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Musculoskeletal DiseasesNCT01440153

Additional Exercise Program in Professional Dancers

A study testing Exercise Intervention and Passive Intervention in people with Musculoskeletal Diseases, run by University College of Antwerp at 1 site in Belgium.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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). Read more about this study

Who is it for?
Ages 17 to 27 yearsHealthy volunteers can take part
Conditions the study is for
Musculoskeletal Diseases
What is being tested?
Exercise Intervention and Passive Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
44 participants
Where
1 siteBelgium
Study dates
Sep 2009to Nov 2011
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 17 to 27 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

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

Who cannot join

  • No full time enrollment

Trial locations and contacts

1 site in 1 country.

Belgium1 site
  • Artesis University College

    Antwerp, 2018

Other trials in Belgium

About this study

Official title: 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.

Read more

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.

Read the 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.

Being tested
Exercise Intervention, Passive Intervention
Keywords
Dance, Injury, Physical condition, Exercise
Medical subject headings
Musculoskeletal Diseases, Wounds and Injuries, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exercise InterventionOther

    Also called Fitness, Motor control, Physical condition

    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.

  • Passive InterventionOther

    Also called stress management, education, taping, massage

    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.

Study groups in NCT01440153
Study groupRoleWhat they receive
Active InterventionExperimentalNot described
Receives: Other: Exercise Intervention
passive interventionActive comparatorNot described
Receives: Other: Passive Intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in Physical condition

    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

    Measured: Post intervention (6 months after baseline evaluation)

Secondary outcomes (4)
  1. changes in musculoskeletal injury incidence during the intervention

    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).

    Measured: during intervervention (6 months after baseline)

  2. changes in motor control

    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).

    Measured: post intervention (6 months after baseline)

  3. Changes in functional evaluation during the intervention

    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).

    Measured: Post intervention (6 months after baseline)

  4. Changes in Functional evaluation during follow up

    The same questionnaires will further be collected during the follow up period (12 and 18 months after baseline assessment)

    Measured: Folow up (till 18 months after baseline evaluation)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Sep 2011 (estimated)
  2. Study startSep 2009
  3. Primary completionAug 2011
  4. Study completionNov 2011 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
44 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01440153
Sponsor's protocol ID
UZA-DRCT-2011
Status last verified
Sep 2011
First submitted
23 Aug 2011
Last updated
26 Sep 2011
Results posted
No
Data monitoring committee
No

Publications

  • Roussel NA, Vissers D, Kuppens K, Fransen E, Truijen S, Nijs J, De Backer W. Effect of a physical conditioning versus health promotion intervention in dancers: a randomized controlled trial. Man Ther. 2014 Dec;19(6):562-8. doi: 10.1016/j.math.2014.05.008. Epub 2014 Jun 3.

    PubMed 24951437

Questions about this trial

What is this clinical trial studying?

A study testing Exercise Intervention and Passive Intervention in people with Musculoskeletal Diseases, run by University College of Antwerp at 1 site in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 26 Sep 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in Physical condition (time frame: Post intervention (6 months after baseline evaluation)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01440153, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Sep 2011; AzTrials last refreshed its copy on 28 Oct 2026.

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