The Reliability of Myotonometer in Evaluating the Muscle Tone and Biomechanical Properties of the Forearm Muscles

Sponsor
İlke KARA, PT (Other)
Overall Status
Completed
CT.gov ID
NCT05183659
Collaborator
Bitlis Eren University (Other), Dokuz Eylul University (Other)
56
1
1.3
43.7

Study Details

Study Description

Brief Summary

The primary aim of this study was to evaluate the intra-rater and inter-rater reliability of MyotonPRO in measuring muscle tone and mechanical properties of the wrist extensor and flexor muscles in healthy young adults. The secondary aim is to examine whether grip strength has any effect on muscle tone and biomechanical properties.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    56 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    The Reliability of Myotonometer in Evaluating the Muscle Tone and Biomechanical Properties of the Forearm Muscles: Investigation of the Effect of Grip Strength on Mechanical Features
    Actual Study Start Date :
    Nov 27, 2021
    Actual Primary Completion Date :
    Dec 29, 2021
    Actual Study Completion Date :
    Jan 5, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Muscle tone (Hz) [Day 1]

      The muscle tone which is a biomechanical property of the forearm muscles will be evaluated with a portable hand-held myotonometer. This myotonometer (MyotonPRO - Tallinn, Estonia) is non-invasive and provides a quantitative assessment of a muscle's biomechanical properties. The MyotonPRO applies a short-intensity mechanical impulse on the skin overlying the muscle or facia. The tissue's response then generates a signal that is recorded, and an internal software program produces an acceleration graph. To determine the feasibility of the MyotonPRO for assessing the muscle tone of forearm muscles measurements will be performed and recorded.

    2. Stiffness (N/m) [Day 1]

      The stiffness which is a biomechanical property of the forearm muscles will be evaluated with a portable hand-held myotonometer. This myotonometer (MyotonPRO - Tallinn, Estonia) is non-invasive and provides a quantitative assessment of a muscle's biomechanical properties. The MyotonPRO applies a short-intensity mechanical impulse on the skin overlying the muscle or facia. The tissue's response then generates a signal that is recorded, and an internal software program produces an acceleration graph. To determine the feasibility of the MyotonPRO for assessing the stiffness of forearm muscles measurements will be performed and recorded.

    3. Elasticity (Logarithmic decrement) [Day 1]

      The elasticity which is a viscoelastic property of the forearm muscles will be evaluated with a portable hand-held myotonometer. This myotonometer (MyotonPRO - Tallinn, Estonia) is non-invasive and provides a quantitative assessment of a muscle's viscoelastic properties. The MyotonPRO applies a short-intensity mechanical impulse on the skin overlying the muscle or facia. The tissue's response then generates a signal that is recorded, and an internal software program produces an acceleration graph. To determine the feasibility of the MyotonPRO for assessing the stiffness of forearm muscles measurements will be performed and recorded.

    Secondary Outcome Measures

    1. Grip Strength [Day 1]

      Handgrip strength will be measured with the JAMAR Hydraulic Hand Dynamometer. Participants will be asked to sit down with knees and hip flexed to 90⁰, forearm in a neutral position, wrist in 0-30⁰ extension, and 0-5⁰ ulnar deviation while on a chair with backrest. During the measurement, the examiner will instruct them to squeeze the handles of the dynamometer as strongly as possible and then let them loose completely, with a loud motivating command. This will be repeated 3 times with 1-minute rest breaks and the average value will be calculated. During the measurements, the Jamar dynamometer will be grasped from the lower and upper parts by the examiner.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age≥18 years

    • Body mass index < 30 kg/meter square

    • Having no upper extremity injuries

    • Willing and able to provide the written informed consent for the study

    Exclusion Criteria:
    • Use of medication that will affect muscle tone

    • History of lateral or medial epicondylitis, trauma (elbow, hand or wrist), cervical radiculopathy, peripheral neuropathy or nerve injury (axillary, median, ulnar, radial, musculocutaneous), systemical diseases, muscle disorders (e.g. genetic diseases, neuromuscular disorders)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bitlis Eren University Bitlis Turkey 13000

    Sponsors and Collaborators

    • İlke KARA, PT
    • Bitlis Eren University
    • Dokuz Eylul University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    İlke KARA, PT, Co-Principal Investigator, Dokuz Eylul University
    ClinicalTrials.gov Identifier:
    NCT05183659
    Other Study ID Numbers:
    • BEU-IK-01
    First Posted:
    Jan 10, 2022
    Last Update Posted:
    Jan 10, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by İlke KARA, PT, Co-Principal Investigator, Dokuz Eylul University

    Study Results

    No Results Posted as of Jan 10, 2022