Actively Recruiting

Age: 25Years - 64Years
All Genders
Healthy Volunteers
NCT05006729

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

Led by The University of Texas Health Science Center at San Antonio · Updated on 2025-05-16

4600

Participants Needed

1

Research Sites

271 weeks

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center at San Antonio

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 25Years - 64Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Alabama

Birmingham, Alabama, United States, 35294

Actively Recruiting

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Research Team

V

Vasan Ramachandran, MD

CONTACT

R

Rachael Langey, BS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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