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Real-Time Support for Exercise Persistence in COPD

Real-Time Support for Exercise Persistence in COPD

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00373932
Enrollment
17
Registered
2006-09-08
Start date
2006-05-31
Completion date
2008-12-31
Last updated
2009-12-07

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

Conditions

Chronic Bronchitis, COPD, Emphysema, Pulmonary Disease, Chronic Obstructive

Keywords

Exercise, Physical Activity, Adherence

Brief summary

The purpose of this exploratory study is to determine the feasibility, acceptability, and efficacy of an exercise persistence intervention for patients with chronic obstructive pulmonary disease (COPD) following pulmonary rehabilitation (PR).

Detailed description

Exercise, a cornerstone of PR, is effective in improving dyspnea, functioning, and health related quality of life (HRQL) in patients with COPD. However, these improvements gradually dissipate following program completion. There are currently few successful interventions that support patients' persistence with community-based exercise after PR and that have closely monitored the potentially negative impact that COPD exacerbations have on exercise behaviors. Emerging technologies such as wirelessly enabled personal digital assistants (PDA) may provide an innovative means to support exercise persistence through real-time collaborative monitoring of exercise and signs and symptoms of COPD exacerbations and reinforcement to enhance exercise self-efficacy. Patient graduates of two PR programs who have COPD (n=20) will first undergo a 2-week run-in prior to being randomized to either the MOBILE (Mobilizing Support for Long-term Exercise) intervention or attention control for 6 months.

Interventions

BEHAVIORALCoached exercise persistence intervention

Collaborative symptom and exercise monitoring and weekly reinforcement for exercise persistence from nurse coach via a mobile device and telephone.

BEHAVIORALSelf-Monitored exercise persistence intervention

Self-monitoring of symptoms and exercise using a mobile device

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Moderate to severe COPD (FEV1/FVC \<70% and FEV1%\<80%) * Ability to speak, read and write English * Age 40 or older * Willingness to complete a 6 month program

Exclusion criteria

* Illnesses such as bronchiectasis, active malignancies or other end stage diseases * Plans to continue in a maintenance program after rehabilitation.

Design outcomes

Primary

MeasureTime frame
Exercise behavior3 & 6 Months

Secondary

MeasureTime frame
Self-efficacy for exercise3 & 6 Months
Perception of support3 & 6 Months
COPD exacerbation3 & 6 Months
Exercise Performance3 & 6 months
Health related quality of life3 & 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026