A Home-based Module to Promote Mindful Breathing Awareness for COPD Patients

Sponsor
Mayo Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT04517500
Collaborator
National Center for Complementary and Integrative Health (NCCIH) (NIH)
60
1
2
18.8
3.2

Study Details

Study Description

Brief Summary

The purpose of this study is to develop a mindful breathing module to an already effective and developed home based rehabilitation program for guiding COPD patients in a mindful breathing practice and further palliate breathlessness and anxiety.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Home-based pulmonary rehabilitation program
  • Behavioral: Mindful breathing module
  • Behavioral: Health coaching
N/A

Detailed Description

A breathing technique called Pursed Lipped Breathing (PLB) has been proven to be beneficial for patients with COPD. PLB can ease shortness of breath and reduce stress and anxiety. This study will develop a mindful PLB module to compliment an already developed home based pulmonary rehabilitation program. In this study, patients will be randomized to either a group that does the home based pulmonary rehabilitation with the mindful breathing module and health coaching or a group that does the home based pulmonary rehabilitation with health coaching without the mindful breathing module. Both groups will do the home based pulmonary rehabilitation for 12 weeks. In addition there are questionnaires and the wearing of an activity monitor when you sign up and at 3 and 6 months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
A Home-based Intervention to Promote Mindful Breathing Awareness Through Pursed-lip Breathing Training for COPD Patients
Actual Study Start Date :
Aug 6, 2021
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Feb 28, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Home-base pulmonary rehabilitation with mindful breathing modu

Subjects will complete in a home-based pulmonary rehabilitation program and in addition will complete a mindful breathing practice using a module on a computer tablet.

Behavioral: Home-based pulmonary rehabilitation program
Subjects will wear an activity monitor while doing at home exercises using a computer tablet

Behavioral: Mindful breathing module
Additional module on the computer tablet that involves inhaling and exhaling while following an animated ball on the computer screen.

Behavioral: Health coaching
Weekly coaching calls to discuss rehabilitation and health process using motivational interviewing

Active Comparator: Home-base pulmonary rehabilitation

Subjects will complete 12 week home-based pulmonary rehabilitation with health coaching

Behavioral: Home-based pulmonary rehabilitation program
Subjects will wear an activity monitor while doing at home exercises using a computer tablet

Behavioral: Health coaching
Weekly coaching calls to discuss rehabilitation and health process using motivational interviewing

Outcome Measures

Primary Outcome Measures

  1. Change in Chronic Respiratory Disease Questionnaire (CRQ)- Dyspnea Summary [The change from baseline of the CRQ will be assessed at 3 and 6 month.]

    The CRQ is a 20-question inventory assessing the areas of health related quality of life in dyspnea (shortness of breath), fatigue, emotion, and feelings of mastery of chronic respiratory disease. The Dyspnea Summary score includes dyspnea (symptom #1 in COPD) and fatigue (symptom #2 in COPD) domains. The questions in each domain are added together and then divided by the number of questions. The possible range is 1-7, where 1 is the worst and 7 the best.

  2. Change in Chronic Respiratory Disease Questionnaire (CRQ)- Emotions Summary [The change from baseline of the CRQ will be assessed at 3 and 6 month.]

    The CRQ Emotion Summary score includes the emotion (independent factor for admissions and poor quality of life) and mastery (self-management) domains of the CRQ. The scores for each domain are calculated by simply added together the answers and then dividing by the number of questions, the range is 1-7 where 1 is the worst and 7 the best.

Secondary Outcome Measures

  1. Change in daily Physical Activity- daily steps [The change from baseline on daily Physical activity will be assessed at 3 and 6 month.]

    An Actigraph activity monitor will be used to measure daily steps and activity counts. The activity monitor is wrist worn for 7 days.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults, age ≥ 40 years old.

  • Clinical diagnosis of Chronic Obstructive Pulmonary Disease (COPD).

  • At least 10 pack years of smoking.

Exclusion Criteria:
  • Unable to do mild exercise (orthopedic-neurologic problems or confined to a bed).

  • Unable to follow commands (cognitive impairment).

  • Have a high likelihood of being lost to follow-up (active alcohol or drug abuse).

  • Live in an area that does not have cellular service (Verizon).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Rochester Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic
  • National Center for Complementary and Integrative Health (NCCIH)

Investigators

  • Principal Investigator: Roberto P Benzo, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Roberto P. Benzo, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT04517500
Other Study ID Numbers:
  • 19-012772
  • 2R44AT009665-02
First Posted:
Aug 18, 2020
Last Update Posted:
Sep 29, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 29, 2021