Effect of Functional Massage in Neuromuscular Response.

May 23, 2019 updated by: Albert Pérez Bellmunt, Universitat Internacional de Catalunya

Effect of Functional Massage in Gastrocnemious Muscles Neuromuscular Response

The study compares the effects of two types of massage: a conventional massage and a functional massage, in the neuromuscular response of the gastrocnemious muscles.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

30

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

    • Barcelona
      • Sant Cugat Del Vallès, Barcelona, Spain, 08195
        • Universitat Internacional de Catalunya

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Exclusion Criteria:

  • Muscle injury in the last two months
  • To not understand the study orders
  • Suffer a musculoskeletal disorder that doesn't allow the subject to do the study protocol

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Functional massage
It's a massage combined with a stretching of the muscles.
Active Comparator: Conventional massage
It's a regular massage made with the therapist's hands.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Delay time change
Time Frame: 2 minutes before the intervention, and 8 minutes after the intervention
Time between an electric impulse and 10% of the contraction of the muscle that is being excited with an electric impulse, using an electromyography test (miliseconds).
2 minutes before the intervention, and 8 minutes after the intervention
Contraction time change
Time Frame: 2 minutes before the intervention, and 8 minutes after the intervention
Time between 10% and 90% of the contraction of the muscle that is being excited with an electric impulse, using an electromyography test (miliseconds).
2 minutes before the intervention, and 8 minutes after the intervention
Sustain time change
Time Frame: 2 minutes before the intervention, and 8 minutes after the intervention
time between 50% of the contraction and 50% of the relaxation of the muscle after being impulsed with an electric impulse, using an electromyography test (miliseconds).
2 minutes before the intervention, and 8 minutes after the intervention
Relaxation time change
Time Frame: 2 minutes before the intervention, and 8 minutes after the intervention
time between 90% and 50% of the relaxation of the muscle after being impulsed with an electric impulse, using an electromyography test (miliseconds).
2 minutes before the intervention, and 8 minutes after the intervention
Maximal displacement change
Time Frame: 2 minutes before the intervention, and 8 minutes after the intervention
Maximal displacement of the muscle after being excited with an electric impulse, using an electromyography test (miliseconds).
2 minutes before the intervention, and 8 minutes after the intervention
Relaxation change
Time Frame: 5 minute before the intervention, and 5 minute after the intervention
Time for a muscle to recover its shape from deformation after the removal of an external force, using a "Myoton" (miliseconds).
5 minute before the intervention, and 5 minute after the intervention
Stiffness change
Time Frame: 5 minute before the intervention, and 5 minute after the intervention
Resistance to an external force that deforms its initial shape, using a "Myoton" (N/m).
5 minute before the intervention, and 5 minute after the intervention
Elasticity change
Time Frame: 5 minute before the intervention, and 5 minute after the intervention
Capacity to recover its initial shape after the removal of the external force that lead to its deformation, using a "Myoton" (logarithmic decrement of the tissue's oscillation).
5 minute before the intervention, and 5 minute after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gastrocnemious strength change
Time Frame: 8 minutes before the intervention, and 2 minutes after the intervention
Isometric strength of the gastrocnemious muscles using a handheld dynamometer "microFET 2" (newtons).
8 minutes before the intervention, and 2 minutes after the intervention
Passive ankle dorsiflexion change
Time Frame: 6 minutes before the intervention, and 4 minutes after the intervention
Passive range of motion of the ankle dorsiflexion, using an inclinometer (degrees).
6 minutes before the intervention, and 4 minutes after the intervention
Jump height change
Time Frame: 10 minutes before the intervention, and 1 minute after the intervention
Maximum jump height with one leg using the application "My Jump 2" (centimeters).
10 minutes before the intervention, and 1 minute 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)

February 5, 2019

Primary Completion (Anticipated)

June 5, 2019

Study Completion (Anticipated)

June 5, 2019

Study Registration Dates

First Submitted

May 23, 2019

First Submitted That Met QC Criteria

May 23, 2019

First Posted (Actual)

May 28, 2019

Study Record Updates

Last Update Posted (Actual)

May 28, 2019

Last Update Submitted That Met QC Criteria

May 23, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Protocol 6

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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