- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04249765
Hand Strength And Hand-Reaction Parameters Of Post Millennial: An Example Of Students' Group In Central Anatolia (HS)
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Middle Anatolia
-
Ankara, Middle Anatolia, Turkey, 06520
- Recruiting
- Atılım University
-
Contact:
- Mehmet Turan, Doç.Dr.
- Phone Number: +90 (312) 586 80 00
- Email: sofia.ostrovska@atilim.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy volunteers
Exclusion Criteria:
- History of any upper extremity pain or injury
Study Plan
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
Collaborators
Investigators
- Study Director: Mehmet Turan, Doç. Dr., Atılım University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ANTICIPATED)
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
Keywords
Other Study ID Numbers
- 12068451748
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
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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