Reactibility of Muscle Volume to Ribs Mobilization According to Mojžíšová

March 1, 2023 updated by: Malá Jitka, Charles University, Czech Republic

Reactibility of Muscle Volume to Ribs Mobilization According to L.Mojzisova.

The goal of this study is to evaluate a top-rated Prague rehabilitation school´s method. Part of Prague rehabilitation school is called Mojžíšová Method, which is mainly used for the treatment of back pain and woman´s non-structural sterility. This method offers an original, innovative way, how to mobilize 1.- 7. costo-sternal joints. This type of mobilization is very effective, fast and safe and probably widely used only in the Czech Republic. Mojžíšová method uses the excentric force of patients pectoral muscle, passive stretch and shoulder joint internal rotation. According to Mojžíšová, If one of the ribs joints has dysfunction (limited range of motion), there can be found higher sensitivity of this joint, certain muscle reflex spasm, hypersensitive zones and joint dysfunction. Probably the last study evaluating this method was made in the 1990s.

Study Overview

Status

Completed

Detailed Description

This research aims to analyze the effect of mobilization of 1.-3-ribs joints in a relationship in sensitivity and volume of neck and shoulders muscles. The ultrasonic diagnostic method will be used to evaluate muscle volume before and after mobilization ribs joints. Visual pain scale will be used to evaluate pain during palpation of certain muscles. This research will examine 30 subjects, aged 19-26 years old, which will be divided into the control and the experimental group. Each subject will be in both groups. In the control group, we are going to analyze, if certain neck muscles keep the same volume for 5 minutes during sitting position after ribs mobilization. The control group will evaluate if there are any muscle volume and palpation muscle sensitivity change before and after mobilization of the ribs joints.

Lack of evidence for a relationship between the ribs joints and reflex spasms was the motivation to make this study. During the research, I have found no study, which was aiming to analyze the relationship between the mobilization of ribs joint and reflex muscle spasms.

Subject: Thirty subjects, men and woman, aged from 19 to 26 years old. Each included subject has to be diagnosed with at least one sensitive 1.-3. costo-sternal connection. The study examines the control and the experimental group.

Method: During the entrance diagnostics, the examiner will palpate subject´s 1.-3. costo-sternal connections and certain muscles on the same side of the sensitive connection. Specifically m.scalenus anterior, medius and posterior, sternocleidomastoideus, levator scapulae and trapezius. Those muscles are related to dysfunction of those connections according to Mojžíšová. The subject will rate the sensitivity of those muscles on the visual pain scale (0-10 scale). During palpation, the examiner will be using his index finger. The subject will lay down on their back and turn their head 45 degrees away from the examined side. Then the examiner will use sonograph to evaluate the volume of sternocleidomastoideus, scalenus anterior and medius muscles, on the side, on the side of the sensitive joint. After that, the subject will rest in sitting position for 5 minutes, and then the examiner will use sonograph again to check the volume of those muscles, If there is any volume change without joint mobilization. The subject will be placed in the same position, just as during the first sonographic examination. Those data will be used for the control group.

After this process, the examiner will mobilize 1.-3. costo-vertebral joints, using the Mojžíšová technique. This technique will be done in the sitting position.

Study Type

Observational

Enrollment (Actual)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Praha, Czechia
        • Charles University, Faculty of physical education and sport

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

19 years to 26 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The observed group composed of University students. Healthy population with typical signs of ribs blockage, according to Mojzisova, means hypertension of surrounded muscles.

Description

Inclusion Criteria:

Blockage of first, second and third costovertebral joints and sternocostal distention, hypertension of scalene muscles.

Exclusion Criteria:

Age under 19 and above 26, structural changes and injuries of the cervical spine and upper ribs.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle volume changes after joint mobilization
Time Frame: 30 minutes
Sonography study of muscle volume
30 minutes

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)

December 20, 2020

Primary Completion (Actual)

March 31, 2021

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

December 23, 2020

First Submitted That Met QC Criteria

December 23, 2020

First Posted (Actual)

December 28, 2020

Study Record Updates

Last Update Posted (Actual)

March 2, 2023

Last Update Submitted That Met QC Criteria

March 1, 2023

Last Verified

December 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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.

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