- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03377959
Effects of Pilates Method in the Range of Ballerina's Turnout (PilatesTurnout)
April 24, 2019 updated by: Aline Nogueira Haas, Federal University of Rio Grande do Sul
Effects of Pilates Method in the Range of Young Ballerina's Turnout
A high degree of turnout is desired by many dancers, because enables an efficient weight transfer; provides an excellent extension and control; and reduces the risk of injury when used properly.
The dancer's body conditioning is worked and acquired through various types of training, among which stands out the Pilates Method.
Thus, the aim of the study is to determine the effect of a training program of Pilates Method in the range of ballerinas' turnout.
The study will be conducted with young dancers, between 10 and 14 years, who practice classical dance twice a week.
They will be randomly divided into two groups: intervention and control, but only the intervention group will do Pilates classes.
To verify the extent of the turnout, tests will be applied in both groups, before the start of Pilates classes (pre-test) and after 24 sessions (post-test).
In the evaluation protocol will be collected kinematic data, while performing the movements of demi plié and elevé.
Anthropometric variables of height and body mass will be obtained; and also the extent of the passive and active turnout in dancers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
22
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rio Grande Do Sul
-
Porto Alegre, Rio Grande Do Sul, Brazil, 90690-200
- Laboratório de Pesquisa do Exercício
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 14 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- be female; age between 10 and 14 years; have practiced classical ballet classes for at least three years; attend classical ballet classes at least twice a week; have a minimum frequency of 80% during the whole intervention period.
Exclusion Criteria:
- present some injury during intervention period and data collection; have more than two consecutive absences in classical ballet and Pilates classes; not to continue with their routine of physical activities throughout the intervention period.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Pilates Group
Pilates Method Mat classes and Ballet Classes three times a week, totaling 24 session of each.
|
The intervention, the exercises, and their progressions were systematized based on protocol proposed by Siler (2008).
The intervention is ballet classes three times a week, 1 hour and 30 min.
The ballet classes consists in barre work and center work with specific ballet exercises.
|
Other: Ballet Group
Ballet Classes three times a week, totaling 24 sessions.
|
The intervention is ballet classes three times a week, 1 hour and 30 min.
The ballet classes consists in barre work and center work with specific ballet exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The change in turnout
Time Frame: One week before the first session of the intervention and 12 weeks after the intervention
|
Turnout is determined as external rotation of the coxofemoral joint, and is considered perfect when reaching an angle of 180 ° between the longitudinal axis of the feet.
The change in turnout will be evaluated one week before the first session of the intervention and after 12 weeks of Mat Pilates training.
So, the primary outcome is the change in the range of ballerinas' turnout.
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One week before the first session of the intervention and 12 weeks after the intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- de Leva P. Adjustments to Zatsiorsky-Seluyanov's segment inertia parameters. J Biomech. 1996 Sep;29(9):1223-30. doi: 10.1016/0021-9290(95)00178-6.
- Gilbert CB, Gross MT, Klug KB. Relationship between hip external rotation and turnout angle for the five classical ballet positions. J Orthop Sports Phys Ther. 1998 May;27(5):339-47. doi: 10.2519/jospt.1998.27.5.339.
- Koutedakis Y, Sharp NC. Thigh-muscles strength training, dance exercise, dynamometry, and anthropometry in professional ballerinas. J Strength Cond Res. 2004 Nov;18(4):714-8. doi: 10.1519/13983.1.
- van Merkensteijn GG, Quin E. Assessment of Compensated Turnout Characteristics and their Relationship to Injuries in University Level Modern Dancers. J Dance Med Sci. 2015 Jun;19(2):57-62. doi: 10.12678/1089-313X.19.2.57.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2017
Primary Completion (Actual)
August 30, 2017
Study Completion (Actual)
July 31, 2018
Study Registration Dates
First Submitted
December 7, 2017
First Submitted That Met QC Criteria
December 14, 2017
First Posted (Actual)
December 19, 2017
Study Record Updates
Last Update Posted (Actual)
April 25, 2019
Last Update Submitted That Met QC Criteria
April 24, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- TURN1217
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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