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Comparison of Dry Needle and Massotherapy on Tolerance Effort and Soreness

Not Applicable
Conditions
Delayed Onset Muscle Soreness
Registration Number
NCT03619928
Lead Sponsor
Universidade Federal de Pernambuco
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
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 & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pressure pain threshold48 hours

Algometry

Delayed onset muscle soreness48 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.

Secondary Outcome Measures
NameTimeMethod
Muscle thickness48 hours

Ultrassonography

Temperature48 hours

Thermography

Time limit48 hours

Isometric performance test

Trial Locations

Locations (1)

Romero Souza Leão de Albergaria Crasto

🇧🇷

Recife, Pernambuco, Brazil

Romero Souza Leão de Albergaria Crasto
🇧🇷Recife, Pernambuco, Brazil
Romero SL Crasto
Contact
81992266788
romeroslac@gmail.com

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