Plantar Pressure and Pain in Young Adults

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-35
SponsorFenerbahce University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial population

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

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Plantar Pressure Measurement

    Other intervention

    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.

Treatment groups

53 Participants
are divided into 1 treatment group
Group A: Single Group1 intervention

Trial outcomes

Primary outcomes

1

Plantar Pressure Measurement

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.

Time frame
Baseline
2

Pain İntensity

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.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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