Investigation of Functional Parameters

September 17, 2024 updated by: Barış SEVEN, Gazi University

Investigation of Functional Parameters: Relationships Between Bimanual Coordination, Proprioception, Manuel Dexterity, and Strength

The goal of this cross-sectional study is to investigate the relationships between grip/pinch strengths, wrist flexion-extension strengths, wrist proprioception, manual dexterity, and bimanual coordination in healthy volunteers. The hypotheses are:

H0: There is no relationship between grip/pinch strengths, wrist flexion-extension strengths, wrist proprioception, manual dexterity, and bimanual coordination.

H1: There is a relationship between grip/pinch strengths, wrist flexion-extension strengths, wrist proprioception, manual dexterity, and bimanual coordination.

Within the scope of the study, the participants' active joint position sense (AJPS) and flexion-extension strengths of the wrist were assessed using an isokinetic dynamometer. Additionally, grip strength, key pinch, tip pinch, and palmar pinch strengths were evaluated using a dynamometer. The Purdue Pegboard Test was used to assess manual dexterity and bimanual coordination.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

25

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

    • Çiğli
      • İzmir, Çiğli, Turkey
        • Barış SEVEN

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

No specific age or disease/injury group is targeted. The study was conducted with healthy volunteers.

Description

Inclusion Criteria:

After providing detailed information about the research, individuals who agreed to participate were included in the study.

Exclusion Criteria:

Individuals who had undergone surgery or trauma in the upper extremity, had fractures or acute orthopedic injuries, had a history of neuromuscular diseases or congenital anomalies, had skin infections, or other conditions that could affect the assessment within the past 6 months were excluded from 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Purdue Pegboard Test was used to assess bimanual coordination.
Time Frame: Participants will be evaluated only once.
In the Purdue Pegboard test, participants, seated in front of the test board, were asked to placed pins into the holes on both sides of the board simultaneously with both hands as many pins as possible within 30 seconds. The total number of pins placed was recorded as the score for bimanual coordination.
Participants will be evaluated only once.
The Purdue Pegboard Test was used to assess manual dexterity.
Time Frame: Participants will be evaluated only once.
In the Purdue Pegboard test, participants, seated in front of the test board, were first asked to use their dominant hand to pick up pins from the dominant side and place them into the holes on the same side, from top to bottom. They were instructed to place as many pins as possible within 30 seconds. The number of pins placed was recorded as the score for dominant hand manual dexterity. The same test was then conducted for the nondominant side.
Participants will be evaluated only once.
The active joint position sense was assessed using an isokinetic dynamometer.
Time Frame: Participants will be evaluated only once.

For the assessment of wrist proprioception, an isokinetic dynamometer with demonstrated reliability [Cybex NORM®, Humac, CA, USA] was used.

Wrist proprioception was assessed by Active Joint Position Sense (AJPS) measurement. During the test, participants wore eye masks. For the AJPS assessment, the target angle was set at 30° extension, which is the functional position of the wrist. Participants were asked to actively move their wrist from the neutral position to the 30° extension and hold this position for 5 seconds. This trial was repeated three times. Participants were then asked to find the target angle three times. The amount of error between the target angle and the achieved angle was used to define the accuracy of the active joint position sense. The arithmetic mean of these three measurements was calculated and recorded.

Participants will be evaluated only once.
The flexion-extension strengths of the wrist were assessed using an isokinetic dynamometer.
Time Frame: Participants will be evaluated only once.

Wrist flexion and extension strengths were also evaluated using the Cybex isokinetic dynamometer. These strength assessments were conducted in the same position and range of motion as the proprioception evaluations. Before starting the measurements, participants were informed about the test. At the beginning of the test, three practice trials were performed. The concentric-concentric strength measurement was conducted with an angular velocity of 60°/s for 5 repetitions. A 20-second rest period was allowed between the practice and test trials. The peak torque parameters for wrist flexion and extension in both wrists were measured.

Assessments began with the dominant side. Subsequently, the same measurements were repeated on the other extremity by adjusting the position of the dynamometer and chair. The device was calibrated before the participants were evaluated. All measurements were conducted by the same person to prevent inter-rater variability.

Participants will be evaluated only once.
Grip and pinch strengths were measured using a digital dynamometer.
Time Frame: Participants will be evaluated only once.
The assessment of gross grip strength was performed using a digital dynamometer (J-Tech Commender Grip Track). Measurements were taken with the participant seated, the elbow flexed at 90 degrees, the wrist in up to 30 degrees of extension, and the forearm in a neutral rotation position. The dynamometer's grip width was set to the second level. Maximum grip force was measured by having the participant squeeze as hard as possible three times, and the arithmetic mean of these three measurements was calculated. Key pinch, palmar pinch, and tip pinch strength measurements were conducted using a pinch gauge (Baseline Mechanical Pinch Gauge, 60 lb) in the same position and with the same measurement technique as the gross grip strength assessment. All evaluation protocols were established according to the recommendations of the American Society of Hand Therapists.
Participants will be evaluated only once.

Collaborators and Investigators

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

April 12, 2023

Primary Completion (Actual)

January 12, 2024

Study Completion (Actual)

January 12, 2024

Study Registration Dates

First Submitted

September 17, 2024

First Submitted That Met QC Criteria

September 17, 2024

First Posted (Estimated)

September 19, 2024

Study Record Updates

Last Update Posted (Estimated)

September 19, 2024

Last Update Submitted That Met QC Criteria

September 17, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 4

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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