- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07083921
- Original Trial
Effect of Load Carry on Dynamic Plantar Pressure (handload)
Effect of Dominant and Non-dominant Hand Load Carry on Dynamic Plantar Pressure
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.
Study Overview
Status
Conditions
Intervention / Treatment
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Istanbul, Turkey, 34290
- Istanbul Medipol University
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İstanbul
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Beykoz, İstanbul, Turkey, 34290
- Istanbul Medipol University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- between the ages of 20-55
- without any systemic, neurological, orthopaedic and chronic diseases
Exclusion Criteria:
- pregnant,
- physical and mental problems
- having balance problems and high risk of falling
- with joint instability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dominant hand
Participants are evaluated only once.
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Healthy individuals carry loads with their dominant and non-dominant hands.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plantar Pressure
Time Frame: Baseline
|
Plantar pressure will be measured with a baropodometer.
The maximum pressure occurring at the time of measurement during load bearing shall be evaluated.
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HIsci
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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