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

NCT ID: NCT02919150

Last Updated: 2017-10-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-11-01

Study Completion Date

2017-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Muscle Tone Abnormalities

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Myofascial Trigger Points Myotonometry Isokinetic Dynamometry Assessment Reliability

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Hospital Nacional de Parapléjicos de Toledo

OTHER

Sponsor Role collaborator

Universidad San Jorge

OTHER

Sponsor Role collaborator

University of Castilla-La Mancha

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Julio Gomez Soriano, PhD

Role: STUDY_DIRECTOR

University of Castilla-La Mancha

Carolina Jiménez Sánchez, MSc

Role: PRINCIPAL_INVESTIGATOR

Universidad San Jorge

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

134a

Identifier Type: -

Identifier Source: org_study_id