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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01449643
Other study ID # CAAE-0280.0.172.000-10
Secondary ID
Status Completed
Phase N/A
First received October 6, 2011
Last updated October 28, 2011
Start date September 2010
Est. completion date August 2011

Study information

Verified date October 2011
Source Universidade Federal de Pernambuco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is whether an inspiratory muscle training protocol would be associated with an improvement in of the diaphragm mobility, an increase in pulmonary function values , gain strength and endurance of respiratory muscles and improving quality of life.


Description:

Few studies have investigated the effects of an inspiratory muscle training in obese patients on the diaphragmatic mobility and thickness. Obesity, especially morbid, triggers changes in the respiratory system, which can affect the work activities and daily life of individuals with this multifactorial syndrome. These functional changes in mechanical ventilation may be linked to weakness and poor respiratory muscle strength, so by promoting rehabilitation of these muscles can minimize the losses that come with obesity


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- BMI > 40 kg/m²

- Absence of acute or chronic lung disease

Exclusion Criteria:

- Acute or chronic inflammatory process

- Thyroid disorders

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Threshold

Sham Threshold


Locations

Country Name City State
Brazil Universidade Federal de Pernambuco Recife Pernambuco

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal de Pernambuco

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ultrasound evaluation of the diaphragm mobility Compare and correlate diapgragm excursion with pulmonary function. 3 months
Secondary Pulmonary function test 3 months
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