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The study was to evaluate the long term effects, over one year, of five airway clearance techniques used by people with cystic fibrosis (active cycle of breathing techniques, autogenic drainage, positive expiratory pressure and oscillating positive expiratory pressure (R-C Cornet and Flutter)). The primary outcome measure was forced expiratory volume in one second (FEV1)and the null hypothesis was that there are no differences among the regimens.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Other | Active cycle of breathing techniques |
|
| 2 | Other | Autogenic drainage |
|
| 3 | Other | R-C Cornet |
|
| 4 | Other | Flutter |
|
| 5 | Other | PEP |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Airway clearance technique | Procedure |
|
| Measure | Description | Time Frame |
|---|---|---|
| Forced expiratory volume in one second (FEV1) | 48 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Quality of life (Short Form-36 and Chronic Respiratory Questionnaire) | 48 weeks | |
| Exercise capacity (Modified shuttle test) | 48 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jennifer A Pryor, PhD | Royal Brompton & Harefield NHS Foundation Trust | Principal Investigator |
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| ID | Term |
|---|---|
| D003550 | Cystic Fibrosis |
| ID | Term |
|---|---|
| D010182 | Pancreatic Diseases |
| D004066 | Digestive System Diseases |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| D030342 |
| Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D007232 | Infant, Newborn, Diseases |