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Lower Limb and Foot Health in Danish Paediatric Ballet Dancers and Foot-ballers

NCT07933068, Not yet recruiting, University hospital of Odense

Trial 8

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleLower Limb and Foot Health in Danish Paediatric Ballet Dancers and Foot-ballersClinicalTrials.gov
NCT numberNCT07933068ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
Enrollment148 participants, estimatedClinicalTrials.gov
Lead sponsorUniversity hospital of OdenseClinicalTrials.gov
ConditionsMusculoskeletal Health, Lower Extremity Biomechanics, Foot Health, Musculoskeletal PainClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryPassive External Hip RotationAt the single baseline study visit (cross-sectional assessment)
Passive external hip rotation will be measured in degrees using a goniometer, with the participant in the prone position, the knee flexed to 90 degrees, and the pelvis stabilized. The participant-level mean of right and left hip measurements will be used to compare ballet dancers with the age- and sex-frequency-matched reference cohort. Higher values indicate greater external hip rotation.
ClinicalTrials.gov
SecondaryAnkle Plantarflexion Range of MotionAt the single baseline study visit
Maximum passive ankle plantarflexion will be measured in degrees using a standardized clinical examination protocol. Measurements will be compared between ballet dancers and the age- and sex-frequency-matched reference cohort.
ClinicalTrials.gov
SecondaryLower Limb Rotational Profile and Joint Range of MotionAt the single baseline study visit
Clinical measurements of hip internal rotation, lower limb rotational alignment, and joint range of motion will be recorded in degrees using standardized examination procedures. Measurements will be analyzed descriptively and compared between relevant study groups.
ClinicalTrials.gov
SecondaryThree-Dimensional Foot MorphologyAt the single baseline study visit
Foot morphology will be assessed using a Volumental three-dimensional foot scanner. Measurements will include foot length, forefoot width, arch height, instep height, heel width, and other predefined foot dimensions. Bilateral measurements will be recorded.
ClinicalTrials.gov
SecondaryPain Intensity - Wong-Baker FACES Pain Rating ScaleAt the single baseline study visit
1\. Pain Intensity - Wong-Baker FACES Pain Rating Scale Description: Pain intensity will be assessed using the Wong-Baker FACES Pain Rating Scale, an age-appropriate self-reported pain assessment tool. Scores range from 0 (no pain) to 10 (worst possible pain), with higher scores indicating greater pain intensity and therefore a worse outcome. The scale consists of six faces corresponding to scores of 0, 2, 4, 6, 8, and 10.
ClinicalTrials.gov
Secondary2. Pain Intensity - Numeric Rating ScaleAt the single baseline study visit
Pain intensity will be assessed using the 11-point Numeric Rating Scale for Pain (NRS), according to the child's age and ability to self-report pain. Scores range from 0 (no pain) to 10 (worst imaginable pain), with higher scores indicating greater pain intensity and therefore a worse outcome.
ClinicalTrials.gov
Secondary3. Anatomical Location of PainAt the single baseline study visit
Description: Pain location will be assessed using a standardized body map on which participants indicate the anatomical region or regions where pain is experienced. Results will be reported as the number and percentage of participants reporting pain in each anatomical region. This is a categorical assessment without a numerical severity score.
ClinicalTrials.gov
SecondaryOxford Ankle Foot Questionnaire for ChildrenAt the single baseline study visit
4\. Foot-Related Physical Function - Oxford Ankle Foot Questionnaire for Children Description: Foot-related physical function will be assessed using the Physical domain of the Oxford Ankle Foot Questionnaire for Children (OxAFQ-C). This domain consists of six items assessing the impact of foot and ankle conditions on physical activities. Each item is scored from 0 to 4, and the summed score is transformed to a scale ranging from 0 to 100. Higher scores indicate better physical functioning and therefore a better outcome. 5\. School and Play Function - Oxford Ankle Foot Questionnaire for Children Description: School and play function will be assessed using the School and Play domain of the Oxford Ankle Foot Questionnaire for Children (OxAFQ-C). This domain consists of four items assessing the impact of foot and ankle conditions on participation in school and play activities. Each item is scored from 0 to 4, and the summed score is transformed to a scale ranging from 0 to 100. Higher
ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)