Published on in Vol 10 (2024)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/52762, first published .
Factors Associated With Surveillance Testing in Individuals With COVID-19 Symptoms During the Last Leg of the Pandemic: Multivariable Regression Analysis

Factors Associated With Surveillance Testing in Individuals With COVID-19 Symptoms During the Last Leg of the Pandemic: Multivariable Regression Analysis

Factors Associated With Surveillance Testing in Individuals With COVID-19 Symptoms During the Last Leg of the Pandemic: Multivariable Regression Analysis

1West Virginia Clinical and Translational Sciences Institute, , Morgantown, WV, , United States

2Department of Management Information Systems, West Virginia University, , Morgantown, WV, , United States

3Department of Public Health Sciences, College of Behavioral, Social, and Health Sciences, Clemson University, , Clemson, SC, , United States

4American Diabetes Association, , Arlington, VA, , United States

5School of Medicine, West Virginia University, , Morgantown, WV, , United States

6Center for Rural and Community Health, West Virginia School of Osteopathic Medicine, , Lewisburg, WV, , United States

Corresponding Author:

Timothy Dotson, MS


Background: Rural underserved areas facing health disparities have unequal access to health resources. By the third and fourth waves of SARS-CoV-2 infections in the United States, COVID-19 testing had reduced, with more reliance on home testing, and those seeking testing were mostly symptomatic.

Objective: This study identifies factors associated with COVID-19 testing among individuals who were symptomatic versus asymptomatic seen at a Rapid Acceleration of Diagnostics for Underserved Populations phase 2 (RADx-UP2) testing site in West Virginia.

Methods: Demographic, clinical, and behavioral factors were collected via survey from tested individuals. Logistic regression was used to identify factors associated with the presence of individuals who were symptomatic seen at testing sites. Global tests for spatial autocorrelation were conducted to examine clustering in the proportion of symptomatic to total individuals tested by zip code. Bivariate maps were created to display geographic distributions between higher proportions of tested individuals who were symptomatic and social determinants of health.

Results: Among predictors, the presence of a physical (adjusted odds ratio [aOR] 1.85, 95% CI 1.3-2.65) or mental (aOR 1.53, 95% CI 0.96-2.48) comorbid condition, challenges related to a place to stay/live (aOR 307.13, 95% CI 1.46-10,6372), no community socioeconomic distress (aOR 0.99, 95% CI 0.98-1.00), no challenges in getting needed medicine (aOR 0.01, 95% CI 0.00-0.82) or transportation (aOR 0.23, 95% CI 0.05-0.64), an interaction between community socioeconomic distress and not getting needed medicine (aOR 1.06, 95% CI 1.00-1.13), and having no community socioeconomic distress while not facing challenges related to a place to stay/live (aOR 0.93, 95% CI 0.87-0.99) were statistically associated with an individual being symptomatic at the first test visit.

Conclusions: This study addresses critical limitations to the current COVID-19 testing literature, which almost exclusively uses population-level disease screening data to inform public health responses.

JMIR Public Health Surveill 2024;10:e52762

doi:10.2196/52762

Keywords



Pandemic Spread

The SARS-CoV-2 pandemic has had several waves of infection driven by the introduction and spread of multiple variants. In the United States, the first case of COVID-19 appeared in January 2020 [1]. The Alpha variant, first introduced in December 2020, comprised the second wave of the COVID-19 pandemic, occurring at the same time as vaccination campaigns were being rolled out in many states [2]. This was a critical moment in the SARS-CoV-2 timeline, as Alpha was the first variant of concern with adapted mutations, increasing the risk of person-to-person transmission [3]. The pattern of spread and speed of the third and fourth waves involving Omicron variants (BA1-3 and BA4-5) were wider reaching and faster than previous variants [4]. Unfortunately, this was problematic with reduced testing efforts making it more difficult to monitor SARS-CoV-2 infections in populations [5].

Health Disparities

Urban US areas experienced the greatest burden of cases early in the epidemic with West Virginia, a largely rural state, being the last state to identify a confirmed case of COVID-19 in late January 2020. This is problematic as 50% of rural residents are at high risk of serious illness and hospitalization if they contract SARS-CoV-2 [6]. In West Virginia, the Alpha variant cases peaked in April 2021, 4 months after its initial detection in the United States and after vaccination campaigns were already underway, with subsequent peaks in October 2021 for the Delta variant and February 2022 for the first Omicron peak. Due to unequal access to health resources, the impacts of the disease vary throughout the state, particularly in southwest West Virginia where there are already health disparities [7].

Prior Work

By August 2020, testing in the United States had peaked at around 1 million tests per day, at which point COVID-19 had become the third leading cause of death [1]. COVID-19 testing data have been used in machine learning models and spatial epidemiological studies to help identify disparities in testing and outcomes for COVID-19, and guide public health policies [8-10]. Previous studies have analyzed socioeconomic status, race, comorbidities, mental health, and substance abuse effects to identify disparities and seasonal impacts [7,9-14]. Furthermore, other epidemic models have been tested using COVID-19 data to help forecast future SARS-CoV-2 waves and look at the impact of testing itself [11,12]. However, previous research was conducted during times with high-to-moderate community testing, when data more accurately reflected the general population’s risk of disease and allowed for standard epidemiological models of study [1,13-15]. The pandemic is now in a phase where those seeking testing are largely symptomatic. Lower testing and increasing reliance on home testing for COVID-19 have created a situation in which traditional epidemiological measures are suboptimal [16].

Study Objectives

Subsequent waves of SARS-CoV-2 infection are now monitored with varying surveillance efforts, which have dwindled from the population to the community level as the focus shifted away from testing to preventing severe infection and health care strain [5]. This situation has resulted in a heightened reliance on testing data from people who are symptomatic and seek out testing. Currently, few studies have examined the demographics, clinical factors, or barriers to testing among people who are symptomatic and seeking COVID-19 testing [15,17]. As such, the objectives of this study were to identify factors that increased the prevalence of individuals who were symptomatic at testing locations and assess whether there was spatial autocorrelation among the rate of tested people who were symptomatic and their residential zip code. Spatial autocorrelation, or clustering of tested people who were symptomatic, was assessed to better understand if geographic differences in hospital or doctor referrals potentially biased the number of people who were symptomatic who visited testing locations [18,19]. The results address current literature gaps concerning which factors are associated with test seeking and have the potential to inform public health policy to ensure COVID-19 testing services remain available to vulnerable populations living in the rural United States.


Data Source and Management

This cross-sectional study utilized questionnaire data collected for phase 2 of the Rapid Acceleration of Diagnostics for Underserved Populations program (RADx-UP2). Detailed information on RADx-UP2, including program aims and research projects, has been described elsewhere [20]. Briefly, RADx-UP is a multisite National Institutes of Health–funded project, developed to disseminate testing resources within communities of varying social or economic vulnerability [21]. All sites are required to include common data elements (CDEs) in their data collection instruments to harmonize data across states [21]. Project CDEs include an individual’s address, demographics, clinical comorbidities, signs and symptoms at the time of testing, behavioral data, and more [21]. For the West Virginia site, data were collected using ArcGIS Survey 123 (Esri) at testing events. The benefits of using syndromic surveillance for public health programming and response have been described in previous public health research elsewhere [16,22-24].

Ethical Considerations

Approval for this study was given by the West Virginia University Institutional Review Board (protocol 2202534378A001). Informed consent was requested on the survey used for data collection in the form of an opt-out question. All included data has been deidentified for analysis and publication. Site-level incentives were developed in conjunction with community partners that assisted in hosting testing events. As such, these incentives varied by site and community and consisted of monthly raffles for all who participated in a survey during that month for each testing site, with prizes including technology, tickets to sporting events, and outdoor items. Other incentives included t-shirts and plastic reusable cups for participation.

Inclusion Criteria

The study inclusion criteria were any individual tested at a West Virginia RADx-UP2 testing site from May 2022 until November 2022. Testing sites included pharmacies, hospitals, and homeless shelters in underserved areas throughout the state manned by RADx-UP2 staff as well as at testing events such as Solutions Oriented Addiction Response (SOAR) meetings and other community-sponsored events. Individuals seeking COVID-19 testing paid for by RADx-UP funding and consented to have their information collected. For this study, the analytic sample was limited to information collected at each individual’s first test, including the individual’s demographics, signs and symptoms, history of chronic disease, receipt of two vaccine doses, and challenges or motivators to seek care. The study outcome was the odds of an individual who was symptomatic (vs asymptomatic) being seen at the time of first testing. Individuals who were symptomatic presented with one of the following at the time of testing: fever or chills, cough, shortness of breath or difficulty breathing, lack of energy or general tired feeling, muscle or body aches, headache, new loss of taste or smell, sore throat/congestion or runny nose, feeling sick to your stomach or vomiting/diarrhea, abdominal pain, or skin rash.

Predictor Covariates

Predictor covariates in the analysis included age categories (<18, 19‐29, 30‐39, 40‐49, 50‐59, and ≥60 years), race, sex at birth, whether a person is an essential worker, whether a person is fully vaccinated (eg, received two doses of Moderna/Pfizer or one dose of Johnson & Johnson), presence/absence of physical or mental health conditions (yes/no), six challenges to health (yes/no), specific barriers to testing (yes/no), and a measure of economic distress based on the individual’s zip code of residence to adjust for nonrandom community-level effects. Physical health conditions, mental health conditions, and barriers to testing were combined into their groupings due to the small sample size of the individual and missingness in the subgroups. Physical health conditions included immunocompromised condition, autoimmune disease, hypertension, diabetes, chronic kidney disease, cancer diagnosis or treatment within the past 12 months, cardiovascular disease, asthma, chronic obstructive pulmonary disease, other chronic lung disease, and sickle cell anemia. Mental health conditions included depression, alcohol or substance use disorder, intravenous drug use, and other mental health disorders. The six challenges to health included access to mental/physical health care, having a place to stay/live, getting enough food to eat, having clean water to drink, getting the medicine needed, and having transportation from one place to another. Barriers to testing included protected time off to visit a testing site; out-of-pocket costs for test; out-of-pocket costs for transportation, childcare, or time off work to get tested; knowledge of where testing is done in their community; pain or discomfort from the test or saliva collection; and concern about others handling their personal data. All predictor covariates, except for the economic distress score, were collected as CDEs required for all funded RADx-UP2 projects [21]. The zip code–level Distressed Communities Index (DCI) was linked to survey data by individual zip code of residence to adjust for nonrandom selection of underserved communities for testing. The DCI is a measurement of community economic disparities that consists of seven measures obtained from the US Census Bureau’s American Community Survey: no high school diploma, housing vacancy rate, adults not working, poverty rate, median income ratio, changes in employment, and changes in establishments. This was critical as RADx-UP2 nonrandomly selects communities for testing based on whether they are underserved. DCI was a continuous variable, where higher numbers indicated more distress [25]. This index of socioeconomic deprivation has been utilized in previous social epidemiology literature to characterize health disparities [26,27].

Statistical Analysis

Data were analyzed by multivariable logistic regression to evaluate the association between the odds of an individual being symptomatic at the time of the first test and each of the predictors. Interaction effects between the six challenges to health and the DCI were also included in the multivariable logistic regression model, and backward selection with Akaike information criterion was used to ensure the best covariates model was used adjusting for age, gender, and race after selection. Statistical significance was evaluated using adjusted odds ratios (aORs) and corresponding 95% CIs at an α level of .05. Tests for global spatial autocorrelation (clustering) of individuals who were symptomatic were conducted using a global Moran I value. Statistical spatial dependence was evaluated using the tests’ computed z score and P value [28]. All data management and regression analyses were conducted in R (The R Foundation for Statistical Computing). Spatial analysis and thematic maps displaying zip code–level relationships between the rate of people who were symptomatic per 10 individuals tested and the distressed communities score were created in ArcGIS Pro 2.9.2 (Esri).


Data Source and Management

Of the 2103 testing questionnaires completed between May 7 and November 14, 2022, 1423 unique individuals were identified as having self-reported as being symptomatic at the time of their first test (Table 1). In the overall sample, 24.5% (n=348) were 60 years or older, 85.5% (n=1217) were White, and 51.7% (n=735) were female. The majority of individuals were vaccinated (n=975, 68.5%), did not report any physical (n=773, 54.3%) or mental (n=1120, 78.7%) health conditions, and did not have any of the six challenges to health: access to health care (n=1155, 81.2%), place to stay/live (n=1162, 81.7%), enough food to eat (n=1198, 84.2%), clean water to drink (n=1228, 86.3%), getting needed medication (n=1163, 81.7%), and having transportation (n=1165, 81.9%). Among individuals who were symptomatic, 26.6% (n=219) were 60 years or older, 87.1% (n=717) were White, and 55.8% (n=459) were female. Similar to the overall sample, the majority of individuals who were symptomatic were vaccinated (n=581, 70.6%), did not report any physical (n=418, 50.8%) or mental (n=656, 79.7%) health issues, and did not have any of the six challenges to health: access to health care (n=736, 89.4%), place to stay/live (n=746, 90.6%), enough food to eat (n=759, 92.2%), clean water to drink (n=773, 93.9%), getting needed medication (n=741, 90%), and having transportation (n=747, 90.8%).

Table 1. Demographics and clinical characteristics of individuals tested for SARS-CoV-2 during phase 2 of the Rapid Acceleration of Diagnostics for Underserved Populations program. The program took place between May 7 and November 14, 2022, and tested 1423 unique individuals who self-reported as being symptomatic at the time of their first test.
VariableIndividuals, n (%)Clinical symptoms, n (%)
Nonsymptomatic (n=600)Symptomatic (n=823)
Age (years)
≤18285 (20.0)110 (18.3)175 (21.3)
19-29143 (10.0)51 (8.5)92 (11.2)
30-39208 (14.6)100 (16.7)108 (13.1)
40-49188 (13.2)92 (15.3)96 (11.7)
50-59164 (11.5)74 (12.3)90 (10.9)
≥60348 (24.5)129 (21.5)219 (26.6)
Missing87 (6.1)44 (7.3)43 (5.2)
Race
White1217 (85.5)500 (83.3)717 (87.1)
Black/African American114 (8.0)61 (10.2)53 (6.4)
Other67 (4.7)33 (5.5)34 (4.1)
Missing25 (1.8)6 (1.0)19 (2.3)
Sex at birth
Female735 (51.7)276 (46.0)459 (55.8)
Male651 (45.7)307 (51.2)344 (41.8)
Missing37 (2.6)17 (2.8)20 (2.4)
Essential worker
No990 (69.6)429 (71.5)561 (68.2)
Yes319 (22.4)118 (19.7)201 (24.4)
Missing114 (8.0)53 (8.8)61 (7.4)
Vaccinated
No392 (27.5)182 (30.3)210 (25.5)
Yes975 (68.5)394 (65.7)581 (70.6)
Missing56 (3.9)24 (4.0)32 (3.9)
Physical health condition
No773 (54.3)355 (59.2)418 (50.8)
Yes472 (33.2)168 (28.0)304 (36.9)
Missing178 (12.5)77 (12.8)101 (12.3)
Mental health condition
No1120 (78.7)464 (77.3)656 (79.7)
Yes233 (16.4)110 (18.3)123 (14.9)
Missing70 (4.9)26 (4.3)44 (5.3)
Challenges to health
Access to health care
No1155 (81.2)419 (69.8)736 (89.4)
Yes232 (16.3)173 (28.8)59 (7.2)
Missing36 (2.5)8 (1.3)28 (3.4)
Place to stay/live
No1162 (81.7)416 (69.3)746 (90.6)
Yes216 (15.2)171 (28.5)45 (5.5)
Missing45 (3.2)13 (2.2)32 (3.9)
Enough food to eat
No1198 (84.2)439 (73.2)759 (92.2)
Yes185 (13.0)150 (25.0)35 (4.3)
Missing40 (2.8)11 (1.8)29 (3.5)
Clean water to drink
No1228 (86.3)455 (75.8)773 (93.9)
Yes159 (11.2)136 (22.7)23 (2.8)
Missing36 (2.5)9 (1.5)27 (3.3)
Getting needed medicine
No1163 (81.7)422 (70.3)741 (90.0)
Yes212 (14.9)162 (27.0)50 (6.1)
Missing48 (3.4)16 (2.7)32 (3.9)
Transportation
No1165 (81.9)418 (69.7)747 (90.8)
Yes206 (14.5)165 (27.5)41 (5.0)
Missing52 (3.7)17 (2.8)35 (4.3)
Barriers to testing
No519 (36.5)195 (32.5)324 (39.4)
Yes460 (32.3)203 (33.8)257 (31.2)
Missing444 (31.2)202 (33.7)242 (29.4)

Statistical Analysis

In the parsimonious model, backward selection with Akaike information criterion dropped the following variables: essential worker, vaccinated, and access to health care. Among persons at the time of first testing, all age groups, races, sex at birth, barriers to testing, enough food to eat, clean water to drink, and the DCI and clean water to drink interaction were not statistically associated with the odds of seeing an individual who was symptomatic at a testing location (all P values >.05). Individuals with a physical health condition and challenges related to a place to stay/live were statistically more likely to seek testing while being symptomatic, and mental health condition and the DCI and getting needed medicine interaction were moderately so. Those reporting physical health conditions were 85% more likely to have reported being symptomatic (aOR 1.85, 95% CI 1.3-2.65), and those reporting challenges of having a place to stay/live were 307.13 times more likely to have reported being symptomatic (aOR 307.13, 95% CI 1.46-106,372). Those reporting mental health conditions were 53% more likely to have reported being symptomatic (aOR 1.53, 95% CI 0.96-2.48), and those living in a high DCI zip code while also not getting needed medicine were 6% more likely to have reported being symptomatic (aOR 1.06, 95% CI 1.00-1.13). Individuals with a challenge getting needed medicine and transportation as well as the DCI and challenges in having a place to stay/live interaction were statistically less likely to seek testing while symptomatic, and living in a high DCI zip code was moderately so. Participants who had challenges in getting needed medication were 99% less likely to report being symptomatic (aOR 0.01, 95% CI 0.00-0.82). Those who had challenges with transportation were 77% less likely to report being symptomatic (aOR 0.23, 95% CI 0.05-0.64). Those living in a high DCI zip code and facing challenges of having a place to stay/live were 7% less likely to report being symptomatic (aOR 0.93, 95% CI 0.87-0.99), and those living in a high DCI zip code were 1% less likely to seek testing as a symptomatic individual (aOR 0.99, 95% CI 0.98-1.00). Complete results for the logistic regression are displayed in Table 2.

Table 2. Adjusted odds ratios and corresponding 95% CIs for logistic regression models. Full discussion of results can be found in the Results: Statistical Analysis section. The parsimonious model was derived using backward selection from the original model. A full description of the procedure can be found in the Methods: Statistical Analysis section.
VariableOriginal modelParsimonious model
Adjusted odds ratio95% CIAdjusted odds ratio95% CI
Age (years)
≤181.60.9-2.91.640.94-2.92
19-29 (reference)1a1
30-390.830.51-1.370.850.52-1.4
40-490.970.57-1.670.980.58-1.68
50-590.750.42-1.330.730.42-1.3
≥600.720.44-1.170.690.43-1.1
Race
White (reference)11
Black/African American0.670.39-1.160.680.4-1.17
Other0.70.37-1.370.710.37-1.37
Sex at birth
Female (reference)11
Male0.870.64-1.170.870.65-1.17
Essential worker
No (reference)11
Yes1.10.76-1.59
Vaccinated
No (reference)11
Yes0.880.61-1.27
Physical health condition
No (reference)11
Yes1.871.31-2.681.851.3-2.65
Mental health condition
No (reference)11
Yes1.591-2.61.530.96-2.48
Challenges to health
Access to health care
No (reference)11
Yes0.520-1510
Place to stay/live
No (reference)11
Yes1420.08-1,151,363307.131.46-106,372
Enough food to eat
No (reference)11
Yes0.010-17932.710.79-10.27
Clean water to drink
No (reference)11
Yes410.06-71,082660.12-112,368
Getting needed medicine
No (reference)11
Yes0.010-56.80.010-0.82
Transportation
No (reference)11
Yes3210.01-22,493,6900.230.08-0.64
Barriers to testing
No (reference)11
Yes1.310.95-1.81.290.94-1.77
Distress score0.990.98-10.990.98-1

aNot applicable.

Geospatial Analysis

A bivariate map of the zip code–level rate of individuals who were symptomatic per 10 individuals seeking COVID-19 testing and the DCI is displayed in Figure 1. Visually, there appear to be overlapping trends in the DCI and rate of people who are symptomatic per 10 people served at testing locations in the southern and northern regions of West Virginia. In particular, southern West Virginia had more zip codes where the rate of tested people who were symptomatic was low and the DCI was low, indicating fewer people who were symptomatic from nondistressed communities when compared to the rest of the state. There was only 1 zip code in the northern region of West Virginia that followed this trend. However, both regions had zip codes where the rate of tested people who were symptomatic per 10 individuals was high and the DCI score was high, indicating a high number of people who were symptomatic coming from distressed communities. In the southern region, there were many zip codes with a high DCI score but a low rate of people who were symptomatic. This visual observation supports findings from the logistic regression that the DCI was statistically associated with a lower rate of tested people who were symptomatic, particularly for persons in southern West Virginia. When assessing spatial autocorrelation, global Moran I did not detect any statistically significant clustering in the rate of people who were symptomatic per 10 individuals tested throughout the RADx-UP study area. Statistically significant clustering was evaluated incrementally across distance thresholds of varying diameters (smallest: 357 km, Moran I=0.002, P=.63; largest: 784 km, Moran I=0.001, P=.06) without indication of statistical significance.

Figure 1. Rate of individuals who were symptomatic per 10 individuals seeking COVID-19 testing at a Rapid Acceleration of Diagnostics for Underserved Populations phase 2 program testing site between May 7 and November 14, 2022, in West Virginia by zip code.

Principal Results

This study identified several factors associated with test seeking among individuals who were symptomatic at RADx-UP2 COVID-19 testing locations. Our study found that individuals with a physical or mental health condition, those facing a challenge in having a place to stay/live, or those with the interaction of living in a high DCI zip code while also not getting needed medicine were more likely to appear at a testing location with symptoms. Additionally, individuals from less distressed communities, who were able to access needed medicine or transportation, and those with the interaction of living in a high DCI zip code and facing challenges in having a place to stay/live were less likely to be symptomatic at the time of their testing. Importantly, we found no statistically significant geographic pattern in the rate of people who were symptomatic per 10 individuals tested. This could suggest that differences observed for persons less likely to be symptomatic by a higher DCI were not due to geographic contexts, such as urban or rural, and perhaps more related to social determinants of health such as facing a challenge in having a place to stay/live within the individual’s zip code of residence. Importantly, these findings address a gap in the existing literature, particularly among studies that utilize recent testing data within epidemiological investigations by looking at underserved areas and the reasoning behind individuals seeking testing [15,17]. Recent testing data reflect a shift toward symptomatic populations who are more likely to struggle with a stable living situation and experience multiple physical or mental health conditions. This is an important consideration, as new information from this study provides an idea of the extent to which the generalizability of testing data is restricted to vulnerable populations or those separate from the general population.

Physical and Mental Health Conditions

Physical and mental health conditions were found to be associated with individuals presenting with symptoms for COVID-19 testing. Physical health conditions, such as autoimmune disease, hypertension, diabetes, chronic kidney disease, and cardiovascular disease, can cause impediments to the immune system and leave individuals more susceptible to severe illnesses, including COVID-19 [29,30]. These individuals may be more willing to seek out testing when they become symptomatic due to their increased risk of serious illness [4,15,27,29,30]. Altogether these individuals would be more likely to be symptomatic when reporting to testing facilities, whether due to the increased risk of the physical conditions themselves or as a preventative measure taken by the individuals. Additionally, mental health conditions, such as alcohol and substance use, can also increase an individual’s susceptibility to infection from and exposure to COVID-19 [22,31,32]. Mental health conditions can lead to impediments in the immune system, which make an individual more susceptible to COVID-19 and increase situations of greater exposure to COVID-19 [22,31,32]. This is particularly relevant to individuals experiencing homelessness, who are a vulnerable population at high risk for mental health conditions and must undergo COVID-19 testing to gain entrance to shelters [11,15,31-33].

Challenges to Health and Economic Distress

Those individuals who have challenges in having a place to stay/live and those with the interaction of DCI and getting needed medication were more likely to be symptomatic at the time of testing. These socioeconomic issues could be associated with these individuals being more vulnerable to exposures, leading to more chances of respiratory disease spread due to related aspects such as homelessness or not being able to afford health care such as medication. It was found that individuals who reported challenges in getting needed medicine or transportation, those who lived in distressed communities, and those with the interaction of living in a distressed community while having challenges in having a place to stay/live were less likely to be symptomatic at the time of testing. These associations with not having issues of getting needed medicine or transportation challenges to health could indicate there are fewer travel/access obstacles to the health of an individual as well as fewer people experiencing homelessness in these socioeconomic groups. This could indicate that individuals who are not impeded by these socioeconomic drivers are more likely to seek testing when becoming symptomatic. Coinciding with having no challenges to health, living in higher areas of greater economic distress was associated with lower odds of being symptomatic (Figure 1: pink areas). These findings are interesting because these components measure socioeconomic challenges at both the individual and community levels. These findings give insight into the behaviors of underserved communities that exist across West Virginia when compared to previous studies that look at population-level data and collection methods that would otherwise limit these underserved communities [15,17].

Limitations

This study has several limitations. First, data for the study comes from questionnaires that are self-reported by the individuals. Due to recall bias or social desirability bias, individuals may be misclassified according to symptomatic status or the presence of a potential predictor [34,35]. Next, many of these symptoms that individuals reported could also be present in the transmission of other pathogens [36]. However, we believe that this did not impact the validity of the study, as the goal was to better understand which factors were associated with the use of testing services in any individual who was symptomatic. Third, individuals who were symptomatic faced challenges to health, such as getting to a testing site or not knowing about available testing, and may not have sought testing. Fourth, the sample size does not indicate confirmed COVID-19 cases—only those who were symptomatic and seeking COVID-19 testing. Finally, the study population is only a subset of the total underserved areas of West Virginia, and some study variables had small sample representation or missing data.

Conclusions

Overall, this study of symptomatic factors associated with COVID-19 testing in West Virginia emphasized the urgent need to better understand barriers to testing. Despite limitations, this research addresses gaps in the current COVID-19 testing research. This is especially important in underserved areas experiencing disparities, such as the southwestern part of West Virginia (Figure 1). Critical to future public health policy creation is determining why individuals who are symptomatic in high-distress areas are less likely to seek free COVID-19 testing. While factors such as a lack of transportation are possible, there may be other reasons such as belief in the presence of ongoing SARS-CoV-2 transmission or belief in effective prevention (eg, vaccines or quarantine) or treatment.

Acknowledgments

Melanie Taylor, Triston Nutter, Caitlin Herdman, Raven Allen, Katherine Belcher, and Andrew Meyer of West Virginia Clinical and Translational Science Institute all provided research support. Research support was received from the National Institute of General Medical Sciences of the National Institutes of Health (NIH NIGMS) under award 2U54GM104942-07 for the West Virginia Clinical and Translational Science Institute. Additional support was provided by the National Institute on Minority Health and Health Disparities’ Rapid Acceleration of Diagnostics Among Underserved Populations (RADx-UP; 1U01MD017419-01) and NIH NIGMS RADx-UP (3U54GM104942-06S1). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Data Availability

The original data sets contain personal health information and small identifiable subgroups, and cannot be shared publicly. For questions about data availability, contact the corresponding author.

Conflicts of Interest

None declared.

  1. Manabe YC, Sharfstein JS, Armstrong K. The need for more and better testing for COVID-19. JAMA. Dec 1, 2020;324(21):2153-2154. [CrossRef] [Medline]
  2. Lauring AS, Tenforde MW, Chappell JD, et al. Clinical severity of, and effectiveness of mRNA vaccines against, COVID-19 from omicron, delta, and alpha SARS-CoV-2 variants in the United States: prospective observational study. BMJ. Mar 9, 2022;376:e069761. [CrossRef] [Medline]
  3. Thorne LG, Bouhaddou M, Reuschl AK, et al. Evolution of enhanced innate immune evasion by SARS-CoV-2. Nature. Feb 2022;602(7897):487-495. [CrossRef] [Medline]
  4. Caputo V, Calvino G, Strafella C, et al. Tracking the initial diffusion of SARS-CoV-2 omicron variant in Italy by RT-PCR and comparison with Alpha and Delta variants spreading. Diagnostics (Basel). Feb 11, 2022;12(2):467. [CrossRef] [Medline]
  5. Schulz C. State still tracking COVID-19, despite reduced testing. West Virginia Public Broadcasting. Jul 22, 2022. URL: https://wvpublic.org/state-still-tracking-covid-19-despite-reduced-testing/ [Accessed 2024-07-04]
  6. Kaufman BG, Whitaker R, Pink G, Holmes GM. Half of rural residents at high risk of serious illness due to COVID-19, creating stress on rural hospitals. J Rural Health. Sep 2020;36(4):584-590. [CrossRef] [Medline]
  7. Huttlinger K, Schaller-Ayers J, Lawson T. Health care in Appalachia: a population-based approach. Public Health Nurs. 2004;21(2):103-110. [CrossRef] [Medline]
  8. Price BS, Khodaverdi M, Halasz A, et al. Predicting increases in COVID-19 incidence to identify locations for targeted testing in West Virginia: a machine learning enhanced approach. PLoS One. Nov 3, 2021;16(11):e0259538. [CrossRef] [Medline]
  9. Hendricks B, Price BS, Dotson T, et al. If you build it, will they come? Is test site availability a root cause of geographic disparities in COVID-19 testing? Public Health. Mar 2023;216:21-26. [CrossRef] [Medline]
  10. Hendricks B, Paul R, Smith C, et al. Coronavirus testing disparities associated with community level deprivation, racial inequalities, and food insecurity in West Virginia. Ann Epidemiol. Jul 2021;59:44-49. [CrossRef] [Medline]
  11. Yang W, Zhang D, Peng L, Zhuge C, Hong L. Rational evaluation of various epidemic models based on the COVID-19 data of China. Epidemics. Dec 2021;37:100501. [CrossRef] [Medline]
  12. Aleta A, Martín-Corral D, Pastore Y Piontti A, et al. Modelling the impact of testing, contact tracing and household quarantine on second waves of COVID-19. Nat Hum Behav. Sep 2020;4(9):964-971. [CrossRef] [Medline]
  13. Tromberg BJ, Schwetz TA, Pérez-Stable EJ, et al. Rapid scaling up of COVID-19 diagnostic testing in the United States - the NIH RADx Initiative. N Engl J Med. Sep 10, 2020;383(11):1071-1077. [CrossRef] [Medline]
  14. Alvarez E, Bielska IA, Hopkins S, et al. Limitations of COVID-19 testing and case data for evidence-informed health policy and practice. Health Res Policy Syst. Jan 25, 2023;21(1):11. [CrossRef] [Medline]
  15. Graham MS, May A, Varsavsky T, et al. Knowledge barriers in a national symptomatic-COVID-19 testing programme. PLOS Glob Public Health. Jan 19, 2022;2(1):e0000028. [CrossRef] [Medline]
  16. Elliot AJ, Harcourt SE, Hughes HE, et al. The COVID-19 pandemic: a new challenge for syndromic surveillance. Epidemiol Infect. Jun 18, 2020;148:e122. [CrossRef] [Medline]
  17. Allen WE, Altae-Tran H, Briggs J, et al. Population-scale longitudinal mapping of COVID-19 symptoms, behaviour and testing. Nat Hum Behav. Sep 2020;4(9):972-982. [CrossRef] [Medline]
  18. Kirby JB, Yabroff KR. Rural-urban differences in access to primary care: beyond the usual source of care provider. Am J Prev Med. Jan 2020;58(1):89-96. [CrossRef] [Medline]
  19. Shea D, Stuart B, Vasey J, Nag S. Medicare physician referral patterns. Health Serv Res. Apr 1999;34(1 Pt 2):331-348. [Medline]
  20. Corbie G, D’Agostino EM, Knox S, et al. RADx-UP coordination and data collection: an infrastructure for COVID-19 testing disparities research. Am J Public Health. Nov 2022;112(S9):S858-S863. [CrossRef] [Medline]
  21. About RADx-UP. RADx-UP. URL: https://radx-up.org/about/ [Accessed 2024-07-04]
  22. Mody A, Pfeifauf K, Bradley C, et al. Understanding drivers of coronavirus disease 2019 (COVID-19) racial disparities: a population-level analysis of COVID-19 testing among black and white populations. Clin Infect Dis. Nov 2, 2021;73(9):e2921-e2931. [CrossRef] [Medline]
  23. Maharaj AS, Parker J, Hopkins JP, et al. The effect of seasonal respiratory virus transmission on syndromic surveillance for COVID-19 in Ontario, Canada. Lancet Infect Dis. May 2021;21(5):593-594. [CrossRef] [Medline]
  24. Leining LM, Short K, Erickson TA, et al. Syndromic surveillance among evacuees at a Houston “Megashelter” following Hurricane Harvey. Sustainability. May 16, 2022;14(10):6018. [CrossRef]
  25. Distressed Communities Index (DCI). Economic Innovation Group. URL: https://eig.org/issue-areas/distressed-communities-index-dci/ [Accessed 2024-07-11]
  26. Witrick B, Shi L, Mayo R, Hendricks B, Kalbaugh CA. The association between socioeconomic distress communities index and amputation among patients with peripheral artery disease. Front Cardiovasc Med. Nov 3, 2022;9:1021692. [CrossRef] [Medline]
  27. Hawkins RB, Charles EJ, Mehaffey JH. Socio-economic status and COVID-19-related cases and fatalities. Public Health. Dec 2020;189:129-134. [CrossRef] [Medline]
  28. What is a z-score? What is a p-value? ArcGIS. 2023. URL: https:/​/pro.​arcgis.com/​en/​pro-app/​latest/​tool-reference/​spatial-statistics/​what-is-a-z-score-what-is-a-p-value.​htm [Accessed 2024-07-04]
  29. Clark A, Jit M, Warren-Gash C, et al. Global, regional, and national estimates of the population at increased risk of severe COVID-19 due to underlying health conditions in 2020: a modelling study. Lancet Glob Health. Aug 2020;8(8):e1003-e1017. [CrossRef] [Medline]
  30. Adab P, Haroon S, O’Hara ME, Jordan RE. Comorbidities and COVID-19. BMJ. Jun 15, 2022;377:1431. [CrossRef] [Medline]
  31. The Lancet Infectious Diseases. The intersection of COVID-19 and mental health. Lancet Infect Dis. Nov 2020;20(11):1217. [CrossRef] [Medline]
  32. Marel C, Mills KL, Teesson M. Substance use, mental disorders and COVID-19: a volatile mix. Curr Opin Psychiatry. Jul 1, 2021;34(4):351-356. [CrossRef] [Medline]
  33. Ahillan T, Emmerson M, Swift B, et al. COVID-19 in the homeless population: a scoping review and meta-analysis examining differences in prevalence, presentation, vaccine hesitancy and government response in the first year of the pandemic. BMC Infect Dis. Mar 14, 2023;23(1):155. [CrossRef] [Medline]
  34. Fadnes LT, Taube A, Tylleskär T. How to identify information bias due to self-reporting in epidemiological research. Internet J Epidemiol. Jan 2009;7(2):28-38. [CrossRef]
  35. Althubaiti A. Information bias in health research: definition, pitfalls, and adjustment methods. J Multidiscip Healthc. May 4, 2016;9:211-217. [CrossRef] [Medline]
  36. Larsen JR, Martin MR, Martin JD, Kuhn P, Hicks JB. Modeling the onset of symptoms of COVID-19. Front Public Health. Aug 13, 2020;8:473. [CrossRef] [Medline]


aOR: adjusted odds ratio
CDE: common data element
DCI: Distressed Communities Index
RADx-UP: Rapid Acceleration of Diagnostics for Underserved Populations
SOAR: Solutions Oriented Addiction Response


Edited by Amaryllis Mavragani; submitted 14.09.23; peer-reviewed by Ranganathan Chandrasekaran, Supharerk Thawillarp; final revised version received 03.06.24; accepted 06.06.24; published 18.07.24.

Copyright

© Timothy Dotson, Brad Price, Brian Witrick, Sherri Davis, Emily Kemper, Stacey Whanger, Sally Hodder, Brian Hendricks. Originally published in JMIR Public Health and Surveillance (https://publichealth.jmir.org), 18.7.2024.

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