Diaphragm Activity During Incentive Spirometry and Diaphragmatic Breathing
- Conditions
- Diaphragm MobilityBreathing ExercisesIncentive SpirometryDiaphragmatic Breathing
- Interventions
- Device: DB, VI and FI
- Registration Number
- NCT00997737
- Lead Sponsor
- Hospital Sirio-Libanes
- Brief Summary
The objective of the present study is to evaluate diaphragm activity during three breathing exercises: diaphragmatic breathing (DB), flow-oriented (Triflo II)incentive spirometry and volume-oriented (Voldyne) incentive spirometry.
Seventeen healthy subjects will be studied (8 man and 9 woman).
- Detailed Description
Right diaphragmatic mobility will be evaluated by determining the craniocaudal displacement of the left branch of the portal vein using a B-mode ultrasound device (Logic 500, Pro Series®; General ElectricMedical Systems, Milwaukee, WI, USA). The ultrasound technician will use a 3.5 MHz convex transducer positioned in the right subcostal region, with the incidence angle perpendicular to the craniocaudal axis, in the direction of the inferior vena cava. Next, an intraparenchymal portal branch will be identified in the field of vision and its position will be traced with the curser during the forced inspiration and expiration. The craniocaudal displacement of these points will be considered to be the amount of right diaphragmatic mobility.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 17
- Being 18 to 40 years old
- Having a normal body mass index
- Being a non-smoker
- Not knowing the DB and the IS techniques
- Reporting the absence of respiratory diseases.
- Presenting alteration in respiratory function detected by functional analysis of lung volume and capacity
- Inability to understand or perform the procedure.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description DB, VI and FV DB, VI and FI Breathing exercises
- Primary Outcome Measures
Name Time Method ultrasound evaluation of the diaphragm mobility six - eight months
- Secondary Outcome Measures
Name Time Method pulmonary function test six - eight months
Trial Locations
- Locations (1)
Instituto de Ensino e Pesquisa do Hospital Sírio Libanês
🇧🇷São Paulo, SP, Brazil