Miodural Bridge Stretching in Posture Modification in Professional Footballers

Investigación en Hemofilia y Fisioterapia

Status: Withdrawn

Conditions: Hamstring Injury

Treatments: Other: Manual therapy

Study type: Interventional

Funder types: NETWORK

Identifiers

NCT04290065

POST

Details and patient eligibility

About

Fatigue influences the kinematics of the knee. Decreasing the tone of the suboccipital musculature may decrease the tone of the knee flexors. Inhibition of the suboccipital musculature is used to improve ischiosural muscle tension.

The main objective of the study is to evaluate the effectiveness of the stretching of the miodural bridge in the modification of the posture in professional soccer players of 3rd division.

Randomized clinical trial. 30 players will be randomized to the two study groups: experimental (technique of stretching technique of the miodural bridge) and control (without intervention). A blinded evaluator will perform three evaluations: pretreatment, post-treatment and follow-up. The study variables will be: modification of posture and weight distribution (plantar pressure platform). The sample distribution will be calculated using a Kolmogórov-Smirnov analysis. The changes after each evaluation will be analyzed with the t-student test of related samples and through an ANOVA of repeated measures the intra and intersubject effect will be observed. The effect size will be calculated using Cohen's formula.

After stretching the miodural bridge, it is expected to see improvement in posture changes.

Sex: Male

Ages: 18 to 23 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Football players
• Male
• From 18 to 23 years old
• That have a federation file in 3rd division in the Region of Murcia
• That you don't have any acute lesions at the time of the study.

Exclusion criteria

• Subjects that: present some relevant subacute or chronic pathology that may have a direct impact on the processes or structures related to the study who have neurological problems or related to the vestibular system
• That receive a specific Physiotherapy training on any of the study regions
• Not sign the informed consent document

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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0 participants in 2 patient groups

Experimental group

Experimental group

Description:

The intervention will take place over a period of 4 weeks, with 2 weekly sessions, with an estimated execution time of 1.50 to 3 minutes each. A manual therapy technique of inhibition of the suboccipital musculature and an axial traction of the upper hemiarchy will be performed

Treatment:

Other: Manual therapy

Control group

No Intervention group

Description:

Athletes included in the control group will not perform any intervention, continuing with their usual routine.