Hand Strength And Hand-Reaction Parameters Of Post Millennial: An Example Of Students' Group In Central Anatolia (HS)

January 26, 2021 updated by: İSMAİL CEYLAN, Ahi Evran University Education and Research Hospital
The aim of this research is to find out whether there exists a correlation between such important characteristic of individual's hand performance as grip strength, pinch strength, and the hand reaction. In addition, it will be investigated whether there is a change in normative values of this age group in relation to modern lifestyle. The study includes statistical data analysis and interpretation of the derived outcomes.

Study Overview

Status

Unknown

Conditions

Detailed Description

Objective: To investigate correlation between grip force, pinch strength and hand reaction in a group of post-millennial in Central Anatolia, and also to provide a comparison to previously available results on millennial.

Methods: Experimental data were collected by healthy subjects, who are university students. The sample comprises females and males, consented to participate in the study. The ages of the subjects will range from 18 to 25 years. Grip strength will measure with hand dynamometer and pinch strength will measure with pinch meter. Hand reaction will test with the Ruler Drop Test.

For each subject, body mass, height and hand preference will be record. The study will be completed in accordance with the norms of the Declaration of Helsinki and was approved by the ethics committee of the University of Atilim (Turkey).

The collected data will be undergone statistical analysis to extract any feasible conclusions. First, the correlation coefficients will be found to determine whether there is a noticable relationship between the independent variables grip strength and pinch strength versus the dependent variable ruler drop test. The calculated sample correlation coefficients have been tested for the significance.

Study Type

Interventional

Enrollment (Anticipated)

110

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

    • Middle Anatolia
      • Ankara, Middle Anatolia, Turkey, 06520

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:

  • Healthy volunteers

Exclusion Criteria:

  • History of any upper extremity pain or injury

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: SCREENING
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Hand strength

Grip Strength The participants sat upright on a chair with their feet supported. The tested arm was positioned on a table with the shoulders slightly abducted and neutrally rotated, the elbow in 90° of flexion, the forearm in 0° between pronation and supination, and the wrist in neutral resting position. The participants were instructed to maintain that position during the test. The grip strength of both hands was measured using the Hand Dynamometer

3. Pinch Strength Participants were seated at a table on which the dynamometers were positioned.

The subjects were told to keep their elbow flexed without resting their arm or the grip handle of the dynamometer.

Grip Strength The participants sat upright on a chair with their feet supported. The tested arm was positioned on a table with the shoulders slightly abducted and neutrally rotated, the elbow in 90° of flexion, the forearm in 0° between pronation and supination, and the wrist in neutral resting position. The participants were instructed to maintain that position during the test. The grip strength of both hands was measured using the Hand Dynamometer.

3. Pinch Strength Participants were seated at a table on which the dynamometers were positioned. The subjects were told to keep their elbow flexed without resting their arm or the grip handle of the dynamometer on the table.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hand grip strength
Time Frame: Measurements will assessed in 1 month and data will analysed in 2 months.
The participants will sit upright on a chair with their feet supported. The tested arm will positioned on a table with the shoulders slightly abducted and neutrally rotated, the elbow in 90° of flexion, the forearm in 0° between pronation and supination, and the wrist in neutral resting position. The grip strength of both hands will measured using the Hand Dynamometer. Results will be evaluated in kilograms.
Measurements will assessed in 1 month and data will analysed in 2 months.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hand Pinch Strength
Time Frame: Measurements will assessed in 1 month and data will analysed in 2 months.
Participants were seated at a table on which the dynamometers were positioned. The subjects were told to keep their elbow flexed without resting their arm or the grip handle of the dynamometer on the table. Results will be evaluated in kilograms.
Measurements will assessed in 1 month and data will analysed in 2 months.
Ruler Drop Test
Time Frame: Measurements will assessed in 1 month and data will analysed in 2 months.
During the test, the students had to sit having the upper arm forming an angle of 90 degrees with the mid forearm, which lies on a flat horizontal table surface. The hand is required to be open and positioned at the edge of the surface. Results will be evaluated in cm.
Measurements will assessed in 1 month and data will analysed in 2 months.

Collaborators and Investigators

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

Collaborators

Investigators

  • Study Director: Mehmet Turan, Doç. Dr., Atılım 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)

January 1, 2020

Primary Completion (ACTUAL)

February 25, 2020

Study Completion (ANTICIPATED)

March 25, 2021

Study Registration Dates

First Submitted

January 26, 2020

First Submitted That Met QC Criteria

January 29, 2020

First Posted (ACTUAL)

January 31, 2020

Study Record Updates

Last Update Posted (ACTUAL)

January 27, 2021

Last Update Submitted That Met QC Criteria

January 26, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 12068451748

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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