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NCT01905982 Clinical Trial

The Effect of Reflective Breathing Therapy Compared With Conventional Breathing Therapy in Patients With Chronic Obstructive Pulmonary Disease (COPD) III-IV; part2

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:
The Effect of Reflective Breathing Therapy Compared With Conventional Breathing Therapy on Dyspnoea, Activity and Parasympathetic Activities in Patients With COPD III-IV

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01905982
Other study ID # RAT 2013
Secondary ID KBerchtesgadener
Status Recruiting
Phase N/A
First received
Last updated
Start date January 2016
Est. completion date March 2020

Study information
Verified date June 2019
Source Klinikum Berchtesgadener Land der Schön-Kliniken
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether different types of breathing therapies in patients with COPD III-IV decrease dyspnea, increase activity and have impact on parasympathetic activities.

Recruitment information / eligibility
Status Recruiting
Enrollment 44
Est. completion date March 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- inpatient rehabilitation

- COPD (Gold stage III and IV)

Exclusion Criteria:

- severe exacerbation in the last four weeks

- acute infections

- fever

- neuritides

- severe osteoporosis

- skin disease

- manic depression

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• reflectory breathing therapy
duration:2x60 minutes
• conventional breathing therapy
duration:4x30 minutes

Locations
Country Name City State
Germany Schön Klinik Berchtesgadener Land Schönau Bayern

Sponsors (1)
Lead Sponsor Collaborator
Klinikum Berchtesgadener Land der Schön-Kliniken

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in BORG-Scale Instrument for self-reported dyspnea; modified BORG-scale ranges from 1 (no dyspnea) to 10 (maximum dyspnea) Change from pre (minute 0) in Borg Scale and directly post intervention
Secondary Change in lung volume measured by a bodyplethysmograph change from pre (minute0) in residual volume to post intervention
Secondary physical activity measured by Senswear 48 h post intervention
Secondary parasympathetic activities measured via Biofeedback baseline and post intervention
Secondary Chronic Respiratory Questionnaire health related quality of life baseline and post intervention
Secondary COPD Assessment Test health related Quality of life baseline and post intervention
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