Dominant Non-Dominant Upper Extremity in Gender

March 9, 2024 updated by: METEHAN YANA, Karabuk University

Dominant and Non-Dominant Upper Extremity in Young Individuals

There are strength and functional differences between non-dominant and dominant extremities. This is important in the hand and extremity rehabilitation process. This situation also differs between genders. Comparison of the dominant and non-dominant limb can provide important clinical or rehabilitation field-related information. It is reported in the literature that manual dexterity, grip strength and joint position sense may differ between extremities. However, the relationship between this situation and the difference between genders has not been explained. It is thought that examining this difference can be extremely useful in determining achievable goals in hand rehabilitation and in customizing care for different groups.

Study Overview

Status

Recruiting

Detailed Description

Many treatment protocols compare the strength of the injured extremity to the uninjured extremity or compare it to normative data from the same group of individuals. There is controversy about the difference in grip strength between dominant and non-dominant hands in left- and right-hand dominant individuals. There is no study in the literature that evaluates the differences in muscle strength, joint position sense and upper extremity function skills between dominant and non-dominant upper extremities between genders. It is very important to include bilateral activity training in rehabilitation programs that aim to improve upper extremity mobility and speed. In addition, it will contribute to the accurate evaluation of activity and participation limitations, the determination of priorities, the selection of the right activity in task-specific and target-oriented treatment approaches, and the achievement of more effective results when integrated with technology-supported approaches. Therefore, the aim of our study is to fill this gap in the literature by comparing the differences between dominant and non-dominant upper extremities between genders.

Study Type

Observational

Enrollment (Estimated)

210

Contacts and Locations

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

Study Contact

Study Locations

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

Non-Probability Sample

Study Population

Healthy young adult individuals will be included in the study.

Description

Inclusion Criteria:

  1. Being between the ages of 18-25
  2. Volunteering to participate in the study

Exclusion Criteria:

  1. Having trauma (fracture, dislocation) in the last year
  2. Doing sports or activities that require bilateral activity (playing music, knitting, sports, etc.)
  3. Being diagnosed with any neurological or orthopedic disease that will affect hand-eye coordination
  4. Having had upper extremity surgery
  5. Having any Botox injection in the last 6 months
  6. Those who did not agree to participate in the study

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
Male
Hand preference was evaluated with the Edinburgh Hand Preference Questionnaire, grip muscle strength with the Jamar dynamometer, dexterity with the Purdue Pegboard Test, and proprioception as joint position sense with the inclinometer.
Female
Hand preference was evaluated with the Edinburgh Hand Preference Questionnaire, grip muscle strength with the Jamar dynamometer, dexterity with the Purdue Pegboard Test, and proprioception as joint position sense with the inclinometer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hand Preference
Time Frame: First Day
The Edinburgh Hand Preference Questionnaire questions individuals' hand use in daily living activities. The final total score is between 100 and -100. Individuals who score more than 40 points are right-hand; Individuals in this score range from 40 to -40 inclusive are recorded as ambidextrous, and individuals with scores of -40 points and below are left-handed
First Day
Grip Strength
Time Frame: First Day
Hand grip strength was measured using a standard Jamar Dynamometer.
First Day
Joint Position Sense
Time Frame: First Day
Proprioception was assessed by joint position sense (JPS) test. Shoulder JPS was assessed using a digital inclinometer
First Day
Manual Dexterity
Time Frame: First Day
The Purdue Pegboard Test was used to evaluate the functional skill levels of the upper extremities.
First Day

Collaborators and Investigators

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

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)

November 7, 2023

Primary Completion (Estimated)

March 15, 2024

Study Completion (Estimated)

March 30, 2024

Study Registration Dates

First Submitted

February 13, 2024

First Submitted That Met QC Criteria

February 13, 2024

First Posted (Actual)

February 21, 2024

Study Record Updates

Last Update Posted (Actual)

March 12, 2024

Last Update Submitted That Met QC Criteria

March 9, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Karabuk-001

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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