- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03964961
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
Status
Unknown
Conditions
Intervention / Treatment
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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