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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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13 March 2023 |
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Main ID: |
NCT03420209 |
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Date of registration:
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27/01/2018 |
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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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The Effect of Proprioceptive Neuromuscular Facilitation (PNF) Technique for Children With Chronic Pulmonary Diseases.
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Scientific title:
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The Effect of Proprioceptive Neuromuscular Facilitation Technique on Respiratory Functions, Functional Capacity, Muscle Force, Posture, Activity of Daily Living, Quality of Life for Children With Chronic Pulmonary Diseases. |
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Date of first enrolment:
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December 1, 2016 |
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Target sample size:
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40 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03420209 |
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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: Single (Participant).
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Phase:
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N/A
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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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Zerrin Dr Yigit, Prof |
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Address:
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Telephone:
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Email:
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Affiliation:
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Istanbul University, Cardiology Institute, Cardiology Department |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Patients between the ages of 10-18 years
2. Walking alone
3. The children with chronic pulmonary diseases who can cooperate
4. Children who can accommodate to the programme
5. The family who gave informed consent
6. The children who are didn't at the acute exacerbation attack.
Exclusion Criteria:
1. The children can't walk alone
2. The children with chronic pulmonary diseases who can't cooperate
3. The family who didn't gave informed consent
4. The children who are at the acute exacerbation attack.
Age minimum:
10 Years
Age maximum:
18 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Cystic Fibrosis
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Bronchiectasis
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Chronic Respiratory Disease
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Intervention(s)
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Behavioral: Group applying PNF technique
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Primary Outcome(s)
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Pulmonary function test
[Time Frame: 12 weeks]
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Secondary Outcome(s)
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Maximal inspiratory pressure and Maximal expiratory pressure measurement
[Time Frame: 12 weeks]
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6 Minutes Walk Test
[Time Frame: 12 weeks]
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Posture Analysis
[Time Frame: 12 weeks]
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Glitter-Activity of Daily Living test, Activity of Daily living measurement
[Time Frame: 12 weeks]
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The Pediatric Quality of Life Inventory (PedsQ-L)test
[Time Frame: 12 weeks]
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Muscle testing
[Time Frame: 12 weeks]
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6 Minutes Pegboard and Ring Test
[Time Frame: 12 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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