Efficacy of Osteopathic Manipulation in Chronic Obstructive Pulmonary Disease
NCT ID: NCT00034112
Last Updated: 2006-08-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
INTERVENTIONAL
2001-04-30
2002-03-31
Brief Summary
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Detailed Description
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Participants in this study will be randomly assigned to receive either OMT or sham treatments once a week for 13 weeks. Outcome measures will be obtained at baseline; immediately following the first treatment; at 4, 8, and 12 weeks after initiation of treatment; and 4 weeks after termination of the treatment. Outcome variables include pulmonary function tests; quality-of-life questionnaires (including emotional functioning, fatigue, and dyspnea); and measurements of exercise tolerance and chest wall mobility.
Conditions
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Keywords
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Study Design
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RANDOMIZED
TREATMENT
Interventions
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osteopathic manipulative treatment
Eligibility Criteria
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No
Sponsors
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National Center for Complementary and Integrative Health (NCCIH)
NIH
Principal Investigators
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Donald R. Noll
Role: PRINCIPAL_INVESTIGATOR
Kirksville College of Osteopathic Medicine
Locations
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Kirksville College of Osteopathic Medicine
Kirksville, Missouri, United States
Countries
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Other Identifiers
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