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Morton Toe and Neuromuscular Performance

8. Mai 2026 aktualisiert von: 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.

Studienübersicht

Status

Abgeschlossen

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Tatsächlich)

47

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Centre
      • Giresun, Centre, Türkei (türkiye), 28100
        • Giresun University - Sports Science Faculty

Teilnahmekriterien

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Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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.

Beschreibung

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)

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Contraction Time (Tc)
Zeitfenster: 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)
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Maximal Displacement (Dm)
Zeitfenster: Single measurement session
Peak radial displacement of the vastus lateralis muscle belly during tensiomyographic measurement (mm).
Single measurement session
Relaxation Time (Tr)
Zeitfenster: 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)
Zeitfenster: Single measurement session
Time from electrical stimulus onset to 10% of maximal displacement during tensiomyographic measurement (ms).
Single measurement session
Sustain Time (Ts)
Zeitfenster: Single measurement session
Duration the muscle response remains above 50% of maximal displacement during tensiomyographic measurement (ms).
Single measurement session
Jump Height (JH)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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

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Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

10. Januar 2026

Primärer Abschluss (Tatsächlich)

15. März 2026

Studienabschluss (Tatsächlich)

15. März 2026

Studienanmeldedaten

Zuerst eingereicht

8. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

8. Mai 2026

Zuerst gepostet (Tatsächlich)

14. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

14. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

8. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

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Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

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