Additional Exercise Program in Professional Dancers

September 23, 2011 updated by: University College of Antwerp

Influence of an Additional Intervention Targeting Physical Fitness, Endurance and Motor Control, on Physical Condition and Musculoskeletal Injuries in Contemporary Dancers

Professional dancing requires an almost perfect control of technical skills, combined with a good physical condition. To meet the demands of choreography, dancers need an adequate aerobic endurance capacity, muscular strength as well as flexibility and motor control (Twitchett et al. 2009; Roussel et al. 2009). One could compare these requirements to those of an athlete. In contrasts to athletes, only few attention has been given to the prevention of injuries in dancers. Professional dancers are at high risk to develop musculoskeletal injuries, especially, soft tissue and overuse injuries to lower extremities and spine(Hincapié et al, 2008). Several potential risk factors for injury have been suggested, such as a reduced level of aerobic fitness, lack of muscular strength, hypermobility of the joints and altered motor control of the lumbopelvic region but no conclusive evidence exists for any of these items separately.

Applying sports science principles to dance training may improve the performances of the dancers (Twitchett et al. 2009). Dancers demonstrate low aerobic fitness and muscle strength, in contrast to the high demands. Aerobic endurance of dancers is for example comparable to healthy adults with a sedentary life style.

Fitness programs, additional to regular dance classes, have only recently been considered (Twitchett et al. 2009). The advantages of additional training in athletes is beyond questioning. Nevertheless, this concept is relatively new for dancers. On the one hand, professional dancers do not consider themselves as a sportsmen but as artists (Wyon et al, 2007). On the other hand, choreographers and dancers fear the negative influence of training on body aesthetics.

Additional fitness training could improve physical fitness & motor control and may help with stress coping during public performances. Therefore, the purpose of this randomized controlled trial is to examine whether an additional intervention to regular dance lessons influences the physical condition and musculoskeletal injury rate in professional dancers.

Study Overview

Detailed Description

Prior to participation, all subjects receive verbal and written information addressing the nature of the study. First dancers are asked to fill in a self-established medical questionnaire, the Short Form 36 questionnaire (SF-36), the Dance Functional Outcome Scale (DFOS), the Baecke questionnaire, the Pain Catastrophizing Scale (PCS) and the Tampa Scale for Kinesiofobia (TSK). After a baseline assessment, consisting of an evaluation of the physical condition (maximal exercise test, evaluation of the respiratory capacity & evaluation of explosive muscle strength using a field test), a motor control evaluation of the lumbo-pelvic region and evaluation of anthropometric measurements, the participants are randomly divided into 2 groups. They will receive an 4 months lasting intervention in addition to the regular dance lessons. The time schedule of the intervention is identical for both groups. Participants from group A receive an active program aiming at improving their cardiovascular endurance, muscular strength and motor control. The level for cardiovascular training is based on the results of the maximal exercise test performed during baseline assessment. The level of training is determined at a level of 70% of the predicted maximal heart rate and was increased every 6 weeks with 5%, ending at 85%. Heart rate will be monitored during the training.

Participants from group B will receive an alternative program, in which all active parts are replaced by passive interventions. Several education sessions will be given regarding different topics, such as stress management, nutrition, injuries, etc. In addition, also practical sessions well be held to practice massage, passive stretching, taping. The intervention will be supervised by physical therapists and master students in Physiotherapy, experienced in dancing, motor control and/or physical conditioning, and an attendance list will register the presence of the participants.

The injuries of the dancers will be registered during the intervention and during a 6 months follow up period.

Study Type

Interventional

Enrollment (Anticipated)

44

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

      • Antwerp, Belgium, 2018
        • Artesis University College

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

17 years to 27 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • students enrolled in the Bachelor of Dance at the Royal Conservatoire, Artesis Hogeschool in Lier, Belgium

Exclusion Criteria:

  • No full time enrollment

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Active Intervention
Participants from group A receive an active program aiming at improving their cardiovascular endurance, muscular strength and motor control. The level for cardiovascular training is based on the results of the maximal exercise test performed during baseline assessment. The level of training is determined at a level of 70% of the predicted maximal heart rate and was increased every 6 weeks with 5%, ending at 85%. Heart rate will be monitored during the training.
Other Names:
  • Fitness
  • Motor control
  • Physical condition
Active Comparator: passive intervention
Participants from group B will receive an alternative program, in which all active parts are replaced by passive interventions. Several education sessions will be given regarding different topics, such as stress management, nutrition, injuries, etc. In addition, also practical sessions well be held to practice massage, passive stretching, taping.
Other Names:
  • education
  • taping
  • massage
  • stress management

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Physical condition
Time Frame: Post intervention (6 months after baseline evaluation)
The physical condition is tested using an incremental exercise test on an electronically braked bicycle ergometer with a graded increase in workload. Fatigue during test performance is monitored every minute with a Borg scale from 6 (no fatigue) to 20 (complete exhaustion). There is continuous monitoring of electrocardiographic and ventilatory variables such as ventilation rate, respiration rate, VCO2 and VO2
Post intervention (6 months after baseline evaluation)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
changes in musculoskeletal injury incidence during the intervention
Time Frame: during intervervention (6 months after baseline)
A standardized questionnaire is used to collect demographic information at baseline, and an injury registration form is used to assess musculoskeletal symptoms and injuries (Cumps et al., 2007). Using this injury registration form, information is gathered about the occurrence of the symptoms and injuries, the time loss and the medical diagnosis. This injury registration form has already been used in prospective epidemiology research in sportsmen (Cumps et al., 2007) and in dancers (Roussel et al., 2009).
during intervervention (6 months after baseline)
changes in motor control
Time Frame: post intervention (6 months after baseline)
Lumbo-pelvic movement control is assessed by evaluating the subjects' ability to control movement of the lumbo-pelvic region while performing simple movements in the hips. Four commonly used clinical tests, i.e. the Active Straight Leg Raising, Bent Knee Fall Out, Knee Lift Abdominal Test and Standing Bow are used in the present study for the evaluation of lumbo-pelvic movement control. The reliability of these tests has been described elsewhere (Roussel et al. 2009a).
post intervention (6 months after baseline)
Changes in functional evaluation during the intervention
Time Frame: Post intervention (6 months after baseline)
The SF-36 is a generic instrument in which health-related quality of life is measured. The dance functional outcome questionnaire consists of two parts: daily activities and dance-related functionality. For every question there are six possible responses, ranging from 'excellent functionality' to 'poor functionality'. The DFOS has very good test-retest reliability for healthy professional dancers and is very sensitive to functional changes in the dancers (Bronner et al., 2007).
Post intervention (6 months after baseline)
Changes in Functional evaluation during follow up
Time Frame: Folow up (till 18 months after baseline evaluation)
The same questionnaires will further be collected during the follow up period (12 and 18 months after baseline assessment)
Folow up (till 18 months after baseline evaluation)

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Nathalie A Roussel, PhD, Artesis University College
  • Study Director: Wilfried De BAcker, PhD, MD, Universiteit Antwerpen

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

September 1, 2009

Primary Completion (Actual)

August 1, 2011

Study Completion (Anticipated)

November 1, 2011

Study Registration Dates

First Submitted

August 23, 2011

First Submitted That Met QC Criteria

September 23, 2011

First Posted (Estimate)

September 26, 2011

Study Record Updates

Last Update Posted (Estimate)

September 26, 2011

Last Update Submitted That Met QC Criteria

September 23, 2011

Last Verified

September 1, 2011

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UZA-DRCT-2011

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.

Clinical Trials on Musculoskeletal Diseases

Clinical Trials on Exercise Intervention

3
Subscribe