Instrumental myofascial release in submission athletes.

Phase 2

Recruiting

• Conditions: Therapeutics; Massage; 55208

• Registration Number: RBR-79jpg98
• Lead Sponsor: Instituto de Pesquisa e Ensino do Hospital HOME

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-11-10
• Study Completion: 2022-06-30
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

Male individuals; age group between 18-40 years; minimum practice time of two years; blue band minimum graduation; average frequency of three weekly training sessions and competitions per year.

Exclusion Criteria

Those who answer YES” to any question on the Physical Activity Readiness Questionnaire (PAR-Q) will not be included; have any inflammatory disease or have taken anti-inflammatory medication during the past four weeks; present neuromuscular disorders; present handgrip strength less than 40 Kgf; and report of musculoskeletal injury in the last six months.
Those who fail to participate in any stage of the study will be excluded.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
A subjective scale of pain perception will be used to evaluate pain intensity immediately, 24 and 48 hours post exercise.

Secondary Outcome Measures

Name	Time	Method
To evaluate muscle damage, molecular markers as kinase creatine (KC) and lactato desidroganase (LDH) levels will be analyzed. To evaluate muscle function, the participants will answer a recovery perception questionnaire and will be measure the maximum voluntary isometric contraction by hand grip.