- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03619928
Comparison of Dry Needle and Massotherapy on Tolerance Effort and Soreness
August 2, 2018 updated by: ROMERO SOUZA LEÃO DE ALBERGARIA CRASTO, Universidade Federal de Pernambuco
Comparison of Dry Needle and Massotherapy on Tolerance to the Effort and Soreness of Individuals With Late Muscular Pain Induced by Exercise
Introduction: Delayed onset muscle soreness (DOMS) is a common myogenic condition considered to be a muscle tension injury frequently observed in recreational or experienced athletes, induced in the majority of cases by eccentric and inactive exercises, the most common of which are: tension, pain and impairment muscular and have a course of typical duration of 24 hours and peak between 48 and 72 hours.
Among the treatments proposed with the aim of reducing the symptoms of DOMS is massage therapy.
However, dry needling is a relatively new technique that has been used in myotendinous lesions and its effects on late muscle pain have not yet been studied.
Objective: To compare the impact of dry needling and massage therapy on exercise tolerance, and analgesia of sedentary individuals with late muscle pain induced by eccentric exercise.
The present study is characterized as a randomized and blinded comparative study in which male sedentary individuals will be invited in which the late muscle pain will be induced through eccentric contractions and will receive different treatments: dry needling or massage therapy.
The upper limb functionality, pain perception, superficial hyperemia and brachial biceps thickness will be compared through the exams: visual analogue pain scale (VAS), digital algometry, thermography, ultrasonography and isometric test.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
20
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 Contact
- Name: Romero SL Crasto, Esp.
- Phone Number: 81992266788
- Email: romeroslac@gmail.com
Study Locations
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-
Pernambuco
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Recife, Pernambuco, Brazil, 50670-901
- Recruiting
- Romero Souza Leão de Albergaria Crasto
-
Contact:
- Romero SL Crasto
- Phone Number: 81992266788
- Email: romeroslac@gmail.com
-
-
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 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
not practicing physical activity BMI greater than 18 and less than 30 members of the UFPE community
Exclusion Criteria:
making use of analgesic or anti-inflammatory medications acupuncture or dry needling or massage therapy in the last 6 months report of muscle pain orthopedic neurological problems hypertension and diabetes cardiovascular or respiratory diseases
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Dry needling
Procedure in which a thin needle is used to penetrate the skin, subcutaneous tissues and muscle with the intention of mechanically stimulating the tissue without the use of an anesthetic.
The physiological mechanism supporting the effects of dry needling remains to be clarified.
It has been suggested that the needle works according to the pain gate control theory, indicating that one type of sensory input could be inhibited in the Central nervous system by another input
|
20 minutes through a sterile, disposable Dong Bang® needle size of 0.25X30 mm.
At the moment of insertion of the needle, the therapist will perform a muscular shortening around the application site, in a pincer movement performed by the index and thumb fingers, in order to isolate the muscle fibers of the biceps brachii.
Five needles will be applied to the short head brachii biceps in five points: origin, insertion, center of the muscular womb (60% of the distance from the medial acromion to the cubital fossa in the elbow line) and two points equidistant from the center 2 cm.
|
Active Comparator: Massotherapy
Among the therapeutic approaches for DOMS is massage therapy.
Several authors have examined the effects of DOMS massage and indirect markers of muscle damage, such as impaired muscle function, edema and muscle changes in blood proteins.
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A 20-minute massage will be applied to the non-dominant upper limb exercised by a therapist for the massage condition.
The massage will consist of: 1) surface slip; 2) deep slip; 3) kneading; 4) friction with the thumbs; 5) friction with four fingers; 6) percussions with open and alternating hands; 7) percussions with open and simultaneous hands; 8) tapping; and 9) surface slip.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure pain threshold
Time Frame: 48 hours
|
Algometry
|
48 hours
|
Delayed onset muscle soreness
Time Frame: 48 hours
|
Visual analogue scale which measures the pain and whose minimum value is zero and the maximum value is 100 millimeters.
The higher value is the worse the pain.
|
48 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle thickness
Time Frame: 48 hours
|
Ultrassonography
|
48 hours
|
Temperature
Time Frame: 48 hours
|
Thermography
|
48 hours
|
Time limit
Time Frame: 48 hours
|
Isometric performance test
|
48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Romero SL Crasto, Esp., Master student, program in physical therapy
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 27, 2018
Primary Completion (Anticipated)
August 27, 2018
Study Completion (Anticipated)
October 1, 2018
Study Registration Dates
First Submitted
July 27, 2018
First Submitted That Met QC Criteria
August 2, 2018
First Posted (Actual)
August 8, 2018
Study Record Updates
Last Update Posted (Actual)
August 8, 2018
Last Update Submitted That Met QC Criteria
August 2, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DN, massotherapy and DOMS
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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