NCT03557866

Brief Summary

The aim of the study is to examine the kinematic parameters of individuals with pronated foot compared with individuals with normal foot

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2018

Shorter than P25 for not_applicable

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

First Submitted

Initial submission to the registry

June 4, 2018

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 15, 2018

Completed
7 days until next milestone

Study Start

First participant enrolled

June 22, 2018

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2018

Completed
Last Updated

November 27, 2018

Status Verified

November 1, 2018

Enrollment Period

4 months

First QC Date

June 4, 2018

Last Update Submit

November 26, 2018

Conditions

Keywords

foot posturerunningfoot index

Outcome Measures

Primary Outcomes (2)

  • stride length

    stride length in cm

    up to 6 months

  • cadence

    steps per minute

    up to 6 months

Secondary Outcomes (2)

  • velocity

    up to 6 months

  • heel raise test

    up to 6 months

Study Arms (2)

pronated group

EXPERIMENTAL

individuals with pronated foot

Diagnostic Test: running

control group

ACTIVE COMPARATOR

individuals with normal foot posture

Diagnostic Test: running

Interventions

runningDIAGNOSTIC_TEST

individuals will be asked to run for 5 km in self selected speed

Also known as: kinematic parameters of running
control grouppronated group

Eligibility Criteria

Age20 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • running on a daily basis at least 3 times per week with minimum of 1 hour
  • capable to run 5 km in less then 40 minutes
  • willing to participate in the study

You may not qualify if:

  • previous surgery in lower extremities
  • Achilles tendon pain during the last year

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Haifa

Haifa, Israel

Location

Related Publications (2)

  • McPoil TG, Cornwall MW, Medoff L, Vicenzino B, Fosberg KK, Hilz D. Arch height change during sit-to-stand: an alternative for the navicular drop test. J Foot Ankle Res. 2009 May 18;2:17. doi: 10.1186/1757-1146-2-17.

  • Murley GS, Menz HB, Landorf KB. Foot posture influences the electromyographic activity of selected lower limb muscles during gait. J Foot Ankle Res. 2009 Nov 26;2:35. doi: 10.1186/1757-1146-2-35.

MeSH Terms

Interventions

Running

Intervention Hierarchy (Ancestors)

LocomotionMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaExerciseMotor Activity

Study Officials

  • Gali Dar, PHd

    University of Haifa

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SCREENING
Intervention Model
PARALLEL
Model Details: two groups. Individuals with and without pronated foot.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

June 4, 2018

First Posted

June 15, 2018

Study Start

June 22, 2018

Primary Completion

November 1, 2018

Study Completion

November 1, 2018

Last Updated

November 27, 2018

Record last verified: 2018-11

Data Sharing

IPD Sharing
Will share

the results of the study will be analysed. a paper will be submitted to international journal with study description including methods, examination protocol and results

Shared Documents
STUDY PROTOCOL, CSR
Time Frame
following completion of data collection
Access Criteria
according to journal policy

Locations