Assessment of Utility of accelerateIQ in the Care of Patients Participating in a Pulmonary Rehabilitation Program

Terminated

• Conditions: COPD; Pulmonary Rehabilitation

• Registration Number: NCT03879291
• Lead Sponsor: Karen Larimer

Brief Summary

The proposed study seeks to assess the performance of continuous biosensor data and machine learning analytics in assessment of health patient status in a pulmonary rehabilitation program.

It is hypothesized that using continuous physiologic biosensor data and machine learning analytics to detect changes in physiology may play a role in managing patients in the pulmonary rehabilitation setting.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-01-09
• Study First Submitted: 2019-03-14
• Study First Submitted QC: 2019-03-15
• Study First Posted: 2019-03-18
• Primary Completion: 2019-12-30
• Study Completion: 2019-12-30
• Status Verified: 2020-03
• Last Update Submitted: 2020-03-12
• Last Update Posted: 2020-03-16

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

• Male or female, at least 40 years of age;
• Diagnosis of Chronic Obstructive Pulmonary Disease (COPD);
• Enrolled in the study site's 12-week pulmonary rehabilitation program;
• Capable of completing a 6-minute walk test;
• Willing and able to comply with scheduled protocol procedures and follow up;
• Signed and dated informed consent and HIPAA materials indicating that the patient has agreed to participate in this study and has been informed of all pertinent aspects of the trial.

Exclusion Criteria

• Patient has cognitive or physical limitations that, in the opinion of the investigator, limit the patient's ability to utilize the System as instructed;
• Patient is actively enrolled in another clinical investigation that, in the opinion of the investigator, interferes with or compromises either that patient's ability to participation in this study or the ability for the study to generate results;
• Patients who have implanted defibrillators or pacemakers;
• Patient is allergic to hydrocolloid adhesive;
• Patient does not speak English.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Clinical Utility	90 days	Correlation of reported health events with the multivariate change index

Trial Locations

Locations (1)

NorthShore University Health System; 🇺🇸 Evanston, Illinois, United States