic violence.

Associations between social determinant domains and age, gender, race, and health history were analyzed using Pearson chi-squared, Wilcoxon rank-sum, and Kruskal-Wallis tests. Spearman rank correlation coefficient and its p-value were also conducted to evaluate relationships between questionnaire domains. A two-tailed p-value less than 0.05 was considered significant and correlation strength was considered moderate or higher at ≥ 0.4 or ≤ − 0.4. All analyses were conducted in 2017 using R, version 3.3.2 or STATA/IC, version 12.1.


We approached 220 patients; 101 enrolled in the study and 119 declined to participate. Of those that declined, 31% (37/119) did not provide a specific reason other than not being interested, 29% (35/119) did not meet study language or age criteria, 23% (27/119) did not have time to complete the questionnaire, 8% (9/119) declined for privacy concerns, 7% (8/119) were not feeling well, and 3% (3/119) were anxious or upset about their clinic visit. The declining population was 22% male (26/119) and 78% female (93/119). One person started the questionnaire, paused for her clinic visit, then withdrew after her visit was over, citing lack of time to complete.

One hundred participants fully completed all study procedures. The study population was 67% female (67/100), 30% male (30/100), and 3% transgender (3/100). The median age of the participants was 38 years (IQR = 26.5–56.5). The two most prevalent self-reported health conditions were hypertension (45%; 45/100) and depression (39%; 39/100). Details on participants’ demographic characteristics, general health, and health histories are in Table 1.

Table 1 Participant characteristics and health history

The time to complete the questionnaire and non-response rate were assessed as indicators of feasibility. The final version of the survey contained 36 questions and the median time to complete was 11 min (IQR 8–16). Twenty-two percent (22/100) of participants began the questionnaire, paused for their clinic appointment, and finished it afterwards. With the exception of annual household income, which was left unanswered by 40 participants (40%), the response rate was 90% or higher on all items. Of the respondents that did not provide household income, 78% (31/40) could not afford to pay a $400 emergency with cash or its equivalent.

The most prevalent social determinant needs were in the domains of physical activity, financial strain, social integration and support, and stress (Table 2). Seventy-five percent (69/92) reported inactivity or insufficiently active exercise levels, 70% (70/100) were not able to use cash or cash-equivalent to pay for a $400 emergency expense, 45% (25/56) were at or below 100% FPL, 40% (40/100) had fewer than 3 social interactions/week, and 29% (29/100) experienced “quite a bit” or “very much” stress. The median number of negative SBDs (needs) was 4 (IQR 2.75–7.0) and overall, 96% (96/100) of participants had needs in one or more areas (Fig. 1). The total number of needs was significantly correlated with having one or more unmet material needs (r = 0.60; p < 0.001), an income at or below 100% federal poverty level (r = − 0.59; p < 0. 001), positive depression screening (r = .57; p < 0.001), appointments affected by lack of transportation (r = .46; p < 0. 001), and reporting “quite a bit/very much” stress (r = .46; p < 0. 001).

Table 2 Social determinants of health domains
Fig. 1
figure 1

Frequency distribution of social determinant needs

Several significant associations were identified between health conditions and SBDs. Hypertension was associated with having less than a high school education (p < 0.05), unemployment (p < 0.05), income at or below 100% FPL (p < 0.01), transportation issues (p < 0.05), and being unable to use cash or its equivalent to pay for a $400 emergency expense (p < 0.05). Those with a history of hypertension also had a higher median number of social needs than those without a history of hypertension (5 vs. 4; p < 0.05). A medical history of depression was associated with housing instability (p < 0.05), having one or more unmet material needs such as food, medicine, or clothing (p < 0.01), having quite a bit or very much stress (p < 0.001), and a positive screen for depression on the questionnaire (p < 0.01). Individuals with depression also had a higher median number of social needs than those without depression (6 vs. 3; p < 0.01).

Respondents’ general health was significantly correlated with age (r = − 0.46; p < 0.001) and tobacco use (r = − 0.41; p < 0.001). A few significant, moderate strength or higher correlations were also observed between responses to SBD items; higher stress was correlated with having a positive screening for depression (r = 0.51; p < 0.001), a positive screening for depression was correlated with having one or more unmet material security needs (r = 0.42; p < 0.001), and lower income levels were correlated to lower physical and emotional safety in the respondent’s current home environment (r = 0.41; p < 0.001).

Study team observation and direct patient interaction provided an opportunity to understand which questionnaire items participants may have had difficulty understanding or answering. For example, on the question asking about annual household income, 11/60 (18%) of participants responded with monthly rather than annual amounts. In response to the insurance question, three respondents wanted to provide more than one answer and five had difficulty classifying their insurance in one of the available categories (e.g., not knowing that their TennCare insurance is Tennessee’s Medicaid program). On the questionnaire item asking how many family members live in the household, five participants initially answered without counting themselves though the question instructions explicitly states to do so.


As rates of chronic illnesses rise across the nation [20], it is important to recognize the role of contributing social and behavioral factors and develop strategies to overcome them. Despite the availability of standardized measures for assessing social determinants of health, SBDs are still not routinely collected in medical practice. Responding to SBDs may help lessen the burden of chronic disease, resulting in improvements in quality of life, increased productivity, and lower health care costs [20, 21]. In states such as Tennessee, where our study was conducted, which have a high prevalence of chronic diseases, including hypertension, diabetes, and cardiovascular disease, addressing SBDs may have a profound impact on overall patient health and on healthcare services utilization [20, 22]. Rates of social and behavioral factors, including smoking, poverty, and lower educational attainment, are higher in Tennessee compared to the nation, and addressing SBDs may help improve the health of the state [20]. While extremely important in all medical settings, meeting patients’ social and behavioral health determinant needs becomes especially critical in community health care clinics. Screening for SBDs must occur at regular intervals, as needs will likely change over time. A necessary next step will be to assess how to help connect individuals with appropriate agencies and resources.

Our study supports the feasibility of administering a social determinants of health questionnaire in the community clinic setting. Most participants were able to complete the questionnaire while waiting for their clinic appointment. The time needed to complete the questionnaire was slightly longer than PRAPARE’s approximate nine minutes, reflecting the inclusion of additional questions. The non-response rate was low for most questionnaire items, with the exception of annual household income.

Responses to the general health questionnaire were consistent with previously-reported data from community clinic populations [23]. The most prevalent negative SBDs were physical activity, financial strain, social integration and support, and stress. Widespread use of standardized SBD questionnaires will enable a better understanding of differences in negative SBDs among different populations. The finding regarding a high prevalence of financial strain was expected, given that the clinic cares for a medically underserved population, where many individuals fall below the federal poverty level [2]. The low rate of alcohol use may reflect the high prevalence of women visiting the clinic for pregnancy-related care in our sample. Associations between health conditions and negative SBDs and associations between SBD domains were also consistent with the literature, further supporting use of the hybrid questionnaire [6, 7, 24].

Results from this pilot study suggest that some questions may need modifications before wide implementation. The question regarding annual household income was unanswered by 40% of participants. Of participants who responded to the question, 20% provided monthly rather than annual amounts. Based on the high non-response rate and the difficulty with answering the question, an alternative approach to understanding financial strain may be needed. Census-tract median income has been used as a way to obtain neighborhood-level information and overcome the sensitivity of asking about household income [3]. However, one of the limitations of this approach is that it may not adequately represent the characteristics of the individual. Additionally, racial minorities and individuals with low incomes are often underrepresented in the U.S. Census, which further compromises reliance on this data for understanding characteristics of these populations [25,26,27]. As recently as November 2017, the Huffington Post reported on the potential negative impact of inaccurate census data on vulnerable communities [28]. The U.S. Census underrepresentation is strikingly apparent when looking at a geographic visualization of “hard-to-count” communities in Nashville, as census-tract areas with higher populations of racial minorities and low-income households display the lowest 2010 census return rates [29]. Another option for assessing financial strain at the individual level is the use of the selected questions from the SHED (Survey of Household Economics and Decisionmaking), for which we observed a high response rate.

The questions regarding insurance and household composition used in our questionnaire may also need refinement. A few participants wanted to select more than one answer to the question regarding insurance, and several had difficulty determining to which category their insurance applied. For the question regarding the number of family members living in the household, a few participants did not include themselves in the count, although the question explicitly indicates to do so, suggesting that the instructions may need to be made clearer.

Limitations of our study include the use of self-reported data and reliance on a convenience sample recruited from a single, urban community health clinic. The majority of participants who enrolled in the study were female. Future studies should aim for a nationally representative demographic sample. While our specific findings regarding the prevalence and type of negative SBDs may not be generalizable to clinics across the United States, our study confirms the feasibility of administering the questionnaire in the community clinic setting. Additional studies are needed to evaluate the impact of questionnaire administration on clinic workflow and incorporation into the electronic health record. LOINC codes have been developed to represent SBD variables; however, a recent 3-year retrospective review of medical records of more than 1 million patients in the nation’s largest health information exchange network found that the social determinant LOINC codes were not being used [30, 31].


This study supports the feasibility of assessing social and behavioral determinants of health in the community clinic setting. By screening for social determinants of health, providers can obtain a better glimpse of patients’ underlying needs and factors affecting their health. Routine screening for social determinants of health will aid in the implementation of precision medicine, which goes beyond an understanding of a person’s genetic composition to incorporate each patient’s environment and lifestyle to develop individualized treatments. The hybrid questionnaire used in our study provides a more complete view of the patient than through any single instrument. The implementation of the questionnaire will provide insight into a wide range of patient social and behavioral health determinant needs, which will quickly inform providers about the most salient personal and socioeconomic issues of each patient and which domains may require additional probing. Our study has helped reveal top need areas among the community clinic patients that were surveyed, and future studies are planned to evaluate how to connect patients with community and public health resources to help address identified needs.



federal poverty level


interquartile range


Logical Observation Identifiers Names and Codes


National Academy of Medicine


Protocol for Responding to and Assessing Patient Assets, Risks, and Experiences


social and behavioral determinants of health


Survey of Household Economics and Decisionmaking


  1. HRSA Health Center Program. What is a health center? Health Resources & Services Administration. Accessed 8 Mar 2018.

  2. Kaiser Commission on Medicaid and the Uninsured. Community health centers: the challenge of growing to meet the need for primary care in medically underserved communities. 2012. Accessed 8 Mar 2018

  3. Committee on the Recommended Social and Behavioral Domains and Measures for Electronic Health Records, Board on Population Health and Public Health Practice, Institute of Medicine. Capturing social and behavioral domains and measures in electronic health records: phase 2. 2014. Accessed 8 Mar 2018.

  4. Adler NE, Stead WW. Patients in context--EHR capture of social and behavioral determinants of health. N Engl J Med. 2015;372:698–701.

    Article  CAS  PubMed  Google Scholar 

  5. Matthews KA, Adler NE, Forrest CB, Stead WW. Collecting psychosocial “vital signs” in electronic health records: why now? What are they? What’s new for psychology? Am Psychol. 2016;71:497–504.

    Article  PubMed  Google Scholar 

  6. Giuse NB, Koonce TY, Kusnoor SV, Prather AA, Gottlieb LM, Huang L, et al. Institute of Medicine measures of social and behavioral determinants of health: a feasibility study. Am J Prev Med. 2017;52:199–206.

    Article  PubMed  Google Scholar 

  7. Prather AA, Gottlieb LM, Giuse NB, Koonce TY, Kusnoor SV, Stead WW, et al. National Academy of medicine social and behavioral measures: associations with self-reported health. Am J Prev Med. 2017;

  8. National Association of Community Health Centers. PRAPARE (version date September 20, 2016). National Association of Community Health Centers website. 2017. Accessed 8 Mar 2018.

  9. Slides for Collecting Social Determinants of Health Data with PRAPARE Presentation 4–20-16. Healthcare Communities website. 2016. Available from: Accessed 8 Mar 2018.

  10. PRAPARE Frequently Asked Questions. National Association of Community Health. Centers website. 2016. Available from: Accessed 8 Mar 2018.

  11. PRAPARE abstract & LC overview 2.26.15. Healthcare Communities website. 2015. Available from: d=88097. Accessed 8 Mar 2018.

  12. LaForge K, Gold R, Cottrell E, Bunce AE, Proser M, Hollombe C, et al. How 6 organizations developed tools and processes for social determinants of health screening in primary care: an overview. J Ambul Care Manage. 2018;41:2–14.

    Article  PubMed  Google Scholar 

  13. National Association of Community Health Centers. PRAPARE Implementation and Action Toolkit. National Association of Community Health Centers website. Accessed 6 Mar 2018.

  14. Garg A, Toy S, Tripodis Y, Silverstein M, Freeman E. Addressing social determinants of health at well child care visits: a cluster RCT. Pediatrics. 2015;135:e296–304.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Waitzkin H, Getrich C, Heying S, Rodríguez L, Parmar A, Willging C, et al. Promotoras as mental health practitioners in primary care: a multi-method study of an intervention to address contextual sources of depression. J Community Health. 2011;36:316–31.

    Article  PubMed  Google Scholar 

  16. Board of Governors of the Federal Reserve Board. Report on the economic well-being of U.S. households in 2016. Board of Governors of the Federal Reserve System. 2017. Accessed 6 Mar 2018.

  17. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42:377–81.

    Article  PubMed  Google Scholar 

  18. Centers for Disease Control and Prevention. BRFSS questionnaires. Behavioral Risk Factor Surveillance System website. 2017. Accessed 6 Mar 2018.

  19. Office of the Federal Register. Federal Register - annual update of the HHS poverty guidelines. Federal Register 2017. Accessed 6 Mar 2018

  20. Sycamore Institute. The economic impact of chronic disease in Tennessee. The Sycamore Institute. 2017. Accessed 6 Mar 2018.

  21. Cockerham WC, Hamby BW, Oates GR. The social determinants of chronic disease. Am J Prev Med. 2017;52(1S1):S5–12.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Centers for Disease Control & Prevention. Division of diabetes translation. Long-term trends in diabetes. 2017. Accessed 6 Mar 2018.

  23. Shin P, Alvarez C, Sharac J, Rosenbaum S, Van Vleet A, Paradise J, et al. A profile of community health center patients: implications for policy. The Henry J. Kaiser Family Foundation. 2013. Accessed 8 Mar 2018.

  24. Braveman P, Gottlieb L. The social determinants of health: it’s time to consider the causes of the causes. Public Health Rep. 2014;129(Suppl 2):19–31.

    Article  PubMed  PubMed Central  Google Scholar 

  25. US Census Bureau Public Information Office. Census Bureau releases estimates of undercount and overcount in the 2010 Census. United States Census Bureau. 2012. Accessed 8 Mar 2018.

  26. Dade C. Census Bureau rethinks the best way to measure race. Nashville Public Radio. 2012; Accessed 8 Mar 2018

  27. Schless-Meier A, Bass GD. An insidious way to underrepresent minorities. Am Prospect. 2015; Accessed 8 Mar 2018

  28. Levine S. Experts are really, really worried about the state of the 2020 census. Huffington Post. 2017; Accessed 8 Mar 2018

  29. City University of New York Center for Urban Research. Census 2020 Hard to Count Map. Hard to Count 2020 website. Accessed 8 Mar 2018.

  30. Regenstrief Institute. LOINC: social determinants of health. Accessed 8 Mar 2018.

  31. Cullen T, Allen K, Armson S, Roberts A, Vreeman DJ. The capture of social and behavioral determinants of health in electronic health records. American Medical Informatics Association 2017 Annual symposium. Washington, DC; 2017. Accessed 8 Mar 2018.

Download references


The authors wish to thank Annette Williams, MLS and Zachary Fox, MSIS for their editorial assistance with the manuscript. Partial findings from this study were presented as a poster at the 2017 Annual Symposium of the American Medical Informatics Association.


Support for the REDCap database, used in this study for data entry and data collection, was provided by CTSA award UL1TR000445 from the National Center for Advancing Translational Sciences. Funding for participant compensation was also provided by CTSA Award UL1TR000445 as part of the voucher program of the Vanderbilt Institute for Clinical and Translational Research (#VR23877).

Availability of data and materials

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Author information

Authors and Affiliations



This study was conceptualized by the entire authorship team and led by NG. SH provided specific insight into the clinic patient population and contributed feedback on the patient interview process. TK, KM, ME, MB, and EF recruited participants at the Vine Hill Clinic. Descriptive and statistical analyses were conducted by LH, SK, and TK. The manuscript was written collaboratively by SK, TK, and NG, and all authors critically reviewed and edited the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sheila V. Kusnoor.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the Vanderbilt University IRB (#162102). Written informed consent was required for participation in the study.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kusnoor, S.V., Koonce, T.Y., Hurley, S.T. et al. Collection of social determinants of health in the community clinic setting: a cross-sectional study. BMC Public Health 18, 550 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: