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Development of Ergonomic Recovery Footwear Based on Foot Somatology and Biomechanics: Focusing on the Prevention of Diabetic Foot Ulcers

Development of ergonomic recovery footwear based on foot somatology and biomechanics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011575
Enrollment
80
Registered
2026-02-05
Start date
2023-06-27
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(Non-medical footwear) : 1. Pre-survey for footwear user needs (Phase 1): A preliminary survey was conducted to identify user needs and inform prototype design. Up to 60 adults (men and women) a

Sponsors

Seoul National University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Group 1 - Men and women aged =20 years. - Individuals who have experienced discomfort or functional limitations in foot function and mobility since the onset/diagnosis of diabetes. - Able to complete the survey in person or remotely (online). 2. Group 2 - Healthy men aged 20–30 years. - No history or evidence of neuromuscular disorders affecting the foot, lower extremity, or other body regions. - Medically able to participate in approximately 2 hours of low-intensity physical testing (e.g., walking and balance tasks) without health-related concerns. 3. Group 3 - Male participants aged 50 to 70 years. - Individuals with a clinical history of Diabetes Mellitus who currently have no foot complications, such as ulcers, infections, or open wounds. - Participants must have a Linear Foot Length of 265 ± 5 mm or habitually wear a shoe size of 265–270 mm. * Definition: Linear Foot Length is defined as the straight-line distance from the posterior-most point of the heel to the tip of the longest toe. - Individuals capable of continuous gait on a treadmill. (The protocol involves approximately 60 minutes of total walking: 6 sessions × 10 minutes each). - Participants must have no underlying health issues that would prevent them from participating in approximately 2 hours of low-intensity exercise (e.g., static standing, walking). - Upon selection, the individual must be able to strictly adhere to the predetermined experimental schedule.

Exclusion criteria

Exclusion criteria: * Common to All Groups - Direct affiliation with the research team: Students currently supervised by the Principal Investigator (PI) or researchers affiliated with the same laboratory/department. - Foot-related complications or deformities: Individuals with active foot wounds, ulcers, or structural deformities that cause difficulty in wearing standardized footwear. - Mobility impairment or health vulnerability: Health-vulnerable individuals who have difficulty walking or are unable to perform continuous gait on a treadmill. - Researcher’s discretion: Any other individuals deemed unsuitable for participation by the researcher for safety or study integrity reasons.

Design outcomes

Primary

MeasureTime frame
Maximum Plantar Pressure (MPP), Average Plantar Pressure (APP), and Plantar Pressure Distribution across specific anatomical regions of the foot.

Secondary

MeasureTime frame
Plantar pain during walking, subjective comfort, perceived fit, and ease of donning and doffing.

Countries

Korea, Republic of

Contacts

Public ContactYoungYoon BAE

Seoul National University

yuni0925@snu.ac.kr+82-2-880-8763

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 15, 2026