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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03557866
Other study ID # 380/17
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 22, 2018
Est. completion date November 1, 2018

Study information

Verified date November 2018
Source University of Haifa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

Individual with and without pronated foot will be recruited. Pronation will be defined according to navicular drop test. Inclusion criteria : individual who run on a regular basis at least 3 times per week for one hour, can run 5 Km in less then 40 minutes, without past injuries during the last year of Achilles tendon or other lower extremities pain.

Individuals will be asked to run for 5 Km in self selected velocity. The Milestone pod device will be used to monitor kinematic parameters.

functional test will be conducted before and after the running as follows: heel raise test and one leg hop for distance test.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date November 1, 2018
Est. primary completion date November 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- 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

Exclusion Criteria:

- previous surgery in lower extremities

- Achilles tendon pain during the last year

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
running
individuals will be asked to run for 5 km in self selected speed

Locations

Country Name City State
Israel University of Haifa Haifa

Sponsors (1)

Lead Sponsor Collaborator
University of Haifa

Country where clinical trial is conducted

Israel, 

References & 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. — View Citation

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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary stride length stride length in cm up to 6 months
Primary cadence steps per minute up to 6 months
Secondary velocity running velocity in Km/hour up to 6 months
Secondary heel raise test how many good heel raise till fatigue up to 6 months
See also
  Status Clinical Trial Phase
Completed NCT05347186 - Effects of 8-weeks Systematic Corrective Exercise Program in Pronation Distortion Syndrome N/A