SEEKING COVID POSITIVE VOLUNTEERS Long-term Impact of the Novel Coronavirus 19 (COVID-19) on Cardiopulmonary Health in Women

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  • participants needed
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Updated on 19 February 2024

Summary

The purpose of this study is to investigate possible long-term changes in heart and lung health associated with COVID-19. 
 
Your participation may help researchers to better understand how COVID-19 impacts cardiovascular and pulmonary health of women.

Description

This study will take a minimum of 12 months to complete and involves 6 in-person visits (2 study visits at baseline, 6 months, and 12 months later). 
 
Study participants will be asked to do the following:
  • Complete some questionnaires
  • Perform breathing tests
  • Do an exercise treadmill test
  • Have physical measurements taken (e.g., height, weight, heart rate)
Participants will receive a $50 gift card after the second visit at baseline, 6 months, and 12 months later, for a total of $150.
 
 
 
All study visits are conducted at the Indiana University School of Public Health in Bloomington.
 
 
 Study Visit 1:
  • Complete a questionnaire
  • 6-minute walk test
  • Breath analysis
  • Pulmonary function tes
  • DXA scan
  • BIA scan

Study Visit 2:
  • Complete a 24-hour diet log
  • Blood and urine collection
  • Questionnaires
  • Submaximal walking test

FAQ

 Study Visit 1:
  • Complete a questionnaire
  • 6-minute walk test
  • Breath analysis
  • Pulmonary function tes
  • DXA scan
  • BIA scan

Study Visit 2:
  • Complete a 24-hour diet log
  • Blood and urine collection
  • Questionnaires
  • Submaximal walking test

Details
Condition COVID-19,COVID19,COVID 19,COVID,coronavirus,corona virus,corona,virus,cardiopulmonary,heart,lungs
Age 50years - 75years
Clinical Study Identifier2004439367
Last Modified on19 February 2024

Eligibility

How to participate?

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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