The Effect of Training on Hemodynamic Factors in Ballet Dancer

July 8, 2020 updated by: Marmara University

The Effect of Ballet Training on Plantar Venous Pump Activity in Ballerinas

Classic ballet dance is a demonstration of complex motor skills to be revealed in aesthetic combinations and repetitively, and it demands intensive use of the lower extremities within extreme of range of motion (ROM). Because ballet practice depends on advanced technical skills, it involves intensive physical training and causes an overload on the musculoskeletal system and foot deformities such as pes planus.

Plantar venous pump (PVP) is a network of multiple venous vessels located between the muscles of the foot arch. PVP is considered the first step of venous return and discharges into the posterior tibial vein (PTV). PVP is reported to be active during gait while it is inactive in resting position. There are different views on the mechanisms enabling its activation 1-3. The general view is that during the stance phase of the gait, the flattening of the plantar arch with weight transfer causes the veins in this region to narrow and creates a force that pumps the blood up.

The aim of this study is the investigation what kind of hemodynamic changes ballet training causes in the lower extremity

Study Overview

Study Type

Observational

Enrollment (Actual)

28

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

      • Istanbul, Turkey, 34000
        • Marmara University

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

14 years to 19 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Ballerinas taking ballet training at least for 4 years and female sedentary students

Description

Inclusion Criteria (for balerinas):

  • receiving ballet training at least 10 h per week for at least 4 years
  • receiving formal dancing training system

Inclusion Criteria (for non-dancer group)

  • never receiving formal dancing training
  • having sedentary lifestyle

Exclusion Criteria:

  • Participants with a history of foot or ankle surgery,
  • Participants with connective tissue disease,
  • Participants with rigid pes planus-cavus,
  • Participants with chronic venous insufficiency
  • Participants with acute ankle injury in recent 3 months

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Ballerinas
Balerina students who have trained at least for 4 years
The difference in navicular height between sitting and standing positions was recorded (mm) as the amount of navicular drop.
Venous return parameters of posterior tibial vein was measured when participant applied force equivalent to their own body weight on plantar surface of their right leg in supine position
In standing, venous return parameters was measured of posterior tibial vein when participants shift all of their weight to the right leg for 3 second with their leg muscles as relaxed as possible and their knee joint in full extension.
In standing, midfoot pressure distrubution was measured when participants shift all of their weight to the right leg
Female students
Female students with sedentary lifestyle
The difference in navicular height between sitting and standing positions was recorded (mm) as the amount of navicular drop.
Venous return parameters of posterior tibial vein was measured when participant applied force equivalent to their own body weight on plantar surface of their right leg in supine position
In standing, venous return parameters was measured of posterior tibial vein when participants shift all of their weight to the right leg for 3 second with their leg muscles as relaxed as possible and their knee joint in full extension.
In standing, midfoot pressure distrubution was measured when participants shift all of their weight to the right leg

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of navicular drop
Time Frame: Cchange from baseline navicular height in pre-intervention and immediately after the intervention/
Navicular drop was measured in mm
Cchange from baseline navicular height in pre-intervention and immediately after the intervention/
Evaluation of diameter of tibialis posterior vein in supine
Time Frame: Change from baseline diameter of tibialis posterior vein during intervention
Diameter of tibialis posterior vein was measured in mm
Change from baseline diameter of tibialis posterior vein during intervention
Evaluation of flow velocity of tibialis posterior vein in supine
Time Frame: Change from baseline flow velocity of tibialis posterior vein during intervention
Flow velocity of tibialis posterior vein was measured in cm/s
Change from baseline flow velocity of tibialis posterior vein during intervention
Evaluation of volume flow of tibialis posterior vein in supine
Time Frame: Change from baseline volume flow of tibialis posterior vein during intervention
Volume flow of tibialis posterior vein was measured in ml/min
Change from baseline volume flow of tibialis posterior vein during intervention
Evaluation of diameter of tibialis posterior vein during weight bearing
Time Frame: Change from baseline diameter of tibialis posterior during intervention
Diameter of tibialis posterior vein was measured in mm
Change from baseline diameter of tibialis posterior during intervention
Evaluation of flow velocity of tibialis posterior vein during weight bearing
Time Frame: Change from baseline flow velocity of tibialis posterior vein during intervention
Flow velocity of tibialis posterior vein was measured in cm/s
Change from baseline flow velocity of tibialis posterior vein during intervention
Evaluation of volume flow of tibialis posterior vein during weight bearing
Time Frame: Change from baseline volume flow of tibialis posterior vein during intervention
Volume flow of tibialis posterior vein was measured in ml/min
Change from baseline volume flow of tibialis posterior vein during intervention
Evaluation of midfoot plantar pressure during weight bearing
Time Frame: Change from baseline midfoot pressure during intervention
Midfoot plantar pressure was measured in gr/cm2
Change from baseline midfoot pressure during intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nilüfer Kablan, PhD, Marmara University

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.

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)

September 4, 2017

Primary Completion (ACTUAL)

November 3, 2017

Study Completion (ACTUAL)

January 5, 2018

Study Registration Dates

First Submitted

July 2, 2020

First Submitted That Met QC Criteria

July 8, 2020

First Posted (ACTUAL)

July 14, 2020

Study Record Updates

Last Update Posted (ACTUAL)

July 14, 2020

Last Update Submitted That Met QC Criteria

July 8, 2020

Last Verified

February 1, 2017

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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