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Home-based Health Management of Chronic Obstructive Lung Disease (COPD) Patients

Home-based Health Management of COPD Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02999685
Enrollment
154
Registered
2016-12-21
Start date
2016-09-30
Completion date
2019-06-30
Last updated
2020-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease, Emphysema, Pulmonary Rehabilitation

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.

Interventions

BEHAVIORALHome-base Pulmonary Rehab with Health Coaching

Sponsors

Minnesota HealthSolutions
CollaboratorINDUSTRY
Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 99 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life: Chronic Respiratory Questionaire8 weeks from the start of the interventionTo 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 Actigraph8 weeks from the start of the interventionTo determine the effectiveness of the proposed system, on daily physical activity measured by triaxial accelerometers

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026