- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06004635
Reliability of Myotonometry in the Assessment of Mechanical Properties of Thenar Muscles
May 2, 2024 updated by: Ilke KARA
Reliability and Sex-Based Variations in Myotonometer Assessment of Thenar Muscle Properties: Implications for Grip Strength
This study aimed to (i) assess the reliability of myotonometer measurements in determining the mechanical properties of thenar muscle in healthy individuals and explore gender-based variations in these properties; (ii) examine the relationship between pinch grip strength and these mechanical properties.
Study Overview
Status
Completed
Conditions
Detailed Description
Investigating the mechanical properties of hand muscles using simple applicable methods such as myotonometer 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: to (i) assess the reliability of myotonometer measurements in determining the mechanical properties of thenar muscle in healthy individuals and explore gender-based variations in these properties; (ii) examine the relationship between pinch grip strength and these mechanical properties.
Study Type
Observational
Enrollment (Actual)
40
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
-
-
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Bitlis, Turkey, 13000
- Bitlis Eren University
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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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Healthy adults between 18-35 years old
Description
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.
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 |
|---|---|---|
|
Muscle tone (Hz)
Time Frame: 30 Minutes
|
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.
|
30 Minutes
|
|
Stiffness (N/m)
Time Frame: 30 Minutes
|
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.
|
30 Minutes
|
|
Elasticity (Logarithmic decrement)
Time Frame: 30 Minutes
|
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.
|
30 Minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pinch strength
Time Frame: 30 Minutes
|
Pinch grip strength will be assessed using a hydraulic pinchmeter (Baseline).
Standard procedures recommended by American Society of Hand Therapists (ASHT) will be followed.
|
30 Minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
September 1, 2023
Primary Completion (Actual)
April 1, 2024
Study Completion (Actual)
May 1, 2024
Study Registration Dates
First Submitted
July 24, 2023
First Submitted That Met QC Criteria
August 21, 2023
First Posted (Actual)
August 22, 2023
Study Record Updates
Last Update Posted (Actual)
May 3, 2024
Last Update Submitted That Met QC Criteria
May 2, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- BEU-KTS-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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