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Plantar Pressure and Pain in Young Adults

1 de maio de 2026 atualizado por: 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.

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Descrição detalhada

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 de estudo

Observacional

Inscrição (Estimado)

53

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Método de amostragem

Amostra Não Probabilística

População do estudo

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

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
Grupo único
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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Plantar Pressure Measurement
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Diretor de estudo: Mehmet Burak Uyaroğlu, Fenerbahce University
  • Cadeira de estudo: Yeliz Çırak, Fenerbahce University
  • Investigador principal: Gizem Demir Uzun, Fenerbahce University
  • Investigador principal: Berfu Özdemir, Fenerbahce University

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de maio de 2026

Conclusão Primária (Estimado)

1 de maio de 2026

Conclusão do estudo (Estimado)

1 de maio de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

23 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de maio de 2026

Primeira postagem (Real)

6 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • Fenerbahce

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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