Effects of Different Techniques of the Method Pilates in Chronic Low Back Pain
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|ClinicalTrials.gov Identifier: NCT01533805|
Recruitment Status : Unknown
Verified February 2012 by Cintia Pereira de Souza, Universidade Gama Filho.
Recruitment status was: Not yet recruiting
First Posted : February 15, 2012
Last Update Posted : February 15, 2012
|Condition or disease||Intervention/treatment||Phase|
|Low Back Pain||Other: Pilates exercises with stabilization Other: Classic Pilates||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||Effects of Different Techniques of the Method Pilates in Chronic Low Back Pain in Women 46 to 60 Years|
|Study Start Date :||February 2012|
|Estimated Primary Completion Date :||September 2012|
|Estimated Study Completion Date :||December 2012|
Experimental: Pilates with stabilization
This group will do pilates exercises with a focus on control of segmental stabilization of the lumbar spine neutral.
Other: Pilates exercises with stabilization
This group will focus on exercises with core stabilizing muscles. The frequency will be 16 sessions lasting 1 hour.
Other Name: Pilates with stabilization segmental
Active Comparator: Classic Pilates
This group will make Pilates exercises its focus is on mobilization exercises of the lumbar spine.
Other: Classic Pilates
This group will make Pilates exercises its focus is on mobilization exercises of the lumbar spine. The frequency will be 16 sessions lasting 1 hour.
- Pain [ Time Frame: Up to 8 weeks ]low back pain will be assessed with numeric pain scale two times (pre and post-intervention)
- Endurance of the back extensor muscles [ Time Frame: Up to 8 weeks ]The endurance of the back extensor muscles will be assessed Biering-Sorensen test
- Activity of abdominis transversus [ Time Frame: Up to 8 weeks ]Will be assessed with Biofeedback pressure stabilizer
- Functional Limitation [ Time Frame: Up to 8 weeks ]Will be assessed Rolland Morris Test
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01533805
|Contact: Cintia P Souza, Bacheloremail@example.com|
|Contact: Elirez B Silva, Doctoralfirstname.lastname@example.org|
|Gama Filho University||Not yet recruiting|
|Rio de Janeiro, RJ, Brazil, 23050-260|
|Contact: Cintia P Souza, bachelor 2181320046 email@example.com|
|Principal Investigator:||Cintia P Souza, bachelor||University Gama Filho|