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Comparison of Tai Chi and Pulmonary Rehabilitation on the Effect of Indacaterol in Treatment naïve COPD Participants

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Tai-chi plus Indacaterol
Pulmonary rehabilitation plus Indacaterol
Sponsored by
Yuan-Ming Luo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, Pulmonary rehabilitation

Eligibility Criteria

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

Inclusion Criteria:

  1. bronchodilator naïve patients
  2. Age 40-80 with GOLD II-IV COPD (post-bronchodilator FEV1 ≥ 25% and <80 % of the predicted normal, and a post-bronchodilator FEV1/FVC < 0.70)
  3. patients who are residents in Xingning city (Guangdong Province, China) will be recruited.

Exclusion Criteria:

  1. Patients currently or previous on any type of Tai Chi exercise or pulmonary rehabilitation
  2. Patients with a history of malignancy of any organ system treated or untreated, within the past 5 years.
  3. Patients with clinically significant renal, cardiovascular, neurological, metabolism, immunological, psychiatric, gastrointestinal, hepatic, or haematological abnormalities.
  4. Patients with concomitant pulmonary disease (e.g. asthma, lung fibrosis, primary bronchiectasis, sarcoidosis, interstitial lung disorder, tuberculosis)
  5. Patients with obesity (BMI> 40 kg/m2).
  6. Patients requiring long term oxygen therapy (> 12 h a day) on a daily basis for chronic hypoxemia or recovering from acute exacerbation less than 6 weeks.
  7. Patients with Asthma.

Sites / Locations

  • Xing-Ning Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Tai-Chi group

Pulmonary rehabilitation group

Arm Description

Tai-Chi exercise plus Indacaterol 150ug/day

Conventional exercise plus Indacaterol 150ug/day

Outcomes

Primary Outcome Measures

change in St. George's Respiratory Questionnaire (SGRQ)

Secondary Outcome Measures

Full Information

First Posted
October 28, 2015
Last Updated
October 12, 2016
Sponsor
Yuan-Ming Luo
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1. Study Identification

Unique Protocol Identification Number
NCT02665130
Brief Title
Comparison of Tai Chi and Pulmonary Rehabilitation on the Effect of Indacaterol in Treatment naïve COPD Participants
Official Title
State Key Laboratory of Respiratory Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Yuan-Ming Luo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Tai-Chi may be a beneficial form of rehabilitation which is acceptable to the Chinese population but no data exist concerning metabolic responses to Tai-Chi in COPD patients. Investigators conduct an Randomized controlled trial to evaluate the synergistic effect of a Long acting β2-agonists with Tai-Chi as a culturally acceptable form of PR in the Asian population. Classical western style pulmonary rehabilitation will serve as a comparator Investigators propose a prospective randomized controlled trial in which 120 bronchodilator naïve participants (Age 40-80 with GOLD II-IV COPD (post-bronchodilator FEV1 ≥ 25% and <80 % of the predicted normal, and a post-bronchodilator FEV1/FVC < 0.70) are randomized to receive a 26 weeks course of Indacaterol with either Tai-Chi or conventional Pulmonary Rehabilitation. Only participants who are residents in Xingning city (Guangdong Province, China) will be recruited. Both Tai-Chi and pulmonary rehabilitation will be given by qualified instructors at a rural location in southern China (Xingning). A qualified UK Physiotherapist will also be involved in the management of pulmonary rehabilitation program to further make sure the high quality of pulmonary rehabilitation has been applied. Both arm participants will also receive in an open label fashion Indacaterol 150µg qd. for 6 months giving 2 therapy groups (Tai-Chi/Indacaterol, pulmonary rehabilitation/Indacaterol). The primary endpoint of this study is change in SGRQ between Tai-Chi/Indacaterol and pulmonary rehabilitation/Indacaterol at 14 weeks after entry and the secondary endpoints are change in FEV1% and six minute walk distance. the planned recruitment will be 120 with a view to obtaining 100 completers. The investigators propose the study starts on 31 Dec 2014 and completes on 30 June, 2016.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD, Pulmonary rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tai-Chi group
Arm Type
Active Comparator
Arm Description
Tai-Chi exercise plus Indacaterol 150ug/day
Arm Title
Pulmonary rehabilitation group
Arm Type
Placebo Comparator
Arm Description
Conventional exercise plus Indacaterol 150ug/day
Intervention Type
Other
Intervention Name(s)
Tai-chi plus Indacaterol
Intervention Description
Participants perform Tai-chi exercise 5 days/week and take indacaterol 150ug/day for 24 weeks
Intervention Type
Other
Intervention Name(s)
Pulmonary rehabilitation plus Indacaterol
Intervention Description
Participants perform conventional exercise 5 days/week and take indacaterol 150ug/day for 24 weeks
Primary Outcome Measure Information:
Title
change in St. George's Respiratory Questionnaire (SGRQ)
Time Frame
14 weeks after intervention

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: bronchodilator naïve patients Age 40-80 with GOLD II-IV COPD (post-bronchodilator FEV1 ≥ 25% and <80 % of the predicted normal, and a post-bronchodilator FEV1/FVC < 0.70) patients who are residents in Xingning city (Guangdong Province, China) will be recruited. Exclusion Criteria: Patients currently or previous on any type of Tai Chi exercise or pulmonary rehabilitation Patients with a history of malignancy of any organ system treated or untreated, within the past 5 years. Patients with clinically significant renal, cardiovascular, neurological, metabolism, immunological, psychiatric, gastrointestinal, hepatic, or haematological abnormalities. Patients with concomitant pulmonary disease (e.g. asthma, lung fibrosis, primary bronchiectasis, sarcoidosis, interstitial lung disorder, tuberculosis) Patients with obesity (BMI> 40 kg/m2). Patients requiring long term oxygen therapy (> 12 h a day) on a daily basis for chronic hypoxemia or recovering from acute exacerbation less than 6 weeks. Patients with Asthma.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuan-Ming Luo, PhD
Organizational Affiliation
The Affiliated Hospital og Guangzhou Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xing-Ning Hospital
City
Meizhou
State/Province
Guangdong
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
29625777
Citation
Polkey MI, Qiu ZH, Zhou L, Zhu MD, Wu YX, Chen YY, Ye SP, He YS, Jiang M, He BT, Mehta B, Zhong NS, Luo YM. Tai Chi and Pulmonary Rehabilitation Compared for Treatment-Naive Patients With COPD: A Randomized Controlled Trial. Chest. 2018 May;153(5):1116-1124. doi: 10.1016/j.chest.2018.01.053. Epub 2018 Apr 3.
Results Reference
derived

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Comparison of Tai Chi and Pulmonary Rehabilitation on the Effect of Indacaterol in Treatment naïve COPD Participants

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