- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02919150
Myotonometric Measurement of Myofascial Trigger Points: Reliability, Validity and Sensitivity
The aims of this study are:
- To examine the inter-rater reliability to assess myofascial trigger points using a myotonometer
- To determinate the strength of the correlation between myotonometric parameters and isokinetic parameters
- To evaluate the sensitivity of myotonometric measurements to detect the location of myofascial trigger points
Study Overview
Status
Conditions
Detailed Description
Previous researches have used complicated and expensive methods to measure mechanical properties of muscle tone like isokinetic dynamometer.
The purpose of this investigation is to establish the reliability, validity and sensitivity of a myotonometer to assess myofascial trigger points. The results of this study will verify the inter-reliability of a myotonometer device in order to evaluate muscle tone, examine correlations and associations between myotonometric measurements and isokinetic measurements and provide a measurable understanding of the location of myofascial trigger points.
Assessment:
Myoton device is a simple and portable tool to obtain quantitative and objective assessments of mechanical properties of muscle tone.
Isokinetic dynamometric technique is considered a valid biomechanics method to measure muscle tone in non-injured subjects but isokinetic machine is a heavy and expensive equipment.
Outcome measures:
Myotonometric measures will include muscle frequency, decrement (elasticity) and stiffness.
Isokinetic measures will include passive resistive torque to ankle dorsiflexion and dorsiflexion passive range of motion (PROM)
All outcome measures will be evaluated once.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age range 18-55 years.
- Healthy volunteers.
- Presence of a latent medial MTrP of the soleus muscle.
- Being able to provide written informed consent.
- Being able to follow instructions and realize clinical tests.
Exclusion Criteria:
- Any history of ipsilateral lower limb severe injury or intervention (e.g. fracture, surgical intervention).
- Pain or musculoskeletal injury, ligament injury, tendonitis or plantar fasciitis in the ipsilateral leg for six months previous to the evaluation.
- Peripheral or central nervous system neurological disease.
- Altered sensitivity in the studied area.
- Treatment of a myofascial trigger point in the sural triceps in the six months previous to the evaluation.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
|
Myotonometric and isokinetic measurement
Myotonometric assessment: into the site of the latent medial myofascial trigger point of the soleus muscle and distal to the lateral medial myofascial trigger point of the soleus muscle but into the same taut band. Isokinetic assessment: triceps surae muscle tone will be quantified by measuring the passive range of motion for ankle dorsiflexion and the resistance to passive ankle dorsiflexion at slow and fast velocity. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inter-rater reliability of myotonometric measurement
Time Frame: Day 1
|
In order to study the interrater reliability of the myoton, two different evaluators assess the muscle tone within two marked points using the myotonometer
|
Day 1
|
|
Correlation between myotonometric measurement and isokinetic measurement
Time Frame: Day 1
|
Relationships among myotonometric parameters and isokinetic parameters
|
Day 1
|
|
Sensitivity of distinguishing the localisation of myofascial trigger points within the taut band
Time Frame: Day 1
|
Ability to identify and differentiate myofascial trigger points and other points within the taut band using the myotonometer
|
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 134A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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