Respiratory Muscle Strength Clinical Trial
Official title:
Respiratory Muscle Strength and Function in Healthy Children
NCT number | NCT01436318 |
Other study ID # | HK 176-2011 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 2011 |
Est. completion date | September 2014 |
Verified date | September 2018 |
Source | University of Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Respiratory muscle strength training (RMST) is a potential treatment option that has been shown to increase strength and ventilatory function in critically ill patients, patients on ventilators and patients with mild neuromuscular weakness. Currently researchers are examining the role of inspiratory muscle strength training (IMST) in pressure performance of ventilator dependent children with Pompe disease. However, normal pressure-flow-timing responses of lung function are not well-characterized in healthy children. The purpose of this study is to measure RMST-induced changes in respiratory function in healthy children. Children will undergo one session of lung function and strength testing. By studying healthy children's respiratory function, this study will also help to develop more efficient respiratory muscle training exercise prescriptions for children with neuromuscular weakness and impaired respiratory function.
Status | Completed |
Enrollment | 7 |
Est. completion date | September 2014 |
Est. primary completion date | August 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 4 Years to 16 Years |
Eligibility |
Inclusion Criteria: - Male or female subjects 4-16 years of age. - Healthy subjects Exclusion Criteria: - Have primary pulmonary disease - Have primary neuromuscular disease - Have a connective tissue or autoimmune disease - Have had a respiratory infection with in 15 days prior to study date - Have acute aminoglycosides antibiotic therapy with in 15 days prior to study date - Have acute corticosteroids with in 15 days prior to study date - Have a need to use an inhaler routinely - Have hepatic failure - Have hematologic failure - Have participated in other studies related to medications or exercise - Have used tobacco products - Have other precautions |
Country | Name | City | State |
---|---|---|---|
United States | University of Florida | Gainesville | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Florida |
United States,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pulmonary Function Testing | Subjects will complete tidal flow-volume assessments and forced expiratory maneuvers. | Day 1 |
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