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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02919150
Other study ID # 134a
Secondary ID
Status Completed
Phase N/A
First received September 27, 2016
Last updated October 18, 2017
Start date November 1, 2016
Est. completion date July 31, 2017

Study information

Verified date November 2016
Source University of Castilla-La Mancha
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date July 31, 2017
Est. primary completion date July 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
University of Castilla-La Mancha Hospital Nacional de Parapléjicos de Toledo, Universidad San Jorge

Outcome

Type Measure Description Time frame Safety issue
Primary Inter-rater reliability of myotonometric measurement 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
Primary Correlation between myotonometric measurement and isokinetic measurement Relationships among myotonometric parameters and isokinetic parameters Day 1
Primary Sensitivity of distinguishing the localisation of myofascial trigger points within the taut band Ability to identify and differentiate myofascial trigger points and other points within the taut band using the myotonometer Day 1
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