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Deep Functional Phenotyping of the ALA Lung Health Cohort

Johns Hopkins University · with National Heart, Lung, and Blood Institute (NHLBI), American Lung Association · NCT06177717

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 25–35 · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
1000
US sites recruiting
12
Study start
February 12, 2024
Record last updated
July 17, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The goal of this observational study is to learn about lung structure and function in a group of 1000 healthy people aged 25 to 35. The main questions it aims to answer are whether people's bodies, environment, and general lung health are associated with:

  • the structure of the participants lungs' airways,
  • the structure of blood vessels in the participants lungs and heart, and
  • the participants lungs' ability to exchange gases.

Participants will take four different lung function tests to measure lung function, including:

  • air movement in the lungs (oscillometry)
  • lung size (slow vital capacity (SVC) and functional residual capacity (FRC)
  • gas transfer in the lungs (diffusing capacity for carbon monoxide (DLCO).

Conditions: Lung Diseases

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

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 months prior 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 know the whereabouts and vital status of the participant

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 beta agonist (ICS/LABA) or high dose inhaled corticosteroid [ICS] or add-on long-acting muscarinic antagonist (LAMA); Medium dose = >250 fluticasone, propionate =100 fluticasone furoate, >200 beclomethasone, >400 budesonide, >220 mometasone). The investigators will accept low-dose ICS/LABA or medium dose ICS.

OR

  • 3 or more unscheduled healthcare visits (provider/urgent care/ER) for asthma in the 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 to chronic 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 heart disease)
  • 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 by participating in the study (e.g., serious respiratory illness requiring antibiotics or steroids or severe fever at the time of the study visit).
  • Institutionalization

Recruiting US locations

  • University of Alabama

    Birmingham, AL 35294

    Site contact: Michelle Williams · 205-934-6683 · michellewilliams@uabmc.edu

  • University of California, Los Angeles

    Los Angeles, CA 90095

    Site contact: Tiffany Bina · 310-206-1629 · tbina@mednet.ucla.edu

  • National Jewish Health

    Denver, CO 80206

    Site contact: Madeleine Caruso · 303-398-1443 · CARUSOM@NJHEALTH.ORG

  • Nemours Children's Jacksonville

    Jacksonville, FL 32207

    Site contact: Julia Krutov · 904-697-3925 · biomedicalresearch@nemours.org

  • Northwestern University

    Chicago, IL 60611

    Site contact: Shafic Kakooza · 312-503-6378 · lhc@northwestern.edu

  • University of Kansas

    Kansas City, KS 66103

    Site contact: John McLean · 913-574-0176 · jmclean@kumc.edu

  • Johns Hopkins University

    Baltimore, MD 21218

    Site contact: Molly Lauver · 410-550-2863 · mlauver3@jhmi.edu

  • University of Michigan

    Ann Arbor, MI 48109

    Site contact: Wendy Warshal · 734-232-2841 · warshal@med.umich.edu

  • Duke University

    Durham, NC 27710

    Site contact: Kaitlin Foy · 919-479-0861 · DukeAirwayResearch@duke.edu

  • Wake Forest School of Medicine

    Winston-Salem, NC 27104

    Site contact: Abby Paust · 336-713-8550 · apaust@wakehealth.edu

  • University of Pittsburgh - Emphysema/COPD Research Center

    Pittsburgh, PA 15213

    Site contact: Casey Rapoza · 412-692-4876 · rapozaca@upmc.edu

  • University of Vermont

    Burlington, VT 05446

    Site contact: Olivia Garrow · 802-847-2160 · olivia.johnson@uvmhealth.org

Study contacts (from the official record)

  • Meredith McCormack, MD · 410-955-3467 · mmccor16@jhmi.edu
  • Alexis Rea, MPH · 443-287-8496 · area5@jhu.edu
Deep Functional Phenotyping of the ALA Lung Health Cohort (NCT06177717) | Bored Studies