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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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12 December 2020 |
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Main ID: |
NCT02550821 |
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Date of registration:
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13/09/2015 |
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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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Comparison of Physical Activity Level Between Patients With Bronchiectasis and Healthy Subjects
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Scientific title:
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Comparison of Physical Activity Level Between Patients With Bronchiectasis and Healthy Subjects |
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Date of first enrolment:
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September 2015 |
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Target sample size:
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76 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02550821 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Turkey
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Contacts
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Name:
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ASLIHAN CAKMAK |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hacettepe University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
Inclusion criteria of the Bronchiectasis Group:
1. Diagnosis of bronchiectasis
2. Being 18 years of age or older
3. Able and willing to complete the informed consent process.
4. Able to walk and co-operate
Exclusion Criteria:
Exclusion criteria of Bronchiectasis Group:
1. Unstable medical condition
2. To have severe neurological, orthopedic problems or severe heart failure.
The control group will consist of healthy subjects.
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Bronchiectasis
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Primary Outcome(s)
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Number of steps on accelerometer
[Time Frame: Seven days]
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Energy expenditure on activity monitor
[Time Frame: Seven days]
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Exercise capacity using 6-minute walk test and incremental shuttle walk test
[Time Frame: 8th day (after using device)]
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Physical activity level using International Physical Activity Questionnaire
[Time Frame: 8th day]
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Secondary Outcome(s)
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Quality of Life using St. George Respiratory Questionnaire
[Time Frame: 1st day]
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Peripheral muscle strength test using a hand-held dynamometer
[Time Frame: 8th day (after using device)]
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Shortness of breath using the Modified Medical Research Council Dyspnea Scale
[Time Frame: 1st day (before using device)]
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Maximal inspiratory and expiratory pressures measurement using a mouthpiece device
[Time Frame: 8th day (after using device)]
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Secondary ID(s)
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GO 15/313
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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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