Effects of Different Techniques of the Method Pilates in Chronic Low Back Pain
|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|
|Low Back Pain||Other: Pilates exercises with stabilization Other: Classic Pilates|
|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
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|