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
PHASE1
20 participants
INTERVENTIONAL
2010-02-28
2010-12-31
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
TREATMENT
NONE
Study Groups
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MBSR
Mindfulness Based Stress Reduction Program (MBSR)
Traditional eight-week MBSR Program.
Interventions
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Mindfulness Based Stress Reduction Program (MBSR)
Traditional eight-week MBSR Program.
Eligibility Criteria
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Inclusion Criteria
* clinically significant dyspnea, as determined by a score of \>=2 on the Medical Research Council of Dyspnea Score questionnaire (0-4).
Exclusion Criteria
* patients with an inability fo provide good data or to follow commands (neurologic or psychiatric condition).
* poor motivation or lack of interest in program
40 Years
99 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Roberto P. Benzo
M.D.
Principal Investigators
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Roberto Benzo, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Other Identifiers
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09-008478
Identifier Type: -
Identifier Source: org_study_id
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