Can exercise help black women breathe easier? new study aims to find out
NCT ID NCT05726487
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a 24-week lifestyle physical activity program designed for Black women with asthma. Participants are randomly assigned to either the activity program (group sessions, activity tracking, and text support) or an asthma education control group. The goal is to see if the program improves asthma control and quality of life, and whether any benefits last for an additional 24 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lifestyle physical activity program (group sessions, self-monitoring, text support)
- What this could lead to
- If it works, this could provide an effective, non-drug way to improve asthma control and quality of life for Black women with asthma.
- What could go wrong
- This is an early efficacy study, not a large phase 3 trial. The intervention may not produce lasting improvements, and results may not apply to other groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 224 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Self-identify as female and Black or African-American * Age \>/= 18 * Physician-diagnosed persistent asthma that is sub-optimally controlled based on Asthma Control Test (ACT \< 20) OR history in the past year of an asthma exacerbation (a need for systemic corticosteroids or hospital admission or emergency treatment for worsening asthma) * Willing to enroll and provide written-informed consent * Willing to be randomly assigned to treatment or control group * Low- active: engages in less than 150 minutes per week of moderate-to- vigorous physical activity * Has a smartphone and texts every day or almost everyday Exclusion Criteria: * Plans to relocate outside of the Chicagoland area during the study period * Unable to ambulate without the use of a wheelchair or scooter * Diagnosis of COPD (emphysema or chronic bronchitis) suggested by patient report of doctor diagnosis or smoking history (≥ 20 pack years) * Current tobacco smoker * A contraindication to exercise as indicated by the Physical Activity Readiness Questionnaire unless written permission by a health care provider * Significant medical (e.g., unstable heart disease, uncontrolled high blood pressure, active cancer treatment in past 1 year, end-stage organ failure) or psychiatric (e.g., active bipolar disorder, psychosis) comorbidities * Participation in another physical activity or asthma research program * Asthma exacerbation, defined by an urgent care visit for asthma in the last 4 weeks, or need for acute course of systemic corticosteroids for asthma in the last 4 weeks * Family/household member of another study participant or staff member * Inability to speak, read or understand English * Investigator discretion for safety or protocol adherence reasons * Unable or unwilling to provide complete accelerometry data at the baseline assessment after two opportunities to wear the monitor
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Chicago
Chicago, Illinois, 60637, United States
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University of Illinois Chicago
Chicago, Illinois, 60607, United States
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