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Instrumental myofascial release in submission athletes.

The effectiveness of instrumental myofascial release to muscle recovery in submission athletes: controlled randomized study.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
REBEC
Registry ID
RBR-79jpg98
Enrollment
Unknown
Registered
2021-11-10
Start date
2021-08-18
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Therapeutics

Interventions

All athletes, before the intervention, will be submitted to a high intensity training for a period of 60 minutes, using sporting gestures of the modality. Experimental group: 70 male submission athlet
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Sponsors

Instituto de Pesquisa e Ensino do Hospital HOME
Lead Sponsor
Instituto de Pesquisa e Ensino do Hospital HOME
Collaborator

Eligibility

Sex/Gender
Male
Age
18 Years to 40 Years

Inclusion criteria

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

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.

Design outcomes

Primary

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

Secondary

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactClara Nazaré
floresclara62@gmail.com61996523962

Outcome results

None listed

Source: REBEC (via WHO ICTRP)