Comparison of Dry Needle and Massotherapy on Tolerance Effort and Soreness

• ClinicalTrials.gov Identifier: NCT03619928
• Recruitment Status: Unknown
• First Posted: August 8, 2018
• Last Update Posted: August 8, 2018
• Sponsor: Universidade Federal de Pernambuco
• Information provided by (Responsible Party): ROMERO SOUZA LEÃO DE ALBERGARIA CRASTO, Universidade Federal de Pernambuco

Study Description

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.

Condition or disease	Intervention/treatment	Phase
Delayed Onset Muscle Soreness	Device: Dry needling; Device: Massotherapy	Not Applicable

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 20 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double (Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: Comparison of Dry Needle and Massotherapy on Tolerance to the Effort and Soreness of Individuals With Late Muscular Pain Induced by Exercise
• Actual Study Start Date: July 27, 2018
• Estimated Primary Completion Date: August 27, 2018
• Estimated Study Completion Date: October 1, 2018

Arms and Interventions

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	Device: Dry needling; 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.	Device: Massotherapy; 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.

Outcome Measures

Primary Outcome Measures :

1. Pressure pain threshold [ Time Frame: 48 hours ]
   Algometry
2. 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.

Secondary Outcome Measures :

1. Muscle thickness [ Time Frame: 48 hours ]
   Ultrassonography
2. Temperature [ Time Frame: 48 hours ]
   Thermography
3. Time limit [ Time Frame: 48 hours ]
   Isometric performance test

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 45 Years (Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

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

Contacts and Locations

Contacts

Contact: Romero SL Crasto, Esp.; 81992266788; romeroslac@gmail.com

Locations

Brazil

Romero Souza Leão de Albergaria Crasto; Recruiting

Recife, Pernambuco, Brazil, 50670-901

Contact: Romero SL Crasto 81992266788 romeroslac@gmail.com

Sponsors and Collaborators

Universidade Federal de Pernambuco

Investigators

• Principal Investigator: Romero SL Crasto, Esp.; Master student, program in physical therapy

More Information

• Responsible Party: ROMERO SOUZA LEÃO DE ALBERGARIA CRASTO, Principal researcher, Universidade Federal de Pernambuco
• ClinicalTrials.gov Identifier: NCT03619928
• Other Study ID Numbers: DN, massotherapy and DOMS
• First Posted: August 8, 2018
• Last Update Posted: August 8, 2018
• Last Verified: July 2018

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by ROMERO SOUZA LEÃO DE ALBERGARIA CRASTO, Universidade Federal de Pernambuco:

Dry needling; Massotherapy; Delayed onset muscle soreness

Additional relevant MeSH terms:

Myalgia; Muscular Diseases; Musculoskeletal Diseases; Neuromuscular Diseases; Nervous System Diseases; Musculoskeletal Pain; Pain; Neurologic Manifestations