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CompletedNCT07083921handloadUpdated Jul 24, 2025

Effect of Load Carry on Dynamic Plantar Pressure

An interventional study of plantar pressure in Plantar Pressure Distrubution, sponsored by Medipol University. Completed at 2 sites in Turkey (Türkiye). Open to participants aged 20 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-24.

Sponsored by Medipol University · Not applicable, Interventional, and Screening

From the registry’s dates

  • Registered 4 years 4 months after the study started (first participant enrolled Jan 2021, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
20 Years to 55 Years
Sex
All
01

Study summary

The aim of the study was to investigate the effect of loads carried with the dominant and non-dominant hand on dynamic plantar pressure parameters in healthy individuals.Participants were required to be between the ages of 20 and 55 years, and to be free from systemic, neurological, orthopaedic or chronic diseases. Individuals with physical or mental disabilities, balance problems, a risk of falling, knee or wrist-hand joint instability, or who were pregnant, were excluded from the study.

H1:Carrying load on the dominant hand increases dynamic plantar pressure parameter values.

H0: Carrying load in the dominant hand does not change the dynamic plantar pressure parameter values.

Read the detailed description

Background: Individuals carry loads with their right or left hand due to their daily life activities. The load carried causes biomechanical differences on the body.

Research Question: The aim of the study was to investigate the effect of loads carried with the dominant and non-dominant hand on dynamic plantar pressure parameters in healthy individuals.

Method: 20 healthy participants aged 20-55 years participated in the study voluntarily. The participants were asked to walk at least six laps at normal walking speed while carrying a load weighing 4 kg with their right and then their left hands. The Sensor Medica pedobarography device was used to evaluate dynamic plantar pressure.

02

Conditions studied

  • Plantar Pressure Distrubution

Keywords

  • Dominant Hand
  • Non-Dominant Hand
  • load
  • dynamic plantar pressure
03

In context

Lead sponsor

Medipol University is the lead sponsor of 311 studies on the registry; 86 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • between the ages of 20-55
  • without any systemic, neurological, orthopaedic and chronic diseases

Exclusion criteria

Exclusion Criteria:

  • pregnant,
  • physical and mental problems
  • having balance problems and high risk of falling
  • with joint instability
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Dominant hand

    Participants are evaluated only once.

    Device: plantar pressure

Interventions

  • Deviceplantar pressure

    Healthy individuals carry loads with their dominant and non-dominant hands.

    Also known as: gait analysis

06

What researchers measure

Primary outcomes

  1. Plantar Pressure

    Plantar pressure will be measured with a baropodometer. The maximum pressure occurring at the time of measurement during load bearing shall be evaluated.

    Time frame: Baseline

07

Study locations

2 sites
  • Istanbul Medipol University
    Beykoz, Istanbul 34290, Turkey (Türkiye)
  • Istanbul Medipol University
    Istanbul, Istanbul 34290, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07083921
Lead sponsor
Medipol University
Responsible party
Hande YAZICI (Lecturer, Medipol University) — Principal investigator
First posted
Jul 24, 2025
Start date
Jan 15, 2021
Primary completion
Oct 15, 2021
Completion
Oct 15, 2021
Last update
Jul 24, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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