← Back to Clinical Trials
Recruiting NCT06524856

The Increase of Lung Capacity Using the Lung Master (Pulmonary Exerciser)

Trial Parameters

Condition Dyspnea
Sponsor University of Nebraska
Study Type INTERVENTIONAL
Phase N/A
Enrollment 20
Sex ALL
Min Age 19 Years
Max Age N/A
Start Date 2024-10-01
Completion 2027-03
Interventions
Lung Master (Pulmonary Exerciser)

Brief Summary

Investigators are studying how a device called The Lung Master device can help people breathe better. The investigational device increases the amount of air our lungs can hold, which is important for overall lung health. The Lung Master is not approved by the FDA. The study has two visits approximately one month apart. In the first visit participants will take a spirometry test, particularly forced vital capacity (FVC), to measure volume change in the lungs. Participants will take the investigational device home to use daily, either in the morning or evening. Use will be recorded in a diary. After one month, participants will return for another spirometry test. Each study visit will take about one to two hours to complete.

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

Related Trials