Respiration Rate Monitoring in COPD Patients

Completed · Not applicable

Conditions studied: Pulmonary Disease, Chronic Obstructive

In brief

Assess the feasibility of using remote respiration rate monitoring as a component of home care, how respiration rate data may be used in combination with other data to potentially improve response to symptoms, and to generate data to inform the endpoints and effect sizes of future studies.

Key facts

Study ID

NCT03030313

Run by

ResMed

People needed

50

Starts

2016-12-01

Expected to finish

2017-07-26

Last updated by the study team

2017-11-17

Who can join

Age: 35 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or females age ≥35 years old
• Documented diagnosis of moderate to very severe COPD (GOLD Level II-IV)
• Weight ≥35 kg
• Currently using the COPD Co-PILOT application (at least 3 months with 70% compliance)
• Must be able to read and understand English and consent for themselves

You may not qualify if…

• Currently using any form of non-invasive positive airway pressure ventilation
• Diagnosis of significant heart failure (NYHA Class III or IV)
• Cognitive impairment (determined by physician) that will make it hard to follow instructions regarding device usage
• BMI ≥45.5
• Residing in hospice care, Skilled Nursing Facilities or Long Term Acute Care facilities
• Currently using a wearable drug infusion pump to deliver medication
• Planned procedures at time of enrollment that will occur within timeframe of study and require hospitalization etc.
• Declines to participate at any time.
• In the opinion of the Investigator, may be non-compliant with study schedules or procedures
• No cellular coverage at their primary residence

Where it is running

• HGE Health Care Solutions — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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