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Plantar Pressure and Pain in Young Adults

1 maggio 2026 aggiornato da: Mehmet Burak UYAROĞLU, Fenerbahce University

Investigation of the Relationship Between Plantar Pressure Distribution and Pain Localization and Severity in Young Adults

The musculoskeletal system represents a holistic movement organization emerging from the integrated function of the central nervous system, musculoskeletal structures, and joint complexes. This organization is defined in the literature as the kinetic chain, characterized by the sequential and coordinated activation of body segments to enable distal segments to perform activities with optimal speed, position, and timing. The efficiency of the kinetic chain depends on optimal length-tension relationships, neuromuscular control, and balanced load transfer between segments. As the initial point of contact with the ground, the foot functions not merely as a passive support surface but as a dynamic structure actively involved in postural control, balance, and the regulation of ground reaction forces. Plantar pressure distribution and Center of Pressure (CoP) dynamics are considered objective indicators of foot-ground interaction. Due to its complex anatomical and biomechanical structure, any mechanical disturbance within the foot can influence the loading patterns of the entire kinetic chain.Abnormal plantar pressure distribution-characterized by increased peak pressures, altered forefoot-rearfoot load ratios, and increased CoP variability-may lead to compensatory load redistribution in proximal joints. These compensations have been associated with altered motor strategies, reduced neuromuscular control, and impaired shock absorption. Consequently, such alterations may contribute to the development of pain in proximal regions. This suggests a potential association between plantar pressure patterns and pain localization and severity in young adults.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

The musculoskeletal system is a complex and integrated structure in which movement emerges through the coordinated interaction of the central nervous system, musculoskeletal components, and joint complexes. This coordinated system is commonly conceptualized as the kinetic chain, which refers to the sequential and synchronized activation of body segments to allow distal segments to perform functional tasks with optimal timing, velocity, and alignment. The effectiveness of the kinetic chain is strongly influenced by biomechanical and neuromuscular factors, including optimal length-tension relationships, efficient neuromuscular control, and the balanced transfer of forces across interconnected segments.

Within this system, the foot represents the first point of contact with the ground and plays a crucial role in both static and dynamic conditions. Rather than acting as a passive structure, the foot functions as an active and adaptive component responsible for maintaining postural control, regulating balance, and modulating ground reaction forces. Plantar pressure distribution and Center of Pressure (CoP) parameters are widely accepted as objective measures reflecting the interaction between the foot and the ground. These parameters provide insight into load distribution patterns, stability, and movement strategies during both standing and gait.

The anatomical and functional complexity of the foot contributes to its role as a highly integrated biomechanical system. The presence of multiple bones, joints, ligaments, and muscles-many of which span more than one joint-enables the foot to adapt to varying mechanical demands. However, this complexity also makes the system susceptible to dysfunction. Any mechanical alteration within the foot, such as changes in plantar pressure distribution, can disrupt normal load transmission and consequently affect the entire kinetic chain.

Abnormal plantar pressure distribution is typically characterized by increased peak pressure values, altered forefoot-to-rearfoot load ratios, and increased variability in CoP movement. These changes may indicate inefficient load absorption and distribution during both static stance and dynamic activities such as walking. As a result, compensatory mechanisms may develop in proximal segments, including the knee, hip, and lumbar spine, in order to maintain functional movement and stability.

Previous studies have demonstrated that individuals experiencing musculoskeletal pain, particularly in the lower back, exhibit altered plantar pressure patterns during standing and walking compared to healthy individuals. These alterations are often interpreted as adaptive motor strategies aimed at minimizing discomfort. However, while such compensations may provide short term benefits, they may lead to long-term negative consequences, including disrupted muscle activation patterns, reduced neuromuscular control, and decreased efficiency in shock absorption. The cumulative effect of these alterations can result in impaired static and dynamic stability, further exacerbating abnormal loading patterns within the foot. This creates a cyclical process in which changes in plantar pressure distribution contribute to proximal dysfunction, which in turn reinforces abnormal movement patterns. Consequently, disturbances originating at the distal level may have significant implications for the entire kinetic chain. Understanding the relationship between plantar pressure distribution and pain characteristics is therefore of clinical importance. The use of pain mapping techniques in conjunction with plantar pressure analysis may provide valuable insights into how specific pressure patterns relate to localized pain regions. Such findings could support the development of targeted rehabilitation strategies aimed at optimizing load distribution, improving neuromuscular control, and reducing pain. In this context, investigating the association between plantar pressure distribution and pain localization and severity in young adults may contribute to a better understanding of biomechanical and neuromuscular factors underlying musculoskeletal pain, ultimately informing both preventive and therapeutic approaches.

Tipo di studio

Osservativo

Iscrizione (Stimato)

53

Contatti e Sedi

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

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

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

Accetta volontari sani

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Participants will be recruited using a convenience sampling method from the local population, primarily consisting of university students and their peers.

Descrizione

Inclusion Criteria:

  • Young adults aged between 18 and 35 years
  • Ability to stand and walk independently
  • Adequate cognitive function to understand and follow the measurement procedures
  • Willingness to participate voluntarily and provide written informed consent
  • Absence of acute lower extremity pain or injury on the day of assessment
  • Not using any assistive devices (e.g., orthoses, canes) during measurement

Exclusion Criteria:

  • History of a foot deformity diagnosed during childhood
  • History of musculoskeletal injury involving the lower extremity or lumbar region within the past 12 months
  • Previous surgery involving the lower extremity or lumbar region
  • Any condition that may affect general motor function, balance, circulation, sensory function, or pain perception

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
Intervento / Trattamento
Singolo Gruppo
Plantar pressure measurements will be performed using a pedobarography system. Both static and dynamic assessments will be conducted using the device.In addition, age, height, and body weight will be recorded, and body mass index (BMI) will be calculated based on these measurements. Participants' commonly used footwear type, pain localization, and pain intensity will also be assessed.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Plantar Pressure Measurement
Lasso di tempo: Baseline
Plantar pressure measurements will be performed using a pedobarography system (GHF550 Foot Checker). The device includes a 480 × 480 mm sensor platform with 2304 sensors and a sampling frequency of up to 60 Hz. Assessment of static and dynamic plantar pressure parameters using a pedobarography system, including pressure distribution, load characteristics, contact area, and related biomechanical variables.
Baseline
Pain İntensity
Lasso di tempo: Baseline
Pain intensity will be assessed using the Visual Analog Scale (VAS). Participants will be asked to rate their current pain level on a 10-cm horizontal line, where 0 indicates "no pain" and 10 indicates "worst imaginable pain." Pain localization will also be recorded based on participant self-report.
Baseline

Collaboratori e investigatori

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

Investigatori

  • Direttore dello studio: Mehmet Burak Uyaroğlu, Fenerbahçe University
  • Cattedra di studio: Yeliz Çırak, Fenerbahçe University
  • Investigatore principale: Gizem Demir Uzun, Fenerbahçe University
  • Investigatore principale: Berfu Özdemir, Fenerbahçe University

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 (Stimato)

1 maggio 2026

Completamento primario (Stimato)

1 maggio 2026

Completamento dello studio (Stimato)

1 maggio 2026

Date di iscrizione allo studio

Primo inviato

23 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 maggio 2026

Primo Inserito (Effettivo)

6 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • Fenerbahce

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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