A Home-based Intervention to Promote Mindful Breathing Awareness Through Pursed-lip Breathing Training for COPD Patients
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03814980 |
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Recruitment Status :
Completed
First Posted : January 24, 2019
Last Update Posted : January 6, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| COPD Emphysema | Behavioral: mindful breathing application Device: application on a computer tablet | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 6 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Intervention Model Description: | Pilot study |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Home-based Intervention to Promote Mindful Breathing Awareness Through Pursed-lip Breathing Training for COPD Patients |
| Actual Study Start Date : | November 1, 2018 |
| Actual Primary Completion Date : | August 30, 2019 |
| Actual Study Completion Date : | August 30, 2019 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Pilot Study
Participants will be shown how to use a mindful breathing software application. The software will be used for 1 week. At the end of the week, participants will evaluate the software.
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Behavioral: mindful breathing application
Participants will use a mindful breathing application on a computer tablet. Device: application on a computer tablet a computer tablet |
- Test the feasibility of a mindful breathing application for COPD patients [ Time Frame: About 1 week ]Mindful Breathing Application on a computer tablet for COPD patients
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 40 Years to 99 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03814980
| United States, Minnesota | |
| Mayo Clinic in Rochester | |
| Rochester, Minnesota, United States, 55905 | |
| Principal Investigator: | Roberto P Benzo | Mayo Clinic |
| Responsible Party: | Roberto P. Benzo, M.D., Associate Professor of Medicine, Mayo Clinic |
| ClinicalTrials.gov Identifier: | NCT03814980 |
| Other Study ID Numbers: |
17-004445 |
| First Posted: | January 24, 2019 Key Record Dates |
| Last Update Posted: | January 6, 2020 |
| Last Verified: | January 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Respiratory Aspiration Emphysema Respiration Disorders Respiratory Tract Diseases Pathologic Processes |

