Effects of Myofascial Induction Pressure Pain Threshold in Trigger Points of the Proximal Muscles of Gastrocnemius

July 28, 2024 updated by: EVA MARIA MARTÍNEZ JIMENEZ, Mayuben Private Clinic

Effects of Myofascial Induction Pressure Pain Threshold in Trigger Points of the Proximal Muscles of Gastrocnemius: A Prepost Study

In the present study we will test the effects of myofascial induction technique in the muscles close to the application in the gastrocnemius muscle.

Study Overview

Detailed Description

In the present study we will test the effects of myofascial induction technique on nearby muscles. The calf maneuver proposed by Pilat for myofascial induction will be applied and the effects on the pain pressure threshold of the trigger points of the flexor digitorum brevis biceps femoris extensor digitorum longus muscles will be observed.

Study Type

Interventional

Enrollment (Actual)

13

Phase

  • Not Applicable

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

    • Madrid
      • San Sebastián De Los Reyes, Madrid, Spain, 28702
        • Mayuben Clinic

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  • Subjects aged 18-39 years.
  • Healthy subjects with trigger point 1 of the gastrocnemius muscle in both lower limbs.

Exclusion criteria;

  • Diagnosis of lower limb injury, including any tendinopathy, bursitis, ligamentous involvement and/or fasciitis.
  • History of lower limb surgery or history of lower limb injury with residual symptoms (pain or sensation of sensation) within the last year.
  • Participants could not have undergone ankle stretching or any other treatment.
  • Diabetes due to possible impaired distal arterial circulation.
  • Foot deformity, cavus and flat feet.
  • Foot deformities such as hammertoes and hallux valgus,
  • plantar calluses.
  • Dysfunction of the lower extremities or chronic injuries.

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

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: Myofascial induction in gastrocnemius
A 3-pass shallow leg gliding technique was applied first, followed by 5 minutes of the deep myofascial calf induction technique described by Pilat.
A 3-pass shallow leg gliding technique was applied first, followed by 5 minutes of the deep myofascial calf induction technique described by Pilat.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1.Pressure pain threshold in flexor digitorum brevis, biceps femoris, extensor digitorum brevis muscles before intervention
Time Frame: Immediately before intervention.
The pressure at which the patient begins to feel pain with pressure is measured 3 times with an algometer. It is measured in newtons.
Immediately before intervention.
2.Pressure pain threshold in flexor digitorum brevis, biceps femoris, extensor digitorum brevis muscles after intervention
Time Frame: Immediately after the intervention.
The joint range is measured in dorsiflexion of the ankle joint with the knee extended under load and is measured with an inclinometer in degrees.Measured in grades.
Immediately after the intervention.

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)

July 22, 2024

Primary Completion (Actual)

July 24, 2024

Study Completion (Actual)

July 28, 2024

Study Registration Dates

First Submitted

July 7, 2024

First Submitted That Met QC Criteria

July 11, 2024

First Posted (Actual)

July 12, 2024

Study Record Updates

Last Update Posted (Actual)

July 30, 2024

Last Update Submitted That Met QC Criteria

July 28, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2911202021420B

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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