- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02189044
Pilates and Muscle Strength Respiratory
Effects of the Method Pilates Exercises in Muscle Strength Respiratory of Elderly Women: a Clinical Trial
Study Overview
Detailed Description
METHODOLOGY This study is a clinical, longitudinal, prospective trial conducted at the Laboratory of Kinesiology and Cinesioterapia of Physiotherapy, Federal University of Triangulo Mineiro - UFTM. All participants signed an informed consent. The research started after approval by the Ethics Committee UFTM Research Protocol (2147-2012).
Subject Initially the invitation was made to all students enrolled in the Open University of Third Age - UATI / UFTM from August to October 2012.
The selection was based on the following inclusion criteria: (1) age and above 60 years, (2) non-practicing regular physical activity, (3) availability to attend Pilates classes twice a week (in addition to the time UATI ) and (4) with preserved cognitive autonomy and exclusion criteria: history (1) diseases that directly affect the posture (disc herniation and angular deformities of the spine), (2) cardiovascular, respiratory and neurological diseases that prevent attainment of Pilates exercises, (3) impaired cognitive capacity limited autonomy or self-determination, (4) withdrawal of participation during the assessment process, and (5) two consecutive absences or a total of three absences during the proposed time for the training set.
Thus, the proposed methodology for this study was applied in seven women with a mean age of 64 ± 6 years.
Review / Procedures The assessment instruments were used: (1) Initial Assessment Sheet, (2) spirometer and (3) manometer.
The record initial assessment and spirometry were applied for the selection of participants. Through the initial evaluation form was possible to assess aspects of health status of participants (associated diseases, blood pressure, respiratory and heart rate, postural assessment) as well as information on personal history, family history and current medication .
A pulmonary function test (spirometry) was performed using the Vitalograph ® spirometer brand model 8600. Equipment was calibrated, and the tests were performed by a single trained and qualified examiner with instructions and standardized voice commands, as I standards advocated by Consensus Brazilian on Espirometria.12 Spirometry was performed to rule out any lung disease that affects the performance of the proposed exercises.
To assess respiratory muscle strength, the volunteers remained in the standing position using a nose clip. Respiratory muscle strength was obtained by the techniques of measurements of maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP), by means of an analog manometer Generate brand, scaled to ± 300 cmH2O, equipped with nozzle adapter, containing a hole 2 mm in diameter, serving as relief of muscles bocais.4 MIP valve was obtained with the maximal inspiration preceded by maximal expiration to residual volume level and MEP through the maximal expiration preceded by a maximal inspiration, to total lung capacity. Were performed at least three maneuvers maximal inspiratory pressure and maximal expiratory pressure, in order to obtain the greatest value from three acceptable.
The measurement of respiratory muscle strength occurred through an analog manometer (Ger-Air ®, São Paulo, Brazil), with scales - 300 to +300 cmH2O (calibrated), equipped with plastic trachea 16 cm long and 2.4 cm internal diameter, hard plastic mouthpiece and drain hole approximately 2 mm in diameter to dissipate the pressures generated by the muscles of the face and orofaringe.13 the maximal inspiratory pressure (MIP) and expiratory pressures were obtained maximum (MEP), carried a maximum of five times, acceptable and reproducible, and in the standing position, using a nose clip, for a time of sustained three seconds. The value of MIP was obtained from residual volume, and MEP from total lung capacity. Volunteers were due verbal encouragement and if there were more than 10% between a measure and another, a new difference maneuver was performed, considering the highest value since this was not the último.14 Therapeutic Intervention - Pilates Method The training through the Pilates exercises were performed in eleven weeks. The participants were instructed not to miss and attend classes twice a week. Each class consisted of five exercises lasting 40 minutes each lesson.
During the first four weeks (1 st to 4 th week) exercises performed were: Cat, Coffee Table, Single legcircle, pelvic movements, contraction of the glutes and closure was performed with posterior chain elongation range.
In the next four weeks (5th to 8th weeks) began a new series of exercises, which are: Bridge, Side Table, Bridge hip roll with legextension, Abdominal - halfhollup, obliques, and ultimately Stretching - Series of William's.
In the last four weeks of training (9th to 11th weeks) proposed a new series of exercises involving: Beaststroke, Support heel Bridge - hip roll with leg extension, and Hundred Squats with bat on the wall.
All exercises were performed during expiration. Statistical Analysis Descriptive data analysis was performed, with a mean and standard deviation. For comparative analysis of the data obtained in the pre-and post-intervention, the paired t test was applied (after confirmed the normal distribution of the sample - Shapiro Wilk test). The level of significance was set at 5%. The statistical program used was 18.0 SSPSS.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minas Gerais
-
Uberaba, Minas Gerais, Brazil, 38022200
- Lislei Jorge Patrizzi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age and above 60 years,
- non-practicing regular physical activity
- availability to attend Pilates classes twice a week (in addition to the time UATI)
- with preserved cognitive autonomy
Exclusion Criteria:
- history of diseases that directly affect the posture (disc herniation and angular deformities of the spine)
- cardiovascular, respiratory and neurological diseases that prevent attainment of Pilates exercises
- impaired cognitive autonomy or limited capacity for self-determination
- withdrawal of participation during the assessment process
- two consecutive absences or a total of three absences during the proposed training set for the time.
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: exercises; muscle strength
Evaluate the effects of Pilates exercises on respiratory muscle strength in elderly women before and after eleven weeks of training
|
The training through the Pilates exercises were performed in eleven weeks. Each class consisted of five exercises lasting 40 minutes each lesson. During the first four weeks exercises performed were: Cat, Coffee Table, Single legcircle, pelvic movements, contraction of the glutes and closure was performed with posterior chain elongation range. In the next four weeks began a new series of exercises, which are: Bridge, Side Table, Bridge hip roll with legextension, Abdominal - halfhollup, obliques, and ultimately Stretching - Series of William's. In the last four weeks of training proposed a new series of exercises involving: Beaststroke, Support heel Bridge - hip roll with leg extension, and Hundred Squats with bat on the wall. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Pulmonary function test (spirometry).
Time Frame: The results were obtained at the end of the eleven weeks of intervention
|
The results were obtained at the end of the eleven weeks of intervention
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Respiratory muscle strength
Time Frame: The results were obtained at the end of the eleven weeks of intervention
|
The results were obtained at the end of the eleven weeks of intervention
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lislei Patrizzi, Universidade Federal do triângulo Mineiro
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UFTM2014
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