Skip to main content
OpenTrials
Completed

NCT Number: 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

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. 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

  2. Correlation between myotonometric measurement and isokinetic measurement

    Time frame: Day 1

    Relationships among myotonometric parameters and isokinetic parameters

  3. 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

Sponsors and collaborators

Lead sponsor

University of Castilla-La Mancha

Other

Collaborators

  • Hospital Nacional de Parapléjicos de Toledo
  • Universidad San Jorge

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Sep 29, 2016
Registry last updated
Oct 20, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.