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Frontal Plane Knee Projection Angle and Functional Performance in Adolescent Female Volleyball Players (FPPA-DBA)

14 luglio 2026 aggiornato da: SEFA HAKTAN HATIK, Sinop University

Investigation of the Relationship Between Frontal Plane Knee Projection Angle and Dynamic Balance, Agility, and Ankle Dorsiflexion Mobility in Adolescent Female Volleyball Players

This observational study aims to examine the relationship between frontal plane knee projection angle, dynamic balance, agility performance, and ankle dorsiflexion mobility in adolescent female volleyball players. Frontal plane knee projection angle will be assessed during a single-leg squat using two-dimensional video analysis. Dynamic balance will be evaluated with the Lower Quarter Y-Balance Test, agility with the T-Test, and ankle dorsiflexion mobility with the Weight-Bearing Lunge Test.

All measurements will be completed in a single session under standardized field conditions, and no intervention or experimental treatment will be applied. By investigating how frontal plane knee alignment is associated with functional performance measures, this study may help improve the understanding of biomechanical factors related to movement quality and injury risk in adolescent female volleyball players.

Panoramica dello studio

Descrizione dettagliata

This observational, cross-sectional study aims to investigate the relationship between frontal plane knee projection angle (FPPA), dynamic balance, agility performance, and ankle dorsiflexion mobility in adolescent female volleyball players. Volleyball is a sport that requires repeated jumping, landing, lateral movements, and rapid changes of direction, which place considerable biomechanical demands on the lower extremities. In adolescent female athletes, lower-limb movement patterns may be influenced by growth, maturation, and neuromuscular control, making this population important for biomechanical assessment.

The primary study variable will be frontal plane knee projection angle, assessed during a single-leg squat using two-dimensional video analysis. Secondary measures will include dynamic balance assessed with the Lower Quarter Y-Balance Test, agility assessed with the T-Test, and ankle dorsiflexion mobility assessed with the Weight-Bearing Lunge Test. All assessments will be completed in a single session under standardized field conditions. No intervention, treatment, or experimental exercise program will be applied.

The study is designed to explore whether frontal plane knee alignment is associated with functional performance measures in adolescent female volleyball players. A better understanding of these relationships may contribute to the identification of biomechanical characteristics related to lower-extremity movement quality and potential injury risk in this population.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

70

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Ödemiş
      • Izmir, Ödemiş, Turchia (Türkiye), 35750
        • AB Volleyball Academy

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto

Accetta volontari sani

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

The study population consisted of adolescent female volleyball players aged 10 to 19 years who were regularly training at least 3 days per week at AB Volleyball Academy in Izmir, Türkiye. Only participants who had reached menarche and met all eligibility criteria were included.

Descrizione

Inclusion Criteria:

  • Being female and between 10 and 19 years of age
  • Participating in regular volleyball training at least 3 days per week
  • Having reached menarche

Exclusion Criteria:

  • Having sustained a lower extremity injury within the previous 6 months
  • Having a history of lower extremity surgery
  • Using medication that could affect balance, attention, or physical performance
  • Having a neurological, orthopedic, or systemic condition that could affect performance

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Adolescent Female Volleyball Players
Adolescent female volleyball players who were regularly training at AB Volleyball Academy and participated in this observational study. All participants completed biomechanical and functional assessments in a single session, including frontal plane knee projection angle during a single-leg squat, dynamic balance, agility, and ankle dorsiflexion mobility measurements. No intervention or experimental treatment was applied.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Frontal Plane Projection Angle
Lasso di tempo: At a single assesment sessiomn
Frontal plane projection angle (FPPA) was assessed using SparkMotion software. FPPA was calculated from the angle between a line from the anterior superior iliac spine (ASIS) to the midpoint of the patella and a line from the patellar midpoint to the midpoint between the medial and lateral malleoli; this value was subtracted from 360° to obtain FPPA. Values ≥195° were descriptively classified as increased FPPA. Frontal-plane video was recorded using an iPad mounted on a tripod positioned 3 m from the participant and 1 m above the ground. Participants performed a single-leg squat with arms crossed over the chest at a metronome-paced tempo (2 s descent, 2 s ascent). FPPA was measured at the deepest squat position reached while maintaining balance. After 3 practice trials, 5 consecutive recorded squats were performed, and the third trial was used for analysis.
At a single assesment sessiomn

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Y - Balance Test
Lasso di tempo: At a single assesment session
Dynamic balance was assessed using the Lower Quarter Y-Balance Test (YBT-LQ). This standardized test evaluates reach distance in the anterior, posteromedial, and posterolateral directions while maintaining single-leg stance. Reach distances were recorded to the nearest 0.5 cm using the Y Balance Test kit. Before testing, leg length was measured from the anterior superior iliac spine (ASIS) to the distal tip of the medial malleolus, and results were normalized to leg length. Participants completed 6 practice trials before testing, followed by 3 valid trials in each direction. Invalid trials were repeated, and the mean of the 3 valid trials for each direction was used for analysis. The composite score was calculated by dividing the sum of the 3 reach distances by 3 times leg length and multiplying by 100.
At a single assesment session
T - Test
Lasso di tempo: At a single assesment session
Agility was assessed using the T-Test. The test course was set up in a T shape with 4 cones: cone A was positioned 9.14 m from the center cone B, and cones C and D were placed 4.57 m to the left and right of cone B. Participants started at cone A, sprinted to cone B, shuffled laterally to touch cone C, then shuffled to touch cone D, returned to cone B, and backpedaled to cone A to complete the test. Time was recorded using a photocell timing system. After 2 familiarization trials, participants performed 3 valid trials with 3 minutes of rest between trials, and the best time was used for analysis.
At a single assesment session
Weight - Bearing Lunge Test
Lasso di tempo: At a single assesment session
nkle dorsiflexion mobility was assessed using the Weight-Bearing Lunge Test (WBLT). Participants were positioned facing a wall in a tandem stance, with the tested foot aligned perpendicular to the wall and the non-tested rear heel lifted. They were instructed to place their hands on the wall and move the front knee toward it while keeping the tested heel in contact with the ground. The foot was moved away from the wall in 1 cm increments until the maximum distance at which the knee could still touch the wall without heel lift was identified. The farthest valid distance between the great toe and the wall was measured in centimeters. Three valid trials were recorded for each lower extremity, and the mean value was used for analysis. Trials with heel lift, marked lower-extremity compensations, or loss of proper test position were repeated.
At a single assesment session

Collaboratori e investigatori

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Pubblicazioni e link utili

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Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 marzo 2026

Completamento primario (Effettivo)

3 marzo 2026

Completamento dello studio (Effettivo)

1 luglio 2026

Date di iscrizione allo studio

Primo inviato

14 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 luglio 2026

Primo Inserito (Effettivo)

17 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

17 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • FPPATTADF1

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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