Smartphone & Headphone Effects on Baropodometric Parameters

October 23, 2024 updated by: HATİCE ÇETİN, Hacettepe University

Effects of Smartphone and Headphone Usage on Baropodometric Parameters in Healthy Individuals

The goal of this observational study is to observe baropodometric parameters such as postural sway and foot pressure distrubiton in healthy young participants between the ages of 18-35. The main questions it aims to answer are:

  • How does headphone usage affect baropodometric parameters in healthy young individuals?
  • How does texting affect baropodometric parameters in healthy young individuals?
  • How does headphone usage while texting affect baropodometric parameters in healthy young individuals?

Participants will:

  • Only be evaluated once.
  • Stand on the Baropodometric device platform while standing, texting, listening to music, texting while listening to music for the static and posturographic balance evaluation.
  • Walk on the baropdometric device platform while standing, texting, listening to music, texting while listening to music for dynamic evaluation.

Study Overview

Detailed Description

During our daily lives, the individuals perform many functions simultaneously. Two devices that modern technology has brought us are headphones and mobile phones, both of which are commonly used. Studies have shown that posture oscillation changes during walking while using a phone, but same studies also stated that more comprehensive studies are needed. There is no study in the literature that examines postural oscillation and foot pressure distribution while listening to music with headphones and messaging. The aim of this observational study is to evaluate the postural oscillation and foot pressure distribution during headphone use and messaging in healthy participants aged 18-35. The sample size of 35 participants was determined based on a similar study example using G-Power analysis. Participants will be assesed at Hacettepe University, Faculty of Physical Therapy and Rehabilitation. Participants will be selected based on eligibility criteria, and there will be only one group in the study; therefore, randomization will not be performed. Participants enrolled in the study will be evaluated using the FreeMED force platform (Sensor Medica, Italy). The platform itself is 40x40 cm in size and comes with two plates, each one meter long. When all components are assembled, a continuous surface of 2.4 meters is obtained. Participants will participate in static, posturographic, and dynamic evaluations. In each evaluation, participants will first stand still, then put on headphones and listen to music at 80 decibels with a tempo of 130 bpm, then type a message, and finally type a message while listening to music. Static evaluation will provide information about foot pressure distribution; posturographic evaluation will include Romberg tests with eyes open, eyes closed, standing on one foot, and standing on two feet; and dynamic evaluation will assess participants' walking phases and speed. The statistical analysis of the study will be performed using SPSS 23.0 software.

Study Type

Observational

Enrollment (Actual)

35

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

      • Ankara, Turkey
        • Hacettepe University
      • Ankara, Turkey, 06800
        • Hatice Cetin

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Healthy young people who are volunteering to participate the study.

Description

Inclusion Criteria:

  • Agreeing to participate in the study voluntarily,
  • Being between the ages of 18-35

Exclusion Criteria:

  • Not agreeing to participate in the study voluntarily.
  • Having a congenital spinal cord anomaly
  • Existing neurological, orthopedic, inflammatory, cardiovascular, rheumatological, vestibular problems
  • Having a surgical history of the spinal region

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Headphone and Smartphone Usage Group
The group where participants listen to music while messaging and also where these activities are evaluated separately. The only group in the study.
Asessment of participants' static balance and pressure distrubiton, posturographic balance and dynamic balance whilst using headphones and messaging.
Other Names:
  • FreeMed Baropodometric Device

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Baropodometer assessments- Static pressure distribution
Time Frame: through study intervention, an average of 15 minutes
Pressure distribution will be assessed with FreeMed baropodometric platform and the recording measurement unit will be percentages.
through study intervention, an average of 15 minutes
Baropodometer assessments- Posturographic center of gravity
Time Frame: through study intervention, an average of 15 minutes
Center of gravity will be assessed with FreeMed baropodometric platform and the recording measurement unit will be milimeters.
through study intervention, an average of 15 minutes
Baropodometer assessments- Posturographic oscillations
Time Frame: through study intervention, an average of 15 minutes
Oscillations will be assessed with FreeMed baropodometric platform and the recording measurement unit will be milimeters.
through study intervention, an average of 15 minutes
Baropodometer assesments - Posturographic Sway Length
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and the recording measurement unit will be milimeters.
through study intervention, an average of 15 minutes
Baropodometer assesments - Posturographic Displacement Towards X and Y axis
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and the recording measurement unit will be milimeters.
through study intervention, an average of 15 minutes
Baropodometer assessments- Posturographic average sway velocity
Time Frame: through study intervention, an average of 15 minutes
Sway velocity will be assessed with FreeMed baropodometric platform and the recording measurement unit will be degrees.
through study intervention, an average of 15 minutes
Baropodometer assessments- Dynamic average surface
Time Frame: through study intervention, an average of 15 minutes
Average surface will be assessed with FreeMed baropodometric platform and the recording measurement unit will be cm.
through study intervention, an average of 15 minutes
Baropodometer assessments- Dynamic average speed
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and the recording measurement unit will be milimeters/second.
through study intervention, an average of 15 minutes
Baropodometer assesments - Dynamic Gait Phase Durations
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and the recording measurement unit will be percentages
through study intervention, an average of 15 minutes
Feet Loading Pattern - Dynamic Longitudinal Arc
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and will be used to asses the feet loading pattern.
through study intervention, an average of 15 minutes
Feet Loading Pattern - Forefoot Reatfoot Load
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and will be used to asses the feet loading pattern.
through study intervention, an average of 15 minutes
Feet Loading Pattern - Medial Lateral Load
Time Frame: through study intervention, an average of 15 minutes
It will be assessed with FreeMed baropodometric platform and will be used to asses the feet loading pattern.
through study intervention, an average of 15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Cognitive Flexibility Inventory
Time Frame: At Baseline
The Cognitive Flexibility Inventory is a 20-item self-report measure to monitor how often individuals engaged in cognitive behavioural thought challenging interventions. The total score ranges between 20 and 140, where higher scores indicate more cognitive flexibility.
At Baseline
Forward Head Posture
Time Frame: At Baseline
It will be assessed with a digital inclinometer, the measurement unit will be in degrees.
At Baseline
New York Posture Assesment
Time Frame: At Baseline
This form will assess participants' postural alignment. Total scores range from 13 to 65, with results categorized as: 'excellent' (above 45), 'good' (40-44), 'fair' (30-39), 'poor' (20-29), and 'very poor'.
At Baseline
International Physical Activity Questionnaire
Time Frame: At Baseline
This form will assess participants' physical fitness and well-being. Based on MET minutes per week, the results are categorized into three activity levels: inactive, minimally active and very active.
At Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hatice Cetin, Hacettepe University

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)

April 25, 2024

Primary Completion (Actual)

July 28, 2024

Study Completion (Actual)

October 23, 2024

Study Registration Dates

First Submitted

April 29, 2024

First Submitted That Met QC Criteria

May 2, 2024

First Posted (Actual)

May 6, 2024

Study Record Updates

Last Update Posted (Actual)

October 24, 2024

Last Update Submitted That Met QC Criteria

October 23, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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