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Risk Underlying Rural Areas Longitudinal Cohort Study (RURAL) Heart and Lung Study

RURAL Heart and Lung Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05006729
Acronym
RURAL
Enrollment
4600
Registered
2021-08-16
Start date
2021-01-15
Completion date
2031-04-01
Last updated
2026-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Diseases, Pulmonary Disease, Rural Health

Keywords

Risk factors for heart disease, Risk factors for lung disease, Psychosocial factors, Familial factors, Economic factors, Mobile examination unit (MEU), Alabama, Kentucky, Louisiana, Mississippi

Brief summary

The University of Texas Health Science Center at San Antonio (UTHSCSA) will serve as the site for the RURAL Study Coordinating Center, led by PI Vasan Ramachandran, MD. The primary function of the Study Coordinating Center (SCC) is to serve as an administrative liaison between all of the RURAL study's cores. The SCC schedules, facilitates, and hosts, all RURAL meetings including preparation for Observational Study Monitoring Board (OSMB) meetings, and maintains direct communication with the study's program officers at NHLBI. The SCC monitors the overall progress of RURAL and keeps all RURAL cores abreast of study updates through meetings, emails, newsletters. It also maintains the official RURAL website and serves as an administrator for investigators seeking to collaborate with RURAL through the submission of Ancillary Studies. The SCC will have no direct interaction with any participants, nor will it have access to identifiable data.

Detailed description

The Risk Underlying Rural Areas Longitudinal (RURAL) Cohort is a health research project that plans to enroll approximately 4,600 adults in ten rural counties throughout Alabama (AL), Kentucky (KY), Louisiana (LA), and Mississippi (MS). The ten specific counties are: Dallas County, AL; Wilcox County, AL; Boyle County, KY; Perry County, KY; Garrard County, KY; Breathitt County, KY; Assumption Parish, LA; Franklin Parish, LA; Oktibbeha County, MS; and Panola County, MS. The study will help to better understand health and disease in these rural areas. The information gathered in this study will help build future health programs to improve the health of local people in your community, which may promote healthier lives. Several different aspects of the participants' health will be examined including heart and lung function. Broad goals of the RURAL Cohort Study include: * Identifying the frequency of and risk factors for heart and lung diseases in the RURAL communities * Identifying unique factors contributing to health disorders in these communities - including psychosocial, economic, and familial factors - and how they interact together * Identifying potential solutions by examining differences between higher and lower risk rural counties Findings from the RURAL study will inform health care providers, participants, researchers and the community regarding the frequency, burden, determinants, and prognosis of heart, lung, blood, and sleep diseases in the rural South, provide new knowledge that is critical for rural implementation science, and set the stage for collaborative opportunities for a wider community of scientists. Participants in the RURAL Study will receive information on different areas of their health, including their heart and lungs. Investigators will visit participants in their communities to complete a research exam about heart and lung health. Participants will attend an in-person exam at the RURAL study mobile exam vehicle. On the mobile exam unit participants will also receive a Fitbit \[activity tracker\] device and a RURAL cell phone app that will be used to collect information about their health and lifestyle. Participants will receive results from their research exam, which they can also share with their doctor. The RURAL Study team will refer participants to a health center if there are immediate health concerns found during the research exam. The RURAL Study follows all HIPAA rules and regulations, in addition to the NIH and institutional guidelines, for the protection of all research participants. No information from the study that could identify a participant will be publicly shared. The RURAL study team will track participants' physical activity using the provided Fitbit device. The RURAL health team will also ask questions about overall health and lifestyle through the RURAL cell phone app. Participants will receive a kit to measure environmental and health factors in your home. The visit in the mobile exam vehicle will take about 3 hours and will include: * Vital signs including height and weight * Blood draw * Interviews and surveys asking about lifestyle and health history * Tests related to heart, lung, and blood vessel health

Interventions

None listed

Sponsors

The University of Texas Health Science Center at San Antonio
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
25 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* Be a resident of specific counties in Alabama, Kentucky, Louisiana, and Mississippi * Have resided in the specific county for the past two years and plan to reside at the residence for the next two years * Speak English or Spanish

Exclusion criteria

* Currently incarcerated or institutionalized * Currently in hospice care with a terminal illness and less than 6 month life expectancy * Being actively treated for cancer

Design outcomes

Primary

MeasureTime frame
Risk factors for lung disease in rural areas5 years
Risk factors for heart disease in rural areas5 years

Secondary

MeasureTime frame
Pulmonary function5 years
Heart function5 years

Countries

United States

Contacts

STUDY_DIRECTORVasan Ramachandran, MD

The University of Texas Health Science Center at San Antonio

PRINCIPAL_INVESTIGATORSuzanne Judd, PhD

University of Alabama at Birmingham

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 27, 2026