NCT06879756

Brief Summary

The purpose of this study was to determine the relationship between flexible flatfoot and lumbar proprioception.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
57

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 9, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2025

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 22, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 10, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 17, 2025

Completed
Last Updated

March 17, 2025

Status Verified

March 1, 2025

Enrollment Period

3 months

First QC Date

March 10, 2025

Last Update Submit

March 11, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • assessment of the foot posture using navicular drop test

    The study evaluates foot posture in a weight-bearing position by placing the thumb and index fingers on the medial and lateral aspects of the talar dome. The subject is then asked to invert and evert the hind-foot and ankle until equal depressions are felt. The distance between the navicular tubercle and the floor is measured. The navicular-drop score is recorded, and the subject is classified into a pronated foot (more than 10 mm of navicular drop) and a normal foot (between five and nine mm of navicular drop).

    at baseline

Secondary Outcomes (1)

  • assessment of change of lumbar proprioception using Biodex system isokinetic dynamometer

    at baseline

Study Arms (2)

flexible flat feet

28 patients suffering from flexible flatfoot were included in this group

normal subjects

27 normal subjects were included in this group

Eligibility Criteria

Age17 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

• Subjects with flexible flat foot posture according to the Navicular Drop Test by Brody method: a normal foot (between five and nine mm of navicular drop), apronated foot (more than 10 mm of navicular drop).

You may qualify if:

  • subjects of both sexes (females and males) were selected and assigned into two groups
  • Patient's age range was between 17 to 30 years old.
  • Subjects with flexible flat foot posture according to the Navicular Drop Test by Brody method: a normal foot (between five and nine mm of navicular drop), pronated foot (more than 10 mm of navicular drop).
  • Patients will be willing and able to participate in assessment without cognitive impairments that would limit their participation

You may not qualify if:

  • The potential participation was excluded when they had one of the following criteria:
  • Repeated lower extremity injuries, such as fractures or deformities.
  • History of surgery to the lower extremity.
  • history of back surgery
  • rheumatologic disorders
  • spine infections
  • ankle fracture
  • lumbar fracture
  • spondylosis
  • lumbar disc bulge
  • spondylolisthesis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

out-patient clinic, faculty of physical therapy, Cairo university

Cairo, Egypt

Location

MeSH Terms

Conditions

FlatfootSpinal InjuriesSomatosensory Disorders

Condition Hierarchy (Ancestors)

TalipesFoot Deformities, AcquiredFoot DeformitiesMusculoskeletal DiseasesFoot Deformities, CongenitalLower Extremity Deformities, CongenitalLimb Deformities, CongenitalMusculoskeletal AbnormalitiesCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesBack InjuriesWounds and InjuriesSensation DisordersNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

March 10, 2025

First Posted

March 17, 2025

Study Start

October 9, 2024

Primary Completion

January 15, 2025

Study Completion

January 22, 2025

Last Updated

March 17, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Locations