Reliability of Myotonometry in the Assessment of Mechanical Properties of Thenar Muscles

Sponsor
Ilke KARA (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06004635
Collaborator
(none)
40
1
14
2.9

Study Details

Study Description

Brief Summary

This study aims: (i) to determine the intra- and inter-observer reliability of myotonometry in assessing the mechanical properties of the thenar muscles [abductor pollicis brevis (APB) and flexor pollicis brevis (FPB)] in healthy subjects; (ii) to investigate the relationship between reaction time, left/right discrimination, grip strength and these mechanical properties.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Investigating the mechanical properties of hand muscles using simple applicable methods such as myotonometry can help to evaluate the effectiveness of programs used in hand rehabilitation, optimize the skills of performance-oriented individuals such as athletes and musicians, and create individualized treatment and training programs. In musculoskeletal-related pathologies such as carpal tunnel syndrome, studying the mechanical properties of the thenar muscles may be important to better understand hand grip strength, hand function and mobility. However, the use of myotonometer in the evaluation of the mechanical properties of the thenar muscles requires a reliability study. Accordingly, the aims of our study are: (i) to determine the intra- and inter-observer reliability of myotonometry in assessing the mechanical properties of the thenar muscles [abductor pollicis brevis (APB) and flexor pollicis brevis (FPB)] in healthy subjects; (ii) to investigate the relationship between reaction time, left/right discrimination, grip strength and these mechanical properties.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Reliability of Myotonometry in the Assessment of Mechanical Properties of Thenar Muscles: Relationship With Handgrip Strength, Reaction Time and Left/Right Discrimination
    Anticipated Study Start Date :
    Sep 1, 2023
    Anticipated Primary Completion Date :
    Sep 1, 2024
    Anticipated Study Completion Date :
    Nov 1, 2024

    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 and pinch strength [Day 1]

      Hand grip strength will be measured using a hydraulic hand dynamometer (Baseline). Pinch grip strength will be assessed using a hydraulic pinchmeter (Baseline). Standard procedures recommended by ASHT will be followed. Hand grip strength and pinch strength tests will be assessed with the elbow flexed 90 degrees as recommended by the American Society of Hand Therapists (ASHT).

    2. Reaction time [Day 1]

      BlazePod, a new technology for measuring individual reaction time (ms), will be used in the study. Participants will be asked to sit in a height-adjustable chair and position their dominant hand on the assessment table in as comfortable a position as possible. Once the participant's dominant hand is placed on the table, each pod will be placed 25 cm from the center of the hand to form a square pattern. Before starting the test, the participants will perform two practice trials in the same test setup as the real test in order to adapt to the test. Prior to the test, the mobile app will give the participant a three-second audible countdown warning and a start command. Participants will be instructed to touch the pods with the hand being tested to turn off the lights as quickly as possible and to maintain this throughout the test.

    3. Left/Right Judgment Task [Day 1]

      The Left/Right Discrimination Ability (LRJT) Task test will be performed using the Recognize® tablet application (RecogniseTM application, NOI, Neuro-orthopedic Institute). The Recognize hand assessment kit tablet version iPad (9.7 inch, iPad, Apple Computers) will be downloaded and used.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion criteria:
    • being between 18 and 35 years of age

    • having normal upper extremity function

    • having a Montreal Cognitive Assessment Test (MoCA) score > 26 points

    Exclusion criteria:
    • any neuromuscular or musculoskeletal disease

    • history of upper limb injury

    • upper limb surgery within the last 6 months

    • body mass index (BMI) > 30 kg/m2.

    Contacts and Locations

    Locations

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

    Sponsors and Collaborators

    • Ilke KARA

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ilke KARA, Co-Principal Investigator, Dokuz Eylul University
    ClinicalTrials.gov Identifier:
    NCT06004635
    Other Study ID Numbers:
    • BEU-KTS-02
    First Posted:
    Aug 22, 2023
    Last Update Posted:
    Aug 22, 2023
    Last Verified:
    Aug 1, 2023
    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 Ilke KARA, Co-Principal Investigator, Dokuz Eylul University

    Study Results

    No Results Posted as of Aug 22, 2023