Breathing without drugs: biofeedback trial aims to ease persistent shortness of breath
NCT ID NCT05973513
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This UCLA study tests whether biofeedback—a technique that teaches control over heart rate, breathing, and body temperature—can relieve shortness of breath in people who haven't gotten better with inhalers or pulmonary rehab. Twenty-five adults aged 18–60 with ongoing respiratory symptoms will attend six sessions. The goal is to see if symptoms, mood, sleep, and quality of life improve.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- biofeedback (heart-rate variability training, relaxation, temperature control)
- What this could lead to
- If it works, this could offer a non-drug way to manage persistent breathing problems and improve quality of life.
- What could go wrong
- This is a small, early-stage trial with only 25 people and no comparison group, so results may not apply widely. It also relies on self-reported improvements.
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.
- Participants
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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2021
- Expected to finish
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Jul 2028
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.
Who is studied
(1) participants must be between 18-60; (2) English speaking; (3) must have least one respiratory sx and have received care from a pulmonologist for this sx
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. participants must be between 18-60 2. English speaking 3. must have least one respiratory sx and have received care from a pulmonologist for this sx Exclusion Criteria: severe psychopathology (e.g., psychosis, active suicidality, moderate to severe intellectual impairment).
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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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Natacha Emerson
Los Angeles, California, 90095, United States