Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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COMPLETED
NA
65 participants
INTERVENTIONAL
2015-07-21
2018-10-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Pulmonary Rehabilitation
One arm study - all participants will go to pulmonary rehabilitation, received questionnaires, Dual-energy X-ray absorptiometry (DEXA) scans, Dynamometer and gait speed tests and activity measured through an activity monitor.
Pulmonary Rehabilitation
Measures of frailty taken before and after pulmonary rehabilitation.
Dynamometer
Grip Test
DEXA
Body Composition Testing
Gait Speed Test
15 foot walk test
Activity Monitor
Measures energy expenditure and activity
Questionnaires
Health-related questionnaires measuring self-reported exhaustion, emotions and disease symptoms.
Interventions
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Pulmonary Rehabilitation
Measures of frailty taken before and after pulmonary rehabilitation.
Dynamometer
Grip Test
DEXA
Body Composition Testing
Gait Speed Test
15 foot walk test
Activity Monitor
Measures energy expenditure and activity
Questionnaires
Health-related questionnaires measuring self-reported exhaustion, emotions and disease symptoms.
Eligibility Criteria
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Inclusion Criteria
* consenting to research
Exclusion Criteria
18 Years
ALL
No
Sponsors
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National Heart, Lung, and Blood Institute (NHLBI)
NIH
Mayo Clinic
OTHER
Responsible Party
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Cassie C. Kennedy, M.D.
Consultant for Critical Care Medicine
Principal Investigators
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Cassie Kennedy, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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15-001230
Identifier Type: -
Identifier Source: org_study_id
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