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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT02329873 |
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Date of registration:
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15/12/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Respiratory Rehabilitation Exercises in Older Adults With Acute Exacerbations of Chronic Obstructive Pulmonary Disease
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Scientific title:
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Efficacy of the Respiratory Rehabilitation Exercise Training Package in Hospitalized Elderly Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease: Randomized Control Trial |
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Date of first enrolment:
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November 2011 |
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Target sample size:
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61 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02329873 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Contacts
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Name:
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Lin-Yu Liao, MS |
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Address:
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Telephone:
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Email:
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Affiliation:
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Chest Hospital, Ministry of Health and Welfare, Taiwan |
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Key inclusion & exclusion criteria
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Inclusion criteria:
1. diagnosed with moderate COPD with moderate acute exacerbation
2. over 65 years of age
3. conscious clear
4. with shortness of breath or dyspnea that was not caused by heart disease,
pneumothorax, or pulmonary edema
5. had received bronchodilator aerosol therapy or antibiotic treatment, but had not been
treated with an antitussive
Exclusion Criteria:
1. unstable vital signs
2. blood oxygen concentration lower than 90%
3. unstable psychological status, hemoptysis, pneumothorax, pulmonary edema, or using
the respirator
Age minimum:
65 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Chronic Obstructive Pulmonary Disease (COPD)
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Intervention(s)
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Behavioral: Respiratory rehabilitation exercise training
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Primary Outcome(s)
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Change from baseline in dyspnea at 4th day
[Time Frame: At baseline and at the 4th day of the study]
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Secondary Outcome(s)
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Change from baseline in sputum expectoration at 4th day
[Time Frame: At baseline and at the 4th day of the study]
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Change from baseline in exercise tolerance at 4th day
[Time Frame: At baseline and at the 4th day of the study]
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Change from baseline in cough severity at 4th day
[Time Frame: At baseline and at the 4th day of the study]
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Secondary ID(s)
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ER-100-202
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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