Skip to main content
Clinical Trials/NCT02999685
NCT02999685
Completed
Not Applicable

Home-based Health Management of COPD Patients

Mayo Clinic1 site in 1 country154 target enrollmentSeptember 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Mayo Clinic
Enrollment
154
Locations
1
Primary Endpoint
Quality of Life: Chronic Respiratory Questionaire
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Regular physical activity has been found to be important in maintaining health and well-being in people with COPD. The purpose of this study is to test new technology and health coaching aimed to help people with COPD become more physically active in their daily lives.

Detailed Description

This study consists of a home-based pulmonary rehabilitation system. The system consists of a tablet computer, pulse oximeter, activity monitor and weekly telephone health coach calls. The rehabilitation period lasts 8 weeks. This is a randomized trial with two groups. Group A will complete the study activities during the first 8 weeks of the study followed by a period of observation. Group B will complete 8 weeks of observation followed by 8 weeks of rehabilitation.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
June 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Roberto P. Benzo

M.D.

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • • Men and women age 40 years and older
  • Current or former smoker of at least 10 pack-years
  • Diagnosis of Global Initiative for Chronic Lung Disease (GOLD) stage II, III or IV COPD as documented by pulmonary function
  • Are eligible for Pulmonary Rehabilitation

Exclusion Criteria

  • • Unable to perform mild exercises
  • Patients with a high likelihood of being lost to follow-up or contact (patients with active chemical dependency), are planning to move out of the state, are not living in the healthcare area.
  • Patients with an inability to provide good data or follow commands (patients who are disoriented, have a severe neurologic or psychiatric condition).

Outcomes

Primary Outcomes

Quality of Life: Chronic Respiratory Questionaire

Time Frame: 8 weeks from the start of the intervention

To determine the effect of the proposed system on disease specific quality of life. The instrument has 2 summary scores, physical and emotional

Daily Physical Activity measured by Actigraph

Time Frame: 8 weeks from the start of the intervention

To determine the effectiveness of the proposed system, on daily physical activity measured by triaxial accelerometers

Study Sites (1)

Loading locations...

Similar Trials