Phase
Condition
N/ATreatment
N/AClinical Study ID
Ages 25-35 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 25-35 years at the time of the baseline examination
Able to read and understand English or Spanish
Has a social security number
Resident (citizen or non-citizen) of the United States (US) for at least 12 monthsprior to examination.
Note: Individuals who are residents of the US who have temporarily spent time living outside of the US during the last 12 months (e.g., student exchange program, military posting) are eligible for participation.
- Willing to provide contact information for at least 2 proxies who are likely to knowthe whereabouts and vital status of the participant
Exclusion
Exclusion Criteria:
- Severe asthma, which is defined as any of the following:
Current (i.e. at the time of the visit) Global Initiative for Asthma (GINA)Step 4 or higher therapy (medium dose inhaled corticosteroid/long-acting betaagonist (ICS/LABA) or high dose inhaled corticosteroid [ICS] or add-onlong-acting muscarinic antagonist (LAMA); Medium dose = >250 fluticasone,propionate =100 fluticasone furoate, >200 beclomethasone, >400 budesonide, >220mometasone). The investigators will accept low-dose ICS/LABA or medium doseICS. OR
3 or more unscheduled healthcare visits (provider/urgent care/ER) for asthma inthe past 12 months OR
One asthma hospitalization in the past 12 months
History of any chronic lung disease other than asthma including but not limited tochronic obstructive pulmonary disease (COPD), cystic fibrosis, pulmonary fibrosis,pulmonary hypertension
Current pregnancy
History of cancer other than non-melanoma skin cancer
Diagnosed cardiovascular diseases (i.e., congenital heart disease, coronary heartdisease)
Inability to comply with study procedures, including
Inability or unwillingness to provide informed consent
Inability to perform study measurements
Inability to be contacted by phone (via calls and/or text messaging) or email
Any condition in the opinion of the physician that puts the participant at risk byparticipating in the study (e.g., serious respiratory illness requiring antibioticsor steroids or severe fever at the time of the study visit).
Institutionalization
Study Design
Study Description
Connect with a study center
University of Alabama
Birmingham, Alabama 35294
United StatesActive - Recruiting
University of California, Los Angeles
Los Angeles, California 90095
United StatesSite Not Available
National Jewish Health
Denver, Colorado 80206
United StatesActive - Recruiting
Nemours Children's Jacksonville
Jacksonville, Florida 32207
United StatesActive - Recruiting
Northwestern University
Chicago, Illinois 60611
United StatesActive - Recruiting
University of Kansas
Kansas City, Kansas 66103
United StatesActive - Recruiting
Johns Hopkins University
Baltimore, Maryland 21218
United StatesActive - Recruiting
University of Michigan
Ann Arbor, Michigan 48109
United StatesActive - Recruiting
Duke University
Durham, North Carolina 27710
United StatesActive - Recruiting
Wake Forest School of Medicine
Winston-Salem, North Carolina 27104
United StatesActive - Recruiting
University of Pittsburgh - Emphysema/COPD Research Center
Pittsburgh, Pennsylvania 15213
United StatesActive - Recruiting
University of Vermont
Burlington, Vermont 05446
United StatesActive - Recruiting
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