- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04306068
Plyometrics in the Ankle Stabilizing Muscles in Improving Balance in Ballerinas
Efficacy of an Intervention by Plyometrics in the Ankle Stabilizers in the Improvement of the Balance in Salsa Dancers From 18 to 25 Years. A Randomized Clinical Study.
Balance is essential for successful dance performance. The effort of salsa dancers is given by the levels of stability, produced by the muscular activation of lower limbs.
The objective of the study is to assess the effectiveness of an intervention of plyometric exercises in the improvement of balance in salsa dancers from 18 to 25 years.
Randomized clinical study. 40 dancers will be randomized to the two study groups: experimental (application of plyometric exercise protocol) and control (without intervention). The treatment will last 5 weeks, with 2 weekly sessions of 25 minutes each. The dependent variables will be: equilibrium (measured with star excursion balance). The sample distribution will be calculated using the Kolmogorov-Smirnof test. The changes after each evaluation will be calculated with the t-student test. With an ANOVA of repeated measures, the intra and intersubject effect will be observed. The effect size will be obtained with Cohen's formula.
It is expected to see improvement in the stability of the ankle and the level of balance in the dancers.
Study Overview
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Comunity Of Madrid
-
Madrid, Comunity Of Madrid, Spain, 28670
- Universidad Europea de Madrid
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Dancers
- Female
- From 18 to 25 years
- With more than a year of dance practice
- And without musculoskeletal injury at the time of starting the study.
Exclusion Criteria:
- Subjects who do not attend all training sessions
- Pregnant women or intending to remain in state during the study period
- Have not signed the informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Athletes included in the experimental group will perform a plyometric exercise protocol.
Each session will consist of a 4-station circuit with 1 minute rest between each station and 30 seconds between sets
|
Each session will last 20 minutes, with 2 sessions a week, over a period of 5 weeks. The intervention will last 20 minutes, which consists of a 4-station circuit. Exercise 1: jump on the rope, with your feet together at a moderate pace. Exercise 2: In standing with hands on the hip and hip flexion (one foot in front). Knee flexion and dorsal ankle flexion, with straight trunk. Alternate legs. Exercise 3: box jump (jump on the box with both feet at the same time). Exercise 4: depth jumps from box to antoher box (jump on the box with both feet at the same time and when falling, immediately jump to the other box). 1 minute with 30 seconds between sets. |
|
No Intervention: Control group
Athletes included in the control group will follow their usual warm-up routine.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline stability after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
|
The Star excursion balance test will be used. Before performing the test, the movements will be explained. The test will be calculated in 3 directions with three tapes 140cm long and with a goniometer the subsequent sections of 135º from the previous section will be calculated, and 45º between the subsequent sections. Participants will start standing with both feet with the midpoint on the intersection mark in the center of the grid. They will be instructed to keep their hands on their hips, their heads facing forward at all times and keeping their feet flat on the floor trying to reach as far as possible in all three directions. The range will be measured by marking the tape with a pen and then measured with a measurement quote. |
Screening visit, within the first seven days after treatment and after one month follow-up visit
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DANCE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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