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Morton Toe and Neuromuscular Performance

8 maggio 2026 aggiornato da: Nihat Sarıalioğlu, Giresun University

Morton Toe is Associated With Faster Contractile Properties and Superior Reactive Strength in Female Football Players

This cross-sectional observational study investigated whether female football players with Morton toe morphology differ from those with normal foot morphology in neuromuscular contractile properties and kinetic performance characteristics. Morton toe is a congenital foot variation in which the second toe is longer than the first. A total of 47 female football players were classified into two groups based on bilateral foot morphology: Morton foot group (n = 24) and normal foot group (n = 23). Neuromuscular properties of the dominant vastus lateralis muscle were assessed using tensiomyography, and kinetic performance was evaluated through a 40-cm drop jump test on dual force plates. The primary outcomes were contraction time (Tc) and reactive strength index (RSI). Secondary outcomes included relaxation time, delay time, sustain time, maximal displacement, jump height, peak power normalized to body mass, and landing net peak force normalized to body mass. Multiple linear regression models adjusted for age, body mass index, and mean arch index were used to evaluate whether group differences were independent of potential confounders. This study aimed to determine whether Morton toe morphology is associated with distinct neuromuscular and kinetic performance profiles in female athletes.

Panoramica dello studio

Descrizione dettagliata

Morton toe is a congenital foot morphology characterized by a longer second metatarsal relative to the first. Although traditionally regarded as a clinical or orthopedic variation associated with metatarsal stress fractures and balance difficulties, limited evidence from sprinter populations suggests that a longer second toe may be associated with superior athletic performance. However, no previous study has examined whether Morton toe morphology is related to neuromuscular contractile properties assessed via tensiomyography or kinetic performance derived from force plate testing in a controlled group comparison design.

Participants were screened from 97 female football players. Exclusion criteria included BMI outside the 18.5-29.9 range, bilateral arch index outside the 14-29% range, inconsistent bilateral foot morphology, lower-extremity injury within the past 12 months, neurological or orthopedic conditions, performance-affecting pharmacological use, and menstruation on the measurement day. Morton toe classification was based on the palpation method described by Davidson et al. (2007) with a minimal detectable change threshold of ±0.30 mm.

All measurements were conducted during the off-season to minimize training load interference. Testing followed a standardized sequence: foot morphology assessment, tensiomyography of the dominant vastus lateralis at rest, a 15-minute warm-up, and a 40-cm drop jump test. The assessor was blinded to group classification, and statistical analysis was performed by an independent researcher on a coded dataset. Primary outcome variables (Tc and RSI) were determined a priori. Secondary outcomes were corrected for multiple comparisons using the Holm-Bonferroni method. Regression analyses were performed to assess the independence of group effects from age, body mass index, and mean bilateral arch index.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

47

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

    • Centre
      • Giresun, Centre, Turchia (Türkiye), 28100
        • Giresun University - Sports Science Faculty

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

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Female football players actively competing in organized leagues in Turkey, recruited from multiple teams during the 2025-2026 off-season period. A total of 97 players were initially screened; 47 met all eligibility criteria and were classified into Morton foot (n=24) and normal foot (n=23) groups.

Descrizione

Inclusion Criteria:

  • Active female football players with a valid sports license for the current season
  • Regular participation in training and competitive matches
  • Bilateral Morton toe morphology (Δ ≤ -0.30 mm on both feet) or bilateral normal foot morphology (Δ > +0.30 mm on both feet)
  • Body mass index between 18.5 and 29.9 kg/m²
  • Bilateral arch index between 14% and 29%
  • Voluntary participation with written informed consent

Exclusion Criteria:

  • Serious lower-extremity musculoskeletal injury within the past 12 months
  • Neurological or orthopedic disease affecting measurement procedures
  • Current use of pharmacological products affecting performance
  • Acute pain, injury, or illness on the measurement day
  • Menstruation on the measurement day (self-reported)
  • Inconsistent bilateral foot morphology classification between feet
  • Bilateral arch index below 14% (high arch) or above 29% (low arch)

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
Morton Foot Group
Female football players with bilateral Morton toe morphology, defined as a second metatarsal protrusion distance exceeding the first by more than 0.30 mm bilaterally (Δ ≤ -0.30 mm). n = 24.
Normal Foot Group
Female football players with bilateral normal foot morphology, defined as a first metatarsal protrusion distance exceeding the second by more than 0.30 mm bilaterally (Δ > +0.30 mm). n = 23.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Contraction Time (Tc)
Lasso di tempo: Single measurement session
Tensiomyographic contraction time of the dominant vastus lateralis muscle, defined as the time between 10% and 90% of maximal radial displacement (ms).
Single measurement session
Reactive Strength Index (RSI)
Lasso di tempo: Single measurement session
Jump height divided by ground contact time during a 40-cm drop jump test (m/s). The trial with the highest RSI value out of three attempts was selected for analysis.
Single measurement session

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Maximal Displacement (Dm)
Lasso di tempo: Single measurement session
Peak radial displacement of the vastus lateralis muscle belly during tensiomyographic measurement (mm).
Single measurement session
Relaxation Time (Tr)
Lasso di tempo: Single measurement session
Time from 90% to 50% of maximal displacement during the relaxation phase of tensiomyographic measurement (ms).
Single measurement session
Delay Time (Td)
Lasso di tempo: Single measurement session
Time from electrical stimulus onset to 10% of maximal displacement during tensiomyographic measurement (ms).
Single measurement session
Sustain Time (Ts)
Lasso di tempo: Single measurement session
Duration the muscle response remains above 50% of maximal displacement during tensiomyographic measurement (ms).
Single measurement session
Jump Height (JH)
Lasso di tempo: Single measurement session
Vertical jump height calculated from flight time during a 40-cm drop jump test (cm).
Single measurement session
Peak Power Normalized to Body Mass (PPI)
Lasso di tempo: Single measurement session
Peak power output normalized to body mass during a 40-cm drop jump test (W/kg).
Single measurement session
Landing Net Peak Force Normalized to Body Mass (LPF)
Lasso di tempo: Single measurement session
Peak vertical ground reaction force at landing normalized to body mass during a 40-cm drop jump test (N/kg).
Single measurement session

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

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)

10 gennaio 2026

Completamento primario (Effettivo)

15 marzo 2026

Completamento dello studio (Effettivo)

15 marzo 2026

Date di iscrizione allo studio

Primo inviato

8 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

8 maggio 2026

Primo Inserito (Effettivo)

14 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

14 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

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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