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Completed

NCT Number: NCT06937879

Investigation of Factors Affecting Upper Extremity Function in Healthy Young Adults

The aim of this study was to determine the effects of grip strength, motor imagery and two-point discrimination on upper extremity function in healthy young adults.

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Observational

Primary location

KTO Karatay University

Karatay, Konya, 42020, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being a university student,
  • Being between the ages of 18-35
  • Not having any known upper extremity problems

Exclusion criteria

  • Upper extremity surgery history
  • Neurological problems
  • Chronic diseases

Treatment and study plan

Hand grip strength

Other

The grip strength of the participants will be performed with a hydraulic hand dynamometer on a chair with back and arm support. The participant will be asked to squeeze the dynamometer with maximum force. The measurement will be performed 3 times and the average value will be recorded.

Primary outcomes

  1. Function

    Time frame: Baseline

    The Turkish version of the Shoulder, Arm and Hand Problems Questionnaire (DASH-T) will be used to assess the functional level of the upper extremity [10]. The DASH-T questionnaire consists of 30 questions. The first 20 questions ask about physical ability and the last 10 questions ask about pain and related functional and environmental limitations. As the score approaches zero, the functional level of the person is high; as the score moves away from zero, the functional level of the person is low.

Secondary outcomes

  1. Grip strength

    Time frame: Baseline

    The grip strength of the participants will be performed with a hydraulic hand dynamometer on a chair with back and arm support. The participant will be asked to squeeze the dynamometer with maximum force. The measurement will be performed 3 times and the average value will be recorded.

  2. Motor imagery

    Time frame: Baseline

    Motor imagery will be assessed through a left/right judgment task in which participants will be required to recognize whether hand images correspond to their left or right side using the Recognise™ application (Neuro Orthopaedic Institute, Adelaide, Australia). For this test, participants will be seated comfortably in front of a table, with both elbows flexed at 90◦ and both index fingers placed at the bottom of the screen of an electronic tablet. Multiple images of forearms (20 on each side) in multiple postures, angles and skin colors will be randomly displayed in the center of the screen of the device. Participants will be given standard instructions to decide as quickly and accurately as possible whether each image is of the right or left hand by clicking on the 'left' (left fingers) or 'right' (right fingers) buttons displayed at the bottom of the screen.

  3. Two-point discrimination

    Time frame: Baseline

    Two-point discrimination will be assessed using a two-dot discriminator placed longitudinally and perpendicular to the index fingertip. The test score is the minimum distance at which the participant can discriminate between two dots in five consecutive trials. The assessment starts with a distance of 4 mm and is gradually reduced or increased depending on the participant's performance. A distance greater than 4 mm is considered impaired

Sponsors and collaborators

Lead sponsor

KTO Karatay University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 22, 2025
Registry last updated
May 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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