- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05500131
The Association Between Restricted Ankle Joint Dorsiflexion and Dynamic Knee Valgus (TOBROD)
The Association Between Restricted Ankle Joint Dorsiflexion and Dynamic Knee Valgus in Non-injured Youth Federated Basketball Players: a Cross-sectional Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Cross-sectional study. Ankle dorsiflexion range of motion was assessed by the Weight-bearing lunge test and the dynamic knee valgus by the Single leg squat test.
The participants were basketball players who belonged to youth basketball de-velopmental teams in the under-12 (U12), under-14 (U14), under-16 (U16) and under-17 (U17) categories. All participants were recruited by means of simple random sampling from the Catalan Basketball Federation during the 2018-2019 season. The participants were classified according to gender and age as stipulated by the rules determined an-nually for the respective official competitions. The study was carried out in the facilities of each club. The inclusion criteria were being age >12 and ≤17 at testing and actively competing during the study. Subjects were excluded if they had sustained any type of injury in the lower limbs before screening; presented any injury (overuse or acute) at the time of testing; if they had any oncological, psychological and/or psychiatric illnesses; or if they did not attend on the day of the assessment.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Barcelona, Spain, 08018
- Federación Catalana de Baloncesto
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being age >12 and ≤17 at testing and actively competing during the study
Exclusion Criteria:
- Subjects were excluded if they had sustained any type of injury in the lower limbs before screening; presented any injury (overuse or acute) at the time of testing; if they had any oncological, psychological and/or psychiatric illnesses; or if they did not attend on the day of the assessment.
Study Plan
How is the study designed?
Design Details
- Observational Models: Ecologic or Community
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Experimental group
All participants allowed three practice trials for each test in this order: the Weight-bearing lunge test and the Single-leg squat test.
Both of them were evaluated through the Leg Motion system (LegMotion, your MOtion®, Albacete, Spain)
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Ankle joint dorsiflexion was evaluated with the Weight-bearing lunge test through the Leg Motion system (LegMotion, your MOtion®, Albacete, Spain). Subjects were instructed to try to bring the knee to touch the metal rod (initially placed at a distance of 10 cm) without lifting the heel off the ground. The distance achieved was recorded in centimeters. Single-leg squat test was analyzed through the Leg Motion system (LegMotion, your MOtion®, Albacete, Spain). It consists of performing a monopodial squat to test dynamic knee valgus. They were to perform a single-leg squat to 30° knee flexion. The knee was considered to be aligned if the patella was over the second toe. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ankle joint dorsiflexion
Time Frame: 1 year
|
he Weight-bearing Lunge Test measured with the Leg Motion® system (Check Your Motion, Albacete) was used.
Ankle dorsiflexion was recorded in centimeters.
|
1 year
|
|
Dynamic lower extremity valgus
Time Frame: 1 year
|
The Single Leg Squat Test was used.
The evaluator recorded a frontal and sagittal view with two filming devices.
The knee was considered to be aligned if the patella was over the second toe.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Age
Time Frame: 1 year
|
Years
|
1 year
|
|
Gender
Time Frame: 1 year
|
Male or female
|
1 year
|
|
Weight
Time Frame: 1 year
|
Kilograms
|
1 year
|
|
Height
Time Frame: 1 year
|
Centimeters
|
1 year
|
|
Wingspan
Time Frame: 1 year
|
Centimeters
|
1 year
|
|
Body mass index
Time Frame: 1 year
|
Kg/m2
|
1 year
|
|
Hypermobility
Time Frame: 1 year
|
Beighton's criteria (scores of >7 points out of a total of 9 points were considered hypermobile)
|
1 year
|
|
Age categories
Time Frame: 1 year
|
According to the age of the participant could compete in 4 categories: U12, U14, U16 or U17.
|
1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 123/2018_3
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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