The Greek Acute Dance Injuries Registry (GrADIR)

January 24, 2024 updated by: Michail Elpidoforou, National and Kapodistrian University of Athens

Systematic Registration and Longitudinal Monitoring of Predisposing Factors and Acute/Emergent Events of Higher Vocational Schools' Students.

Dance is a highly demanded physical activity with a high rate of acute and emergent events (AEE). No systematic prospective study has been conducted in any Greek population of dance students for the registration of the AEE and their possible predisposing factors. This is a prospective cohort study, the purpose of which is to register the AEE risk factors, their long-term follow-up, and the potential AEE during an academic year in adult dance students in Athens, Greece.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

Dance, as a physical activity, is considered as one of the most demanding activities at a young age with a high rate of acute and emergent events (AEE). Although dancers perform movement combinations that require high athletic ability, often their physical fitness levels appear to be unexpectedly low and the majority of them will experience at least one injury a year. Determination of the AEE predisposing factors in dancers is necessary to reduce their percentage rates, and until now no systematic prospective study has been conducted in a Greek population of vocational dance schools' students to register both the AEE themselves and their possible predisposing factors.

The primary objective of the study is to register the risk factors for the AEE occurrence in students at Higher Vocational Schools of Dance in Athens and their long-term follow-up. Secondary objectives are to register potential AEE during an academic year and to investigate possible correlations of the above parameters, both among themselves and with socio-demographic, anthropometric, psychometric and medical characteristics of the sample. Finally, a translation and cross-cultural adaptation to a Greek population of the Dance Functional Outcome Survey (DFOS) scale will be carried out.

This is a prospective cohort study with the study population being adult students of 8 Higher Vocational Schools of Dance in Athens. A registration of socio-demographic, anthropometric and medical characteristics, as well as an electrocardiogram, will be carried out at the beginning of the academic year. Core stabilization, balance, body composition, aerobic capacity, dance motor control, dance functional ability, quality of life, fatigue, depressive symptoms, anxiety, stress, performance satisfaction, risk for developing eating disorders, athletic burnout, and predisposition to psychological flow will be registered at the beginning and at the end of the academic year.

Study Type

Observational

Enrollment (Estimated)

300

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

    • Attiki
      • Chaïdári, Attiki, Greece, 12462
        • Michail Elpidoforou

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

All the undergraduate students of the eight higher vocational dance schools in Athens-Greece, that participate in the study, they are going to be informed that they could be indorsed in the study according to the aforementioned inclusion and exclusion criteria.

Description

Inclusion Criteria:

  • Undergraduate student in one of the eight Higher Vocational Dance Schools of the study
  • Age ≥18 years
  • Ability to understand, write and speak Greek
  • Written consent for participating into the study

Exclusion Criteria:

  • Student listener who is not officially participating to the whole educational program
  • Pregnancy
  • Deny to participate and/or give a written consent for participating into the study

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
Greek National School of Dance - GNSD
All the GNSD undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School of Maria Grigoriou - Choros
All the Choros undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School Chorochronos
All the Chorochronos undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School of Moragemou
All the Moragemou undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School Aktina
All the Aktina undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School of Maro Marmarinou
All the Maro Marmarinou undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School of Athens Conservatoire
All the Athens Conservatoire undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.
Higher Vocational Dance School of Marias Chatzimihali Charlafti
All the Marias Chatzimihali Charlafti undergraduate students with written consent for participating into the study
Classes, Rehearsals, and Performances of classical ballet and contemporary dance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Registration of Possible Acute/Emergent Events (AEE)
Time Frame: Weekly during one 8-month academic year.
Undergraduate dance students will be asked to report any of their AEE (prevalence and body region), including any acute and/or emergent dysfunction of a tissue/organ which will be lead to at least one day off from any dance activity, and the AEE mechanism during all the weeks of the academic year.
Weekly during one 8-month academic year.
Acute/Emergent Events (AEE) Incidence Rates
Time Frame: AEE incidence rates will be calculated over the 8-month prospective follow-up.
AEE incidence rates will be calculated per 1000 dance exposures (dance classes, rehearsals, and performances), according to past research [(number of AEE/dance exposures)*1000] (Dang et al, 2020).
AEE incidence rates will be calculated over the 8-month prospective follow-up.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of Anatomical Variations (AV)
Time Frame: Baseline
All the participants will be assessed by a registered physiotherapist either positively (incidence of the AV) or negatively (non-incidence of the AV) for the following AV: knee valgus, knee varum, hallux valgus, splay foot, forefoot adduction, hindfoot varum, hindfoot valgus, longitudinal arch cavus, longitudinal arch planus, forward head, cervical lordosis, thoracic kyphosis, scoliosis, lumbar lordosis, and knee hyperextension, according to past publications (Gamboa et al, 2008; Steinberg et al, 2012).
Baseline
Registration of subscales score of Medical Outcome Study 36-Item Short-Form Health Survey (SF-36)
Time Frame: Baseline, after 8 weeks, and over the 8-month prospective follow-up.
SF-36 is used to assess Quality of Life (QoL) and consists of eight physical and mental health domains: Physical Functioning (PF), Role Physical (RP), Bodily Pain (BP), General Health (GH), Vitality (VT), Social Functioning (SF), Role Emotional (RE), and Mental Health (MH). Subscales evaluate health between 0 and 100, and 0 indicates "bad health", 100 indicates "good health". It will be used to assess QoL and to study construct validity of the DFOS-Gr, similar to that tested in the english (Bronner and Urbano, 2018), spanish (de-la-Cruz-Torres et al, 2020), and italian (Contri et al, 2021) version.
Baseline, after 8 weeks, and over the 8-month prospective follow-up.
Beighton hypermobility score
Time Frame: Baseline
Beighton-score is 9 point score for the assessment of hypermobility. It investigates the presence of hyperlaxity (yes = 1, no = 0) at both wrists, the fifth metacarpo-phalangeal joints, elbows, knee joints, and the lumbosacral joints. Sum of the items ranges from 0 to 9 points, with higher scores indicating greater joint laxity.
Baseline
Thomas Test (TT)
Time Frame: Baseline
TT (also known as Iliacus Test or Iliopsoas Test) is used to measure hip flexors (iliopsoas muscle group, rectus femoris, pectineus, gracillis, tensor fascia latae, and sartorius) flexibility. Participants will be assessed by a registered physiotherapist either positively (non-flexible hip flexors) or negatively (flexible hip flexors) from supine position on the examination table. Participant holds one knee flexed on his/her chest and lowers the tested limb toward the table. Test is positive when the tested hip joint is flexed, and negative when is hyperextended with the tested limb's thigh under the table.
Baseline
Active Straight Leg Raise (SLR)
Time Frame: Baseline
SLR is used to measure hamstring (semimembranosus, semitendinosus and biceps femoris) flexibility. Participants will be assessed by a registered physiotherapist either positively (non-flexible hip flexors) or negatively (flexible hip flexors) from supine position on the examination table. Participant actively flexes his tested hip joint with the knee extended and the non-tested limb totally extended on the table. Test is positive when the tested hip joint is flexed more than 90 degrees, and negative when it is flexed less than 90 degrees.
Baseline
Ober Test (OT)
Time Frame: Baseline
OT is used to measure tensor fascia latae (TFL) flexibility. Participants will be assessed by a registered physiotherapist either positively (non-flexible TFL) or negatively (flexible TFL) from lateral decubitus position. The evaluator flexes the knee of the tested limb at 90 degrees and abducts and extends the hip until it is level with the trunk. Only gravity then acts to the tested hip joint bringing it on the maximum possible passive adduction. Test is positive when tested limp's knee is off the table, and negative when it is on the table.
Baseline
Electrocardiogram (ECG)
Time Frame: Baseline
For the registration of the prevalence of possible cardiac clinical signs, an ECG will be executed and clinically interpreted by a registered cardiologist.
Baseline
Dance-related Flexibility Assessment
Time Frame: Baseline
Five assessments with a goniometer in both sides will be executed, according to past research (Yin et al, 2019): passive range of dorsiflexion from supine position, passive range of hip external and internal rotation from prone position, passive range of hip horizontal abduction from supine position, and active range of hip external rotation from standing position (first feet ballet position), with higher ranges of motion indicating greater flexibility.
Baseline
Prone Plank Test
Time Frame: Baseline and over the 8-month prospective follow-up.
The participant is asked to lie facing down and rise on their elbows and toes while keeping the body in a straight line. The total time is recorded for the assessment of the core region muscles strength and endurance (more often called as "core stability"). The time is stopped if the participant lowers or lifts his/her body.
Baseline and over the 8-month prospective follow-up.
Side Plank Test
Time Frame: Baseline and over the 8-month prospective follow-up.
The participant is asked to lie on his/her side on the elbow with the lower limbs in full extension. Participant is asked to lift the lower limbs so that the hips and back are aligned and mentain this position. The total time is recorded for both sides, right and left, for the assessment of the lateral trunk flexor muscles strength and endurance (more often called as "lateral core stability"). The time is stopped if the participant lowers or lifts his/her pelvis.
Baseline and over the 8-month prospective follow-up.
Stork Balance Stand Test
Time Frame: Baseline and over the 8-month prospective follow-up.
The participant is asked to stand on one foot while he/she raises the other foot off the floor. The total time is recorded for both sides, right and left, for the assessment of static balance. The time is stopped if the supported foot is moved away from the starting position and/or the non-supported foot touches the floor. Rahman's et al (2017) categorization will be used: great (>50''), good (40''-50''), typical (25''-39''), acceptable (10''-24''), and poor (<10'') balance.
Baseline and over the 8-month prospective follow-up.
Bioelectrical Impedance (BI) assessment
Time Frame: Baseline and over the 8-month prospective follow-up.
BI will be used to assess body mass (kg), body mass index - BMI (kg/cm^2), fat mass (percentage), and muscle mass (kg).
Baseline and over the 8-month prospective follow-up.
Accelerated Step Test (AST)
Time Frame: Baseline and over the 8-month prospective follow-up.
AST is a variation of Kasch Step Test for the aerobic capacity evaluation. Participant is asked to step up and down on a 0,305 meter step for 3 minutes following an audible metronome adjusted in 112 beats*min^-1. Resting heart rate (RHR) before the test and Heart Rate Recovery (HRR) one minute after the test finish will be assessed. HRR score closer to RHR score indicates greater aerobic capacity, according to Darr et al (1988).
Baseline and over the 8-month prospective follow-up.
Dance Technique Screening Instrument (DTSI)
Time Frame: Baseline and over the 8-month prospective follow-up.
DTSI is a dance-specific motor control instrument, which assesses the dancer's motor control for different body regions during the execution of 3 dance movements: grand plié à la seconde [pelvis, hips, knees, and feet (0-4 points)], dèveloppé à la seconde [pelvis, turn-out, hips, knees, feet (0-5 points), and sautés au premier position [pelvis, hips, knees, feet (0-4 points)]. One point is added for each incorrect body region's execution. A total score from 9 to 13 points indicates a poor technique, from 5 to 8 points indicates a moderate technique, and from 0 to 4 points indicates a good technique.
Baseline and over the 8-month prospective follow-up.
Dance Functional Outcome Survey (DFOS)
Time Frame: Baseline, after 8 weeks, and over the 8-month prospective follow-up.
DFOS is a 14-item lower extremity and low back likert-scale questionnaire, which assesses dancer's ability to accomplish activities of daily living (ADL) and dance-specific movements. It has 2 subscales; the first consists of six items regarding ADL and scored with a total of 40 points, and the second consists of eight items regarding technique and scored with a total of 50 points. The DFOS-total is both sections combined, for a possible score of 90 points, and it is multiplied by 100 to be normalized to a percentage (Bronner et al, 2019).
Baseline, after 8 weeks, and over the 8-month prospective follow-up.
Multidimensional Fatigue Inventory (MFI)
Time Frame: Baseline and over the 8-month prospective follow-up.
MFI is a 20-item instrument to measure five dimensions of fatigue (general fatigue, physical fatigue, reduced activity, reduced motivation, and mental fatigue), each item is scored from one to five and each dimension consists of five items. The dimensional score consequently ranges from 4 to 20 (a higher score indicates more fatigue).
Baseline and over the 8-month prospective follow-up.
Depression Score in Depression, Anxiety and Stress Scale 21 (DASS-21)
Time Frame: Baseline and over the 8-month prospective follow-up.
Normal score: 0-9, Mild score: 10-12, Moderate score: 13-20, Severe score: 21-27, and Extremely severe: 28-42.
Baseline and over the 8-month prospective follow-up.
Anxiety Score in Depression, Anxiety and Stress Scale 21 (DASS-21)
Time Frame: Baseline and over the 8-month prospective follow-up.
Normal score: 0-6, Mild score: 7-9, Moderate score: 10-14, Severe score: 15-19, and Extremely severe: 20-42.
Baseline and over the 8-month prospective follow-up.
Stress Score in Depression, Anxiety and Stress Scale 21 (DASS-21)
Time Frame: Baseline and over the 8-month prospective follow-up.
Normal score: 0-10, Mild score: 11-18, Moderate score: 19-26, Severe score: 27-34, and Extremely severe: 35-42.
Baseline and over the 8-month prospective follow-up.
Performance Satisfaction Scale (PSS)
Time Frame: Baseline and over the 8-month prospective follow-up.
PSS is a 1-item likert-scale questionnaire to assess the level of dance performance satisfaction, as it is used in past studies (Dotti et al, 1998; Yannakoulia et al, 2004). Total score ranges from 1 (i am not satisfied at all) to 10 (i am absolutely satisfied).
Baseline and over the 8-month prospective follow-up.
Eating Attitudes Test (EAT-26)
Time Frame: Baseline and over the 8-month prospective follow-up.
The EAT-26 is a 26-item scale. Items are presented in a 6-point Likert-scale ranging from 1 ("never") to 6 ("always). The total score is obtained re-coding scores as follows: scores from 1 to 3 are re-coded as 0, 4 is re-coded as 1, 5 as 2, and 6 is recoded as 3. The only exception is item 25 whose answers score as follows: 1 as 3, 2 as 2, 3 as 1, and 4 to 6 as 0. The EAT-26 total score ranges from 0 to 78. A higher score indicates greater levels of attitudes and behaviors related to eating disorders.
Baseline and over the 8-month prospective follow-up.
Athlete Burnout Questionnaire (ABQ)
Time Frame: Baseline and over the 8-month prospective follow-up.
Greek version of ABQ is a 13-item scale that evaluates the 3 constructs of athlete burnout: emotional or physical exhaustion, reduced sense of accomplishment, and sport devaluation. Each item is rated on a 5-point Likert scale ranging from almost never (1) to almost always (5). To calculate average scores for each construct of athlete burnout, subscale scores were summed individually and divided by 5. Higher scores indicate higher burnout levels.
Baseline and over the 8-month prospective follow-up.
Dispositional Flow Scale-2 (DFS-2)
Time Frame: Baseline and over the 8-month prospective follow-up.
DFS-2 is a 36-item scale of a 5-point Likert-scale questionnaire ranges from 1 (totally disagree) to 5 (totally agree), with four items for each one of the following nine components (also known as factors and dimensions): Challenge-Skill Balance (CSB), Merging of Action-Awareness (MAA), Clear Goals (CG), Unambiguous Feedback (UF), Concentration on Task at Hand (CTH), Sense of Control (SC), Loss of Self-Consciousness (LSC), Transformation of Time (TT), and Autotelic Experience (AE).
Baseline and over the 8-month prospective follow-up.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Michail Elpidoforou, MSc, Department of Emergency Medicine, Attikon University Hospital

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

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 10, 2021

Primary Completion (Actual)

September 17, 2021

Study Completion (Estimated)

July 31, 2025

Study Registration Dates

First Submitted

January 14, 2024

First Submitted That Met QC Criteria

January 14, 2024

First Posted (Actual)

January 24, 2024

Study Record Updates

Last Update Posted (Estimated)

January 26, 2024

Last Update Submitted That Met QC Criteria

January 24, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 285/10.05.2023

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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