The effect of water-based exercise in chronic obstructive pulmonary disease
- Conditions
- Chronic obstructive pulmonary diseaseRespiratory - Chronic obstructive pulmonary disease
- Registration Number
- ACTRN12606000408583
- Lead Sponsor
- Prince of Wales Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 45
Confirmed diagnosis of chronic obstructive pulmonary disease; stable condition; presence of one or more co-morbid conditions (BMI> or equal to 32, musculoskeletal conditions affecting the lumbar spine or lower limbs, neurolocical conditions, neuromuscular disorders and one or more lower-limb joint replacements restricting mobility and/or joint range of motion). Both male and female subjects will be included with no age limits as long as the inclusion crieria are met.
Unstable cardiac disease, contra-indications to aquatic therapy, completed a pulmonary rehabilitation program in the last 12 months or attending maintenance exercise, inability to understand English, cognitive decline.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional exercise capacity measured by six-minute walk test, incremental shuttle walk test, endurance shuttle walk test. [At baseline and at 8 weeks.];Quality of life measured by St George Respiratory Questionnaire, SF-36 and Chronic Respiratory Disease Questionnaire.[At baseline and at 8 weeks.]
- Secondary Outcome Measures
Name Time Method Hospital Anxiety and Depression Scale[Measured at initial assessment and at completion of the 8 weeks intervention or usual care.];Lung function[Measured at initial assessment and at completion of the 8 weeks intervention or usual care.];respiratory muscle strength.[Measured at initial assessment and at completion of the 8 weeks intervention or usual care.];Acceptability of water-based training[At the completion of the 8 weeks intervention];Compliance[At the completion of the 8 weeks intervention]