Use of Internet Mediated Walking Program and Pedometer in COPD
This study is currently recruiting participants.
Verified January 2013 by VA Boston Healthcare System
Sponsor:
VA Boston Healthcare System
Collaborator:
University of Michigan
Information provided by (Responsible Party):
Marilyn Moy, VA Boston Healthcare System
ClinicalTrials.gov Identifier:
NCT01772082
First received: January 16, 2013
Last updated: January 18, 2013
Last verified: January 2013
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Purpose
Persons with COPD are randomized to pedometer versus pedometer plus Internet mediated website to promote walking and physical activity. Primary outcome is 6-minute walk test distance. Intervention lasts 3 months.
| Condition | Intervention |
|---|---|
|
COPD |
Behavioral: Internet mediated walking program |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Randomized Study of Use of Internet Mediated Walking Program and Pedometer in COPD |
Further study details as provided by VA Boston Healthcare System:
Primary Outcome Measures:
- 6-minute walk test distance [ Time Frame: pre and 3 months post ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 130 |
| Study Start Date: | January 2012 |
| Estimated Primary Completion Date: | June 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Pedometer alone
pedometer
|
Behavioral: Internet mediated walking program
none
|
|
Experimental: Pedometer plus website
pedometer and website
|
Behavioral: Internet mediated walking program
none
|
Eligibility| Ages Eligible for Study: | 40 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
COPD, ability to walk, has Internet access
Exclusion Criteria:
COPD exacerbation in previous 4 weeks
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01772082
Locations
| United States, Massachusetts | |
| VABoston Healthcare System | Recruiting |
| Boston, Massachusetts, United States, 02132 | |
| Contact: Marilyn Moy, MD 857-203-6622 marilyn.moy@va.gov | |
| Principal Investigator: Marilyn Moy, MD | |
Sponsors and Collaborators
VA Boston Healthcare System
University of Michigan
More Information
No publications provided
| Responsible Party: | Marilyn Moy, Assistant Professor of Medicine, VA Boston Healthcare System |
| ClinicalTrials.gov Identifier: | NCT01772082 History of Changes |
| Other Study ID Numbers: | ESCFull2328 |
| Study First Received: | January 16, 2013 |
| Last Updated: | January 18, 2013 |
| Health Authority: | United States: Federal Government, VA Rehab R&D |
Additional relevant MeSH terms:
|
Pulmonary Disease, Chronic Obstructive Lung Diseases, Obstructive Lung Diseases Respiratory Tract Diseases |
ClinicalTrials.gov processed this record on May 16, 2013