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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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16 December 2017 |
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Main ID: |
NCT02468635 |
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Date of registration:
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30/05/2015 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Rehabilitation of Patients With Lung Chronic Obstructive Pulmonary Disease
PR |
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Scientific title:
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Analysis of Pulmonary Rehabilitation on the Physical Capacity and Pulmonary Function in Patients With Chronic Obstructive Pulmonary Disease Clinical Trial |
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Date of first enrolment:
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June 2015 |
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Target sample size:
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2 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02468635 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator).
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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Cássio Magalhães, research |
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Address:
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Telephone:
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+557199616304 |
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Email:
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cassiofisio2@yahoo.com.br |
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Affiliation:
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Name:
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Adelmir Machado, research |
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Address:
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Telephone:
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Email:
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Affiliation:
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Federal University of Bahia |
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Name:
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Cássio Magalhães, research |
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Address:
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Telephone:
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+557199616304 |
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Email:
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cassiofisio2@yahoo.com.br |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients with COPD eligible to moderate COPD according to the criteria of gold GOLD
(Global Initiative for Chronic Obstructive Lung Disease) and who had
post-bronchodilator spirometry results in the last year of FEV1 (forced expiratory
volume in one second) / FVC (forced vital capacity) <0.7 and FEV1 between 50% and 80%
of previsto.
- Besides being former smokers for at least three months and were clinically stable, no
disease exacerbation in the past three months.
- Accompanied by a pulmonologist.
- Age between 40-85 years.
- They are not practicing physical activity.
- Without cardiovascular or orthopedic disease that makes it impossible to perform the
exercises of the RP protocol.
- Without presenting other comorbidities that put them at risk during the exercises .
- Use of bronchodilators and oral theophylline, oxygen therapy or corticosteroids.
Exclusion Criteria:
- Patients who have musculoskeletal comorbidities that interfere with walking or
performing upper extremity exercises.
- lower peripheral saturation decrease of oxygen lower than 90% during the 6 minute walk
test (six) minutes.
- Presenting difficulty of cognitive understanding of body awareness and the ability to
recall information for the questionnaire responses applied in the evaluation and
re-evaluation in addition to this also children, adolescents and legally incapable
Age minimum:
40 Years
Age maximum:
85 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Chronic Obstructive Pulmonary Disease
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Intervention(s)
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Other: without training for upper limb
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Other: upper limb exercises
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Primary Outcome(s)
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Change in distance of the six-minute walk test
[Time Frame: 8 weeks]
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Secondary Outcome(s)
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Change in quality of life
[Time Frame: 8 weeks]
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Change in forced expiratory volume in one second
[Time Frame: 8 weeks]
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Change in forced vital capacity
[Time Frame: 8 weeks]
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repetition maximum (RM);
[Time Frame: 8 weeks]
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Change in respiratory muscle strength
[Time Frame: 8 weeks]
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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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