Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05938738

PEP-buddy in COPD: Effect on Dyspnea Severity and Mechanism of Action

A Portable Dyspnea Relief Device for Episodic Breathlessness in COPD (PEP-buddy): Effect on Dyspnea Severity and Mechanism of Action

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
25 (estimated)
Sponsor
University Medical Center Groningen · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

Chronic dyspnea is the most characteristic symptom of patients with Chronic Obstructive Pulmonary Disease (COPD), with intermittent increases during exercise and other events.Despite optimal standard therapy, episodic dyspnea is a common occurrence in COPD. Recently, the PEP buddy was developed which is an easy-to use, hands-free device that generates positive expiratory pressure (PEP). Although currently the available evidence is limited, it indicates that utilizing the PEP-buddy can result in enhancements in dyspnea during exertion, exertional desaturation and overall quality of life. More research is needed to evaluate the effectiveness of this device and the long term usability, as well as getting more insight in the mechanism of action. Therefore, the aim of our study is to explore the potential of this device for patients with COPD and episodic breathlessness.

Conditions

Interventions

TypeNameDescription
DEVICEPEP-buddyPEP-buddy

Timeline

Start date
2024-01-31
Primary completion
2025-12-31
Completion
2025-12-31
First posted
2023-07-10
Last updated
2025-03-27

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT05938738. Inclusion in this directory is not an endorsement.