Plantar Pressure and Pain in Young Adults
Investigation of the Relationship Between Plantar Pressure Distribution and Pain Localization and Severity in Young Adults
1 other identifier
observational
53
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 23, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedFirst Posted
Study publicly available on registry
May 6, 2026
CompletedMay 6, 2026
May 1, 2026
Same day
April 23, 2026
May 1, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
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.
Baseline
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.
Baseline
Study Arms (1)
Single Group
Interventions
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.
Eligibility Criteria
Participants will be recruited using a convenience sampling method from the local population, primarily consisting of university students and their peers.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fenerbahce University
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Mehmet Burak Uyaroğlu
Fenerbahce University
- STUDY CHAIR
Yeliz Çırak
Fenerbahce University
- PRINCIPAL INVESTIGATOR
Gizem Demir Uzun
Fenerbahce University
- PRINCIPAL INVESTIGATOR
Berfu Özdemir
Fenerbahce University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 23, 2026
First Posted
May 6, 2026
Study Start
May 1, 2026
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
May 6, 2026
Record last verified: 2026-05