Comparison Of Effects Virtual Reality and Short Foot Exercises On Balance and Performance in Pes Planus

July 28, 2020 updated by: Tezel Yıldırım Şahan, Hacettepe University

Effect of Virtual Reality on Pes Planus

Virtual reality exercises have become increasingly popular in recent years. After the increase in usage areas in daily life, its use in healthcare has become widespread. Flatfoot is one of the orthopedic problems with high prevalence, especially in young individuals. In the literature, conservative treatment methods of flat soles are mentioned as exercise, shoe modifications, and orthotic methods. In the study, it is planned to investigate whether individuals with flat-footed virtual reality exercises contribute to conservative treatment.

The aim of this study was to investigate the effect of virtual reality exercises on individuals with pes planus.

Study Overview

Status

Completed

Conditions

Detailed Description

To show whether virtual reality exercises will contribute to decrease of flat footing, improvement of balance and increase of performance of individuals with flat foot.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Yahşihan
      • Kırıkkale, Yahşihan, Turkey, 71140
        • Kırıkkale University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Have pes planus,
  • Volunteer for this study,
  • Climb 10 stairs independently,
  • Can stand one single leg

Exclusion Criteria:

  • History of trauma, fracture or operation of the foot, knee, and hip that will affect the foot
  • Having visual, hearing and mental problems that prevent participation in virtual reality exercises,
  • Being diagnosed with orthopedic or neurological problems that prevent standing on a single leg

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Exercise Group
One group only treated with short foot exercises.
Short Foot Exercises
Active Comparator: Virtual Reality Group
The second group treated with virtual reality
Exercise with virtual reality

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
comparison of exercise and virtual reality treatment on balance
Time Frame: 15 minute
Y balance test measure with second (sn)
15 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of exercise on performance
Time Frame: 10 minute
10 step test measure with minute
10 minute
Navicular Drop Test
Time Frame: 5 minute
Measure of navicular tubercul from floor measure with santimeter(cm)
5 minute
Femoral anteversion test
Time Frame: 5 minute
measure of hip internal rotation movement actively measure with universal goniometer (degree)
5 minute

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Study Director: Cevher Demirci, Dr, Kırıkkale University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 5, 2019

Primary Completion (Actual)

March 10, 2020

Study Completion (Actual)

March 20, 2020

Study Registration Dates

First Submitted

July 5, 2019

First Submitted That Met QC Criteria

February 21, 2020

First Posted (Actual)

February 25, 2020

Study Record Updates

Last Update Posted (Actual)

July 30, 2020

Last Update Submitted That Met QC Criteria

July 28, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The subjects were randomly assigned to one of the groups using an online random allocation software program. All groups were taken into a 4-week treatment program. At the end of the treatment process, it was given to subjects including VR and SF program aiming foot muscles.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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