Respiration Rate Monitoring in COPD Patients

Not Applicable

Completed

• Conditions: Pulmonary Disease, Chronic Obstructive
• Interventions: Device: Reassure Non-Contact Respiration Monitor

• Registration Number: NCT03030313
• Lead Sponsor: ResMed

Brief Summary

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.

Detailed Description

The research question is whether monitoring of respiration rates and variability can be helpful in management of COPD patients in conjunction with or separately from self-reported symptom scores using the COPD Co-PILOT application. Current techniques (such as patient's self-reported symptoms) have limited sensitivity and specificity with regard to predicting decompensation. Measurement of respiration parameters and the variability of the parameters may detect worsening COPD. Changes in respiration patterns may occur sufficiently far in advance of decompensation (e.g. \>5 days prior to patient symptoms) such that it would allow an opportunity for earlier intervention with medical assessment and current therapeutic approaches.

The specific primary aim includes evaluation of the correlation of respiration rate parameters to indicators of healthcare utilization including drug changes, office or ER visits, hospitalization, or other clinical interventions. Secondary aims include evaluation of (i) the sensitivity and specificity of respiration rate monitoring results to predict COPD worsening requiring medical intervention, (ii) the sensitivity and specificity of respiration rate monitoring results in conjunction with COPD Co-PILOT scores or components to predict COPD worsening requiring medical intervention, and the correlation of respiration rate parameters to episode duration as defined by number of days from COPD Co-PILOT Score \>1 to resolution (COPD Co-PILOT Score \<1 for 7 consecutive days).

Study Timeline

• Study First Submitted: 2016-11-18
• Study Start: 2016-12-01
• Study First Submitted QC: 2017-01-20
• Study First Posted: 2017-01-25
• Primary Completion: 2017-07-26
• Study Completion: 2017-07-26
• Status Verified: 2017-11
• Last Update Submitted: 2017-11-14
• Last Update Posted: 2017-11-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• 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

Exclusion Criteria

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Respiration rate monitoring	Reassure Non-Contact Respiration Monitor	Reassure Non-Contact Respiration Monitor

Primary Outcome Measures

Name	Time	Method
Correlation of Respiration Rate to Indicators of Healthcare Utilization	12 weeks	Indicators of healthcare utilization include change in medications for COPD, number of office or ER visits, number of hospitalizations.

Secondary Outcome Measures

Name	Time	Method
Sensitivity and Specificity of Respiration Rate to Predict COPD Worsening	Baseline to 12 weeks
Sensitivity and Specificity of Respiration Rate in Conjunction with COPD Co-PILOT Scores to Predict COPD Worsening	12 weeks
Correlation of Respiration Rate to COPD Episode Duration	12 weeks	Episode duration is defined by number of days from COPD Co-PILOT Score \>1 to resolution (COPD Co-PILOT Score \<1 for 7 consecutive days)

Trial Locations

Locations (1)

HGE Health Care Solutions; 🇺🇸 Philadelphia, Pennsylvania, United States