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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04929990
Other study ID # CF18259A
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 7, 2018
Est. completion date June 2, 2021

Study information

Verified date June 2021
Source Taichung Veterans General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with COPD and MCI received either inspiratory muscle training or inspiratory plus expiratory muscle training and compared the therapeutic effects


Description:

Patients with COPD and MCI were recruited, and were randomly assigned to the experimental group and the control group. The experimental group consisted of EMT and IMT for a total of 8 weeks, while the control group received IMT only. Outcomes measured and compared in this cohort were diaphragmatic thickness fraction and excursion examined by ultrasound, the dyspnea score of modified Medical Research Council (mMRC), the cognitive score of Mini-Mental State Examination (MMSE), and the score of COPD Assessment Test (CAT). In addition, the pulmonary function test, the cardiopulmonary exercise test, and the physiology performance of six minute walking test were also obtained. We also analyzed the difference of each parameters before and after training in each patient.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date June 2, 2021
Est. primary completion date April 6, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - 1. Having definite diagnosis of COPD, namely the value of the FEV1 divided by forced vital capacity (FVC) 10 to 15 minutes after beta-2 agonist inhalation being less than 0.7. - 2. The score of Mini-Mental State Examination (MMSE) being between 23 and 27 Exclusion Criteria: - 1. Being not able to follow instructions on respiratory muscle training or complete the questionnaires of our study due to cognitive impairment. - 2. Having difficulty to complete the cardiopulmonary exercise testing or the six minute walking test (6MWT) due to high risk cardiopulmonary diseases or other orthopedic conditions. - 3. Having the diagnosis of lung cancer or history of receiving thoracoabdominal surgery - 4. Having Body Mass Index more than 30

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Respiratory muscle training
Inspiratory and expiratory muscle training were performed using a breathing trainer (Dofin DT11/14, Galemed Co. Ltd, Taiwan) for 30 minutes a day with a total of eight weeks. Before the training, the MIP and maximal expiratory pressure (MEP) were documented by the best performance of three trials with a digital pressure gauge (GB60, Jitto International Co. Ltd, Taiwan)

Locations

Country Name City State
Taiwan Taichung Veterans General Hospital Taichung

Sponsors (1)

Lead Sponsor Collaborator
Taichung Veterans General Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary MMSE Mini-Mental State Examination 8 weeks
Secondary Diaphragmatic thickness fraction Diaphragmatic thickness fraction on ultrasonography 8 weeks
Secondary chronic obstructive pulmonary disease assessment test (CAT) questionnaire of dyspnea 8 weeks
Secondary diffusing capacity of the lung for carbon monoxide (DLCO) diffusing capacity of the lung for carbon monoxide (DLCO) in pulmonary function test 8 weeks
Secondary dead space fraction (Vd/Vt) dead space fraction (Vd/Vt) in cardiopulmonary function test 8 weeks
Secondary the distance walked in 6 minutes the distance walked in 6 minutes 8 weeks
Secondary Diaphragmatic excursion Diaphragmatic excursion on ultrasonography 8 weeks
Secondary forced vital capacity forced vital capacity tested in pulmonary function test 8 weeks
Secondary forced expiratory volume in 1 second forced expiratory volume in 1 second in pulmonary function test 8 weeks
Secondary forced expiratory volume in 1 second divided by forced vital capacity forced expiratory volume in 1 second divided by forced vital capacity in pulmonary function test 8 weeks
Secondary DLCO divided by alveolar volume (VA) DLCO divided by alveolar volume (VA) in pulmonary function test 8 weeks
Secondary modified Medical Research Council (mMRC) questionnaire of dyspnea 8 weeks
Secondary minute ventilation to carbon dioxide output (VE/VCO2) slope minute ventilation to carbon dioxide output (VE/VCO2) slope in cardiopulmonary function test 8 weeks
Secondary the change of oxygen saturation in 6 minutes walking test the change of oxygen saturation in 6 minutes walking test 8 weeks
Secondary the change of Borg scale in 6 minutes walking test the change of Borg scale in 6 minutes walking test 8 weeks
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