Mindfulness Based Stress Reduction in COPD

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:

Mindfulness Based Stress Reduction in COPD

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01058499
• Other study ID #: 09-008478
• Status: Completed
• Phase: Phase 1
• First received: January 27, 2010
• Last updated: April 18, 2012
• Start date: February 2010
• Est. completion date: December 2010

Study information

• Verified date: April 2012
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to test the efficacy of a Mindfulness Based Stress Reduction program in COPD on quality of life, dyspnea, daily physical activity and mindfulness during daily life.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: December 2010
• Est. primary completion date: September 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 40 Years and older

Eligibility

Inclusion criteria:

• clinical diagnosis of COPD

• 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 a high likelihood of not completing the program (active chemical dependency)

• patients with an inability fo provide good data or to follow commands (neurologic or psychiatric condition).

• poor motivation or lack of interest in program

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Obstructive Pulmonary Disease
• COPD
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Behavioral:
• Mindfulness Based Stress Reduction Program (MBSR)
Traditional eight-week MBSR Program.

Locations

Country	Name	City	State
United States	Mayo Clinic in Rochester	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	We hypothesize that the perception of well being will increase after participants go through the MBSR program for COPD.		Baseline and at eight weeks	No
Secondary	Participants in the MBSR for COPD will have an increase in their physical activity level.		Baseline and 8 weeks	No