Myotonometric Measurement of Myofascial Trigger Points: Reliability, Validity and Sensitivity

October 18, 2017 updated by: University of Castilla-La Mancha

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

Completed

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

Observational

Enrollment (Actual)

50

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

14 years to 51 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Subjects must be healthy volunteers and will be recruited from the city of Toledo.

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

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

  • 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

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)

November 1, 2016

Primary Completion (Actual)

July 1, 2017

Study Completion (Actual)

July 31, 2017

Study Registration Dates

First Submitted

September 27, 2016

First Submitted That Met QC Criteria

September 27, 2016

First Posted (Estimate)

September 29, 2016

Study Record Updates

Last Update Posted (Actual)

October 20, 2017

Last Update Submitted That Met QC Criteria

October 18, 2017

Last Verified

November 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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.

Clinical Trials on Muscle Tone Abnormalities

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