MoblO2 for activity-related oxygen delivery in COPD and ILD

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center, cross-over study where adults with COPD or ILD who use oxygen for exertion will wear their usual oxygen setup and participate in two weeks of activity with MoblO2. In one week, the MoblO2 device collects data without changing oxygen flow; in the other week, it automatically controls O2 flow during exertion. The trial uses an initial O2 titration to determine baseline needs and compares outcomes with and without flow control. An activity monitor will track physical activity and symptoms to gauge impact on oxygen use and daily function.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Previously-diagnosed COPD or chronic interstitial lung disease Prescribed O2 for use with exertion at least 1 month prior to enrollment Age 25 years old or greater Self-reported stable symptoms and stable oxygen needs for at least 2 weeks Consent to using compressed gas tanks to deliver O2 during the 2-week study period

Exclusion Criteria:

Active angina Musculoskeletal disease that precludes physical activity Need for O2 at rest Patient needing more than 10 L/min continuous flow with exertion on O2 screen Patient prescribed 10L/min continuous flow (or more) by their prescribing practitioner

Where it's running

• National Jewish Health
  Denver, Colorado, United States Recruiting

Study contacts

• Study coordinator: Jeff Swigris, DO, MS
• Email: swigrisj@njhealth.org
• Phone: 303-398-1790

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.