NCT07589218

Brief Summary

This research aims to complement existing podiatric studies by providing information on the relationship between ligamentous hyperlaxity, a benign condition more frequently found in the pediatric population, and ankle range of motion in child basketball players aged 8-15. Furthermore, this hyperlaxity will allow us to correlate it with the most frequent type of injury experienced by the participants and assess whether future research could develop a prevention plan for this population and extrapolate it to more professional categories.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for all trials

Timeline
0mo left

Started Dec 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress96%
Dec 2025May 2026

Study Start

First participant enrolled

December 9, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

March 14, 2026

Completed
2 months until next milestone

First Posted

Study publicly available on registry

May 15, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2026

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2026

Expected
Last Updated

May 15, 2026

Status Verified

May 1, 2026

Enrollment Period

5 months

First QC Date

March 14, 2026

Last Update Submit

May 13, 2026

Conditions

Keywords

ankleoctobalancestargazing testdorsiflexionhypermobilityrange of movementdynamic balancemovement quality

Outcome Measures

Primary Outcomes (4)

  • "Ankle Test" with Leg Motion® (Check Your Motion®, Albacete, Spain)

    Validated to numerically quantify ankle dorsiflexion, it provides very low levels of interobserver bias (ICC values ranged from 0.96 to 0.98)

    Baseline

  • Easy Angle digital inclinometer

    It was used to obtain data on the inclination of the tibia relative to the ground, measured from the tibial tuberosity or 15 cm below it. It was also used to complete the Beighton scale in the ranges of finger, elbow, and knee hyperextension because it can function as a simple goniometer.

    Baseline

  • "Lower Body Test" at Octobalance (Check Your Motion®, Albacete, Spain)

    Considered innovative for the information it provides to prevent injuries, this patented system allows us to see limb imbalances, joint restrictions such as those in the ankle, and evaluate the quality of movement during dynamic balance.

    Baseline

  • Beighton Scale

    The most widely used tool for measuring generalized hypermobility in the healthcare field. Parameters used in this population have been measured using units from 0 to 9.

    Baseline

Study Arms (2)

Hypermobile group (H+)

Children playing basketball with ligamentous hyperlaxity

Non-hypermobile group (H-)

Children who play basketball and do not suffer from ligamentous hyperlaxity

Eligibility Criteria

Age8 Years - 15 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

The study population will consist of male basketball players from the Puerto de Sagunto Basketball Club. The subjects who will participate in the study will be those who volunteer and meet the established selection criteria. The sample will include basketball players from the following age categories: U12 (8-10 years), U14 (10-12 years), and U16 (13-15 years).

You may qualify if:

  • Subjects within the age range specified in the study.
  • Signed and fully completed parental consent form.
  • Participation in basketball as a sport twice a week, not including school physical education, or a total of 3 hours per week.

You may not qualify if:

  • Subjects with injuries or any musculoskeletal impairment relevant to the measurement of the parameters to be evaluated.
  • Any temporary illness that prevents the participant from being in full physical condition.
  • Disorders related to loss of balance due to vestibular, cognitive, or cerebellar causes.
  • Performance of a warm-up outside of the established protocol.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Facultad de Medicina y Ciencias de la Salud - Universidad Católica de Valencia

Valencia, Valencia, 46001, Spain

RECRUITING

Study Officials

  • Benjamín Cuenca Valero, Doctor en Podología

    C/ Quevedo, 2, 46001 Ciutat Vella, Valencia - Facultad de Medicina y Ciencias de la Salud - Universidad Católica de Valencia

    STUDY DIRECTOR
  • Carlos Sales Castellanos, Podología y Fisioterapia

    C/ Quevedo, 2, 46001 Ciutat Vella, Valencia - Facultad de Medicina y Ciencias de la Salud - Universidad Católica de Valencia

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Carlos Sales Castellanos, Podología y Fisioterapia

CONTACT

Benjamín Cuenca Valero, Doctor en Podología

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

March 14, 2026

First Posted

May 15, 2026

Study Start

December 9, 2025

Primary Completion

May 15, 2026

Study Completion (Estimated)

May 30, 2026

Last Updated

May 15, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will share

When they formally request it

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
Once the study is completed and indefinitely
Access Criteria
Requesting it from the IP formally

Locations