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Anthropometric Parameters of the Foot and Plantar Fasciitis

Examination of the Relationship Between the Anthropometric Parameters of the Foot and Plantar Fasciitis

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07151066
Acronym
PF
Enrollment
30
Registered
2025-09-03
Start date
2024-12-15
Completion date
2025-12-30
Last updated
2025-09-03

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

Conditions

Plantar Fasciitis

Keywords

Foot anthropometric measurements, Plantar Fasciitis

Brief summary

The aim of this study is to systematically evaluate anthropometric and lifestyle parameters in individuals diagnosed with PF and compare them with healthy individuals. This will reveal the structural and behavioural risk factors involved in the development of PF, providing a scientific basis for preventive measures and orthotic approaches. Assessment Parameters: Medical History Form 1. Demographic data: Age, height, weight, BMI 2. Foot anthropometric measurements 3. Footwear preference: Footwear Assessment Score ( Footwear Assessment Score ) 4. Lower extremity joint health: History of pain, injury, or limitation in the knee and hip joints 5. Daily step count: Measurement using the Step Counter mobile application 6. Physical activity level: IPAQ-SF (International Physical Activity Questionnaire - Short Form) questionnaire

Interventions

None listed

Sponsors

Medipol University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Being between 18 and 65 years of age, * Having been diagnosed with plantar fasciitis, * Having heel pain complaints originating from the plantar medial calcaneal tubercle, * Pain complaints being most pronounced in the first steps taken in the morning or after rest,

Exclusion criteria

* Any cardiopulmonary, dermatological, neurological or orthopaedic problems, * History of lower limb surgery, * Use of assistive devices (walker, crutches, etc.) * Cognitive, mental and/or psychological problems * Pregnancy * Lower limb amputation

Design outcomes

Primary

MeasureTime frameDescription
Anthropometric measurements of the footbaseline* Foot length * Metatarsal width * Medial arch height

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026