RecruitingRecruiting
The Increase of Lung Capacity Using the Lung Master (Pulmonary Exerciser)
NCT06524856 · University of Nebraska
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
Shortness of breath,or dyspnea, occurs when the lungs do not receive enough oxygen leading to discomfort when breathing. This occurs in a quarter of individuals seen in an outpatient setting. Several factors can relate to breathlessness, including lung disorders, heart conditions, or stress. Patients with breathlessness often experience physical limitations in their daily activities. Various treatments for dyspnea are available, however, chronic breathlessness syndrome, such as asthma or chronic obstructive pulmonary disease (COPD), still can persist even when treatment is available.
The Lung Master (Pulmonary Exerciser) is a breathing device used for the respiratory treatment and rehabilitation of chronic breathlessness syndrome. The Lung Master increases resistance during inhalation and exhalation, which works to strengthen the respiratory muscle and improve overall lung function. Therefore, this study will focus on determining how the Lung Master increases lung capacity in healthy individuals. The device is considered investigational and has not been approved by the FDA.
Two groups of healthy participants will be sought for the study: ages 19 to 35 and ages 65 and above. Each participant will have two in-office study visits approximately one month apart. Each visit will take around one to two hours to complete. At the visits, a breathing test called a spirometry test will be done. During the one month interim, the study device will be used at home and the use recorded in a diary. The device must be used least once every day, either in the morning or in the evening for 5 to 20 minutes. You will be contacted after two weeks, and then return the device at the second study visit.
Eligibility criteria
Inclusion Criteria:
* able to complete the at home portion of the study daily
* fall within the age ranges: 19-35 and above 65 years old
Exclusion Criteria:
* any respiratory or chronic conditions
Study design
Enrollment target: 20 participants
Allocation: na
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2024-10-01
Estimated completion: 2027-03
Last updated: 2026-03-11
Interventions
Device: Lung Master (Pulmonary Exerciser)
Primary outcomes
- • Inspiratory Capacity (baseline and after one month of device use)
- • Tidal Volume (baseline and after one month of device use)
Sponsor
University of Nebraska · other
Contacts & investigators
ContactAnn Nguyen, BS · contact · annnguyen@unomaha.edu · 402-554-2383
ContactJania Williams, MS · contact · janiawilliams@unomaha.edu · 404-895-7610
InvestigatorFarahnaz Fallah Tafti, PhD · principal_investigator, University of Nebraska
All locations (1)
Biomechanics Research BuildingRecruiting
Omaha, Nebraska, United States