University of Michigan
Ann Arbor, Michigan, 48109, United States
Location status: Recruiting
Location contact
Gretchen Bautisita
CONTACT
MeiLan Han, MD, MS
PRINCIPAL_INVESTIGATOR
Stacey Anderson, MPH
CONTACT
NCT Number: NCT07482475
The purpose of this study is to obtain new knowledge regarding screening for COPD. This study will use a participant's cancer screening CT scans performed as part of routine health care among current and former smokers at risk for COPD to identify participants who have had a spirometry or will have a spirometry test as part of the study to verify COPD status.
Interested in participating?
Request Info50 year–80 year
All sexes
Observational
Ann Arbor, Michigan, 48109, United States
Location status: Recruiting
Gretchen Bautisita
CONTACT
MeiLan Han, MD, MS
PRINCIPAL_INVESTIGATOR
Stacey Anderson, MPH
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Current (i.e. at the time of the visit) GINA Step 4 or higher therapy (medium dose ICS/LABA or high dose ICS or add-on 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
Additional temporal exclusion criteria are as follows:
Time frame: Baseline
All participants in this study must have had a previous lung cancer screening CT scan as part of their normal medical care within one year of enrolling in this study. These pre-enrollment scans will be evaluated to determine how many scans that had been intended to identify lung cancer also indicate COPD.
Time frame: Baseline
Percentage of participants who meet spirometric criteria for COPD and have >1% LAA on lung cancer screening CT scan.
Time frame: Baseline
Participants will report how they experience their pulmonary health using the COPD Assessment Test (CAT) survey. The CAT is comprised of 8 questions which are each rated on a scale of 0-5, with 0 indicating no symptoms and 5 indicating worst symptoms. Ratings are then summed to generate a total score, between 0-40, with 40 indicating worst symptoms.
The investigators will utilize data from the COPD Assessment Test (CAT) to describe and gain a deeper understanding of participants' symptom and exacerbation burden within this study population.
Time frame: Baseline
Participants will be categorized into one of four GOLD categories based on their FEV1 values determined by a Pulmonary Function Test (PFT). If participants have had a PFT within the previous year, data from that test will be used. Otherwise, participants will be given a PFT during the study.
GOLD I (Mild COPD) = FEV1 >= 80% GOLD II (Moderate COPD) = 50% <= FEV1 < 80% GOLD III (Severe COPD) = 30% <= FEV1 < 50% GOLD IV (Very Severe COPD) = FEV1 < 30%
University of Michigan
Other
Acronym: MAP2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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