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Surface EMGdi Evaluate the Efficacy of Pulmonary Rehabilitation in Patients With COPD: a Multi Center Prospective Study

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD)

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Control group
Calibrated cycle ergometer
Threshold loading device
Calibrated cycle ergometer and threshold loading device
Sponsored by
Zhujiang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease (COPD) focused on measuring surface EMGdi, pulmonary rehabilitation, inspiratory muscle training, exercise training

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged over 40 years old.
  • Patients with pulmonary function test of forced expiratory volume at one second(FEV1)/forced vital capacity(FVC) < 70%.
  • Patients in a clinically stable state
  • Patients who signed informed consent.
  • No participation in other pulmonary rehabilitation program within the previous 2 months.

Exclusion Criteria:

  • Patients with signs of an airway infection.
  • Patients with metabolic disease and serious cardiovascular disease.
  • Patients with Multiple pulmonary bulla.
  • Patients with poor compliance.

Sites / Locations

  • Zhujiang Hospital,Southern Medical UniverstiyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Control group

Cycle training group

Inspiratory training group

Combined group

Arm Description

Neither cycle training nor inspiratory muscle training.

A calibrated cycle ergometer is used to do 30-minute cycling training session 3 days a week.

A threshold loading device is used to perform 21-minute inspiratory muscle training 3 days a week.

Calibrated cycle ergometer and threshold loading device are applied.A 30-minute cycle training is performed using calibrated cycle ergometer and a 21-minute inspiratory muscle training using threshold loading device 3 days a week.

Outcomes

Primary Outcome Measures

Diaphragmatic function(composite outcome measure)
Diaphragmatic function can be assessed by diaphragm electromyogram (EMGdi), which reflect the physiological activity of the diaphragm and indicate functional status of the central drive.

Secondary Outcome Measures

Inspiratory muscle function(composite outcome measure)
Currently, the maximal inspiratory pressure (PImax) and maximal expiratory pressures(PEmax) are measured by a digital manometer (AZ-8205, AZ Instrument, Taichung City, Taiwan)and combined to evaluate inspiratory muscle function.
Pulmonary Function(composite outcome measure)
Pulmonary function is measured using a spirometer(PonyFX 229, Cosmed, Rome, Italy) that is calibrated daily.The FEV1 and percent-of-predicted FEV1, FVC and percent-of-predicted FVC which are presented in one report are used to evaluate Pulmonary Function.
Cardiopulmonary exercise test(composite outcome measure)
Cardiopulmonary exercise test can help to reflect the variables,like maximaloxygen uptake(VO2max), anaerobic threshold (AT).
Degree of dyspnea(composite outcome measure)
Difference in the degree of dyspnea can be measured by Borg index.
Exercise capacity(composite outcome measure)
Exercise capacity is evaluated using the 6-min walking distance (6MWD) according to American Thoracic Society guidelines.

Full Information

First Posted
December 27, 2016
Last Updated
March 10, 2017
Sponsor
Zhujiang Hospital
Collaborators
Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangdong Pharmaceutical University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Nanfang Hospital, Southern Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03082924
Brief Title
Surface EMGdi Evaluate the Efficacy of Pulmonary Rehabilitation in Patients With COPD: a Multi Center Prospective Study
Official Title
Surface Diaphragm EMG Evaluate the Clinical Efficacy of Pulmonary Rehabilitation in Patients With Chronic Obstructive Pulmonary Disease: a Multi Center Prospective Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
July 2016 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
June 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhujiang Hospital
Collaborators
Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangdong Pharmaceutical University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Nanfang Hospital, Southern Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Pulmonary rehabilitation is recognized as a core component of the management of individuals with chronic obstructive respiratory disease, which has become first-line treatment besides drug therapy. However, in the current clinical evaluation system of pulmonary rehabilitation, there is still a lack of simple, objective index,which can be monitored at any time.Neural respiratory drive , as an important physiological index, is closely related to the symptoms and the severity of the disease. It may be a sensitive indicator to evaluate the effectiveness of pulmonary rehabilitation. Surface EMGdi can accurately evaluate neural respiratory drive , its detection is non-invasive, simple and safety . In recent years, with the development of signal detection and analysis technology, EMG recording is more stable, but as the related research samples were low, surface diaphragm EMG has not yet the establishment of standardization. Therefore, based on the previous work, the project was carried out in a multicenter randomized controlled study,in which the stable stage of COPD patients were included in different ways of pulmonary rehabilitation training, a comprehensive clinical assessment will be conducted before and after training. Compared with the traditional evaluation methods and standard esophageal diaphragmatic electromyography, surface EMGdi detect the changes of neural respiratory drive in patients with COPD,that can help to explore the application value of surface EMGdi in the assessment of chronic obstructive pulmonary disease with pulmonary rehabilitation, to provide a basis for the promotion of the diaphragm and the optimization of pulmonary rehabilitation program.
Detailed Description
The patients with COPD will participate in a rehabilitation program for 52 weeks. Participants in the proposed study will be randomly programmed into one of four intervention groups: Neither cycle training nor inspiratory muscle training. Cycle training program alone (performing on calibrated stationary cycle ergometer). Inspiratory muscle training alone (performing on threshold loading device). Combined cycle training and inspiratory muscle training(performing on calibrated stationary cycle ergometer and threshold loading device).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease (COPD)
Keywords
surface EMGdi, pulmonary rehabilitation, inspiratory muscle training, exercise training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Experimental
Arm Description
Neither cycle training nor inspiratory muscle training.
Arm Title
Cycle training group
Arm Type
Experimental
Arm Description
A calibrated cycle ergometer is used to do 30-minute cycling training session 3 days a week.
Arm Title
Inspiratory training group
Arm Type
Experimental
Arm Description
A threshold loading device is used to perform 21-minute inspiratory muscle training 3 days a week.
Arm Title
Combined group
Arm Type
Experimental
Arm Description
Calibrated cycle ergometer and threshold loading device are applied.A 30-minute cycle training is performed using calibrated cycle ergometer and a 21-minute inspiratory muscle training using threshold loading device 3 days a week.
Intervention Type
Device
Intervention Name(s)
Control group
Intervention Description
Neither cycle training nor inspiratory muscle training.
Intervention Type
Device
Intervention Name(s)
Calibrated cycle ergometer
Intervention Description
The most common device to perform cycle training is calibrated cycle ergometer.
Intervention Type
Device
Intervention Name(s)
Threshold loading device
Intervention Description
Threshold loading device is used to perform inspiratory muscle training.
Intervention Type
Device
Intervention Name(s)
Calibrated cycle ergometer and threshold loading device
Intervention Description
Combined cycle training and inspiratory muscle training.The threshold loading device is composed of a mouth -piece attached to a small plastic cylinder that contains a spring-loaded poppet value. The valve opens to permit inspiratory flow only once the person has generated adequate negative intrathoracic pressure to condense the spring.
Primary Outcome Measure Information:
Title
Diaphragmatic function(composite outcome measure)
Description
Diaphragmatic function can be assessed by diaphragm electromyogram (EMGdi), which reflect the physiological activity of the diaphragm and indicate functional status of the central drive.
Time Frame
Change from baseline in diaphragm electromyogram.(8 weeks later, 26 weeks later, 52 weeks later)
Secondary Outcome Measure Information:
Title
Inspiratory muscle function(composite outcome measure)
Description
Currently, the maximal inspiratory pressure (PImax) and maximal expiratory pressures(PEmax) are measured by a digital manometer (AZ-8205, AZ Instrument, Taichung City, Taiwan)and combined to evaluate inspiratory muscle function.
Time Frame
Change from baseline in inspiratory muscle function.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Pulmonary Function(composite outcome measure)
Description
Pulmonary function is measured using a spirometer(PonyFX 229, Cosmed, Rome, Italy) that is calibrated daily.The FEV1 and percent-of-predicted FEV1, FVC and percent-of-predicted FVC which are presented in one report are used to evaluate Pulmonary Function.
Time Frame
Change from baseline in pulmonary function.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Cardiopulmonary exercise test(composite outcome measure)
Description
Cardiopulmonary exercise test can help to reflect the variables,like maximaloxygen uptake(VO2max), anaerobic threshold (AT).
Time Frame
Change from baseline in cardiopulmonary exercise test.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Degree of dyspnea(composite outcome measure)
Description
Difference in the degree of dyspnea can be measured by Borg index.
Time Frame
Change from baseline in degree of dyspnea.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Exercise capacity(composite outcome measure)
Description
Exercise capacity is evaluated using the 6-min walking distance (6MWD) according to American Thoracic Society guidelines.
Time Frame
Change from baseline in exercise performance.(8 weeks later, 26 weeks later, 52 weeks later)
Other Pre-specified Outcome Measures:
Title
Body Composition Monitor(composite outcome measure)
Description
Body composition abnormalities are prevalent in COPD.Human body composition analyzer can detect various elements of human body and analyze human health status.
Time Frame
Change from baseline in body composition.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Health-related quality(composite outcome measure)
Description
Health-related quality is a component of the broader concept of quality of life and is defined as satisfaction with health.The St. George's Respiratory Questionnaire (SGRQ) and Chronic Respiratory Disease Questionnaire (CRQ);and its self-reported version are the most widely used disease-specific questionnaires.
Time Frame
Change from baseline in Health-related quality.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Symptom Evaluation(composite outcome measure)
Description
Individuals with chronic respiratory disease often have symptoms such as dyspnea, fatigue, cough, weakness,sleeplessness,and psychological distress.Instruments for assessment of multiple symptoms include COPD Assessment Test (CAT) and Modified Medical British Research Council Scale(mMRC).
Time Frame
Change from baseline in symptom evaluation.(8 weeks later, 26 weeks later, 52 weeks later)
Title
Depression and anxiety evaluation(composite outcome measure)
Description
Hospital Anxiety and Depression Scale (HADS) was found to perform well in assessing the symptom severity and caseness of anxiety disorders and depression in both somatic, psychiatric and primary care patients and in the general population.
Time Frame
Change from baseline in depression and anxiety evaluatione.(8 weeks later, 26 weeks later, 52 weeks later)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged over 40 years old. Patients with pulmonary function test of forced expiratory volume at one second(FEV1)/forced vital capacity(FVC) < 70%. Patients in a clinically stable state Patients who signed informed consent. No participation in other pulmonary rehabilitation program within the previous 2 months. Exclusion Criteria: Patients with signs of an airway infection. Patients with metabolic disease and serious cardiovascular disease. Patients with Multiple pulmonary bulla. Patients with poor compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liqing Wang, Doctor
Email
wliqing07@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xin Chen, Doctor
Email
chen_xin1020@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xin Chen, Doctor
Organizational Affiliation
Zhujiang Hospital,Southern Medical Unversity
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhujiang Hospital,Southern Medical Universtiy
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510282
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liqing Wang, Doctor
Email
wliqing07@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Surface EMGdi Evaluate the Efficacy of Pulmonary Rehabilitation in Patients With COPD: a Multi Center Prospective Study

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