No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
40 – 89
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
VA Office of Research and Development · Federal
Who this trial is looking for
This trial is looking for Veterans with COPD who are going to Pulmonary Rehabilitation. Participants will use a special device that might help with breathing and exercise during their treatment.
Are You a Good Fit for This Trial?
You may be able to join if
I am a Veteran
I am referred to Pulmonary Rehabilitation for COPD
My FEV1 is less than 80% predicted
I can exercise with 4L/m of oxygen through a nasal cannula
You may not be able to join if
I have another lung disease that affects my breathing
I cannot perform study procedures or use the PEP Buddy device
I have a lung disease caused by aspiration or neurological issues
My life expectancy is less than 1 year
I have a planned surgery that requires a long recovery
I have a serious cancer beyond Stage I or non-melanoma skin cancer
I have memory loss shown by MOCA testing
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
In this study, the investigators will test Veterans with COPD in Pulmonary Rehabilitation. Between two groups, the investigators will give one group a device that assists with breathing and symptoms and the other receives a 'sham' device which does not provide these benefits. The investigators will test to see if the symptoms and exercise capacity of the group who receives this device improves fas…
In this study, the investigators will test Veterans with COPD in Pulmonary Rehabilitation. Between two groups, the investigators will give one group a device that assists with breathing and symptoms and the other receives a 'sham' device which does not provide these benefits. The investigators will test to see if the symptoms and exercise capacity of the group who receives this device improves faster in Pulmonary Rehabilitation and has longer lasting benefits after the end of Pulmonary Rehabilitation.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* Veteran
* Referral to Pulmonary Rehabilitation for COPD
* FEV1 \<80% predicted
* Participants must be able to exercise on 4L/m nasal cannula O2
Exclusion Criteria:
* Those deemed by the study personnel to have a lung disease other than COPD impacting their daily dyspnea
* Th…
Inclusion Criteria:
* Veteran
* Referral to Pulmonary Rehabilitation for COPD
* FEV1 \<80% predicted
* Participants must be able to exercise on 4L/m nasal cannula O2
Exclusion Criteria:
* Those deemed by the study personnel to have a lung disease other than COPD impacting their daily dyspnea
* Those that are unable to perform study procedures or are unwilling or unable to use PEP Buddy
* Those that have a component of lung disease driven by aspiration or neurological conditions affecting the face or oropharynx
* Those with a life expectancy of \<1 year
* Those with a known surgical intervention that will require a prolonged recovery in the year after enrollment
* Those with a malignancy beyond Stage I or non-melanoma skin cancer
* Those shown shown to have memory loss of MOCA testing
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