CClinicalTrials.gg
CompletedNCT00373932Updated Dec 7, 2009

Real-Time Support for Exercise Persistence in COPD

A Phase 1/2 interventional study of Coached exercise persistence intervention and Self-Monitored exercise persistence intervention in Pulmonary Disease, Chronic Obstructive, COPD and Emphysema, sponsored by University of Washington. Completed at 1 site in United States. Open to participants aged 40 Years to 85 Years. Per ClinicalTrials.gov, last updated 2009-12-07.

Sponsored by University of Washington · Phase 1/2 and Interventional

Phase
Phase 1/2
Study type
Interventional
Enrollment
17
Allocation
Randomized
Ages
40 Years to 85 Years
Sex
All
01

Study 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).

Read the 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.

02

Conditions studied

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

Keywords

  • Exercise
  • Physical Activity
  • Adherence
03

In context

Bronchitis

268 studies on the registry are indexed under Bronchitis; 26 are open to participants now.

This study's enrollment of 17 is below the median of 120 across 184 interventional studies indexed under Bronchitis.

Browse Bronchitis studies →

Lead sponsor

University of Washington is the lead sponsor of 1,397 studies on the registry; 225 are open to participants now.

Of its 154 completed or terminated interventional studies of FDA-regulated products, 132 (86%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 85 Years
Sexes eligible
All
Accepts 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

Exclusion Criteria:

  • Illnesses such as bronchiectasis, active malignancies or other end stage diseases
  • Plans to continue in a maintenance program after rehabilitation.
05

Study design

Phase
Phase 1 / Phase 2
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
17 participants (actual)

Study arms

  • Experimental
    MOBILE-A

    Coached exercise persistence intervention

    Behavioral: Coached exercise persistence intervention

  • Active comparator
    MOBILE-B

    Self-monitored exercise persistence intervention

    Behavioral: Self-Monitored exercise persistence intervention

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

06

What researchers measure

Primary outcomes

  1. Exercise behavior

    Time frame: 3 & 6 Months

Secondary outcomes

  1. Self-efficacy for exercise

    Time frame: 3 & 6 Months

  2. Perception of support

    Time frame: 3 & 6 Months

  3. COPD exacerbation

    Time frame: 3 & 6 Months

  4. Exercise Performance

    Time frame: 3 & 6 months

  5. Health related quality of life

    Time frame: 3 & 6 months

07

Study locations

1 site
  • University of Washington
    Seattle, Washington 98195, United States
08

References and documents

Publications

  • Nguyen HQ, Steele BG, Dougherty CM, Burr RL. Physical activity patterns of patients with cardiopulmonary illnesses. Arch Phys Med Rehabil. 2012 Dec;93(12):2360-6. doi: 10.1016/j.apmr.2012.06.022. Epub 2012 Jul 5. PubMed 22772084 ↗
  • Nguyen HQ, Gill DP, Wolpin S, Steele BG, Benditt JO. Pilot study of a cell phone-based exercise persistence intervention post-rehabilitation for COPD. Int J Chron Obstruct Pulmon Dis. 2009;4:301-13. doi: 10.2147/copd.s6643. Epub 2009 Sep 1. PubMed 19750190 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 7, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00373932
Lead sponsor
University of Washington
Collaborators
National Institutes of Health (NIH)
First posted
Sep 8, 2006
Start date
May 2006
Primary completion
Dec 2008
Completion
Dec 2008
Last update
Dec 7, 2009

Study contacts

Huong Q. Nguyen, PhD
principal investigator · University of Washington

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2009. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion