Anthropometric Parameters of the Foot and Plantar Fasciitis

NCT ID: NCT07151066

Last Updated: 2025-09-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-15

Study Completion Date

2025-12-30

Brief Summary

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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

Detailed Description

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Conditions

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Plantar Fasciitis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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PF Group

individuals with plantar fasciitis

No interventions assigned to this group

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medipol University

OTHER

Sponsor Role lead

Responsible Party

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Hande YAZICI

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Naile Hande İŞÇİ, PhD (c)

Role: STUDY_CHAIR

Medipol University

Locations

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Istanbul Medipol University

Istanbul, Beykoz, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E-10840098-202.3.02-5582

Identifier Type: -

Identifier Source: org_study_id

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