Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2019-03-10
2019-06-20
Brief Summary
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Aim. To evaluate the efficacy of an intervention by electrotherapy combined with myofascial therapy, in the lumbar region, for a mobility improvement in older paddle-tennis federated players.
Study design. Randomized, multicenter, simple blind, clinical trial with follow-up period.
Methods. 30 players paddle will be assigned to the two study groups: experimental (intervention through therapy myofascial and electrotherapy) and control (intervention by electrotherapy). The intervention will have a duration of 4 weeks, with 2 sessions per week, lasting 15 minutes. There will be three evaluations: pre-intervention, post-intervention and follow-up. The variable of study is the mobility of the lumbar spine in the movements of flexion and extension (assessed by the employment of tests of Schober and Fingertip-to-floor). The analysis of normality be performed with the Kolmogorov-Smirnof, and in case of homogeneity of the groups is used in parametric tests: test t-student for paired data (difference between the different assessments) and ANOVA of mean repeated (intra-and intersujeto).
Expected results. Improvement of the mobility of the lumbar spine in the movements of flexion and extension.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Myofascial
The subjects that include the experimental group will receive an intervention through myofascial therapy of crossed hands and electrotherapy
Myofascial
The aim of the application of the crossed hands technique is to produce a deep fascial release, placing the subject in prone position, while the standing physiotherapist will contact with one hand on the spine at the level of the thoracolumbar hinge and with the other hand on the sacrum, so that the hands are crisscrossed. The crossed hands technique will be performed between 90 seconds and 5 minutes.
The application of the TENS, will be performed for 10 minutes by means of a device, model Compex in the lumbar area, subjects will receive a TENS application of low frequency (less than 40Hz). The electrode - (black) in proximal position or on the most painful zone. The electrode + (red) will be placed distally.
Electrotherapy
The subjects that are included in the experimental group will receive an intervention through electrotherapy
Electrotherapy
The application of the TENS, will be performed for 10 minutes by means of a device, model Compex in the lumbar area, subjects will receive a TENS application of low frequency (less than 40Hz). The electrode - (black) in proximal position or on the most painful zone. The electrode + (red) will be placed distally.
Interventions
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Myofascial
The aim of the application of the crossed hands technique is to produce a deep fascial release, placing the subject in prone position, while the standing physiotherapist will contact with one hand on the spine at the level of the thoracolumbar hinge and with the other hand on the sacrum, so that the hands are crisscrossed. The crossed hands technique will be performed between 90 seconds and 5 minutes.
The application of the TENS, will be performed for 10 minutes by means of a device, model Compex in the lumbar area, subjects will receive a TENS application of low frequency (less than 40Hz). The electrode - (black) in proximal position or on the most painful zone. The electrode + (red) will be placed distally.
Electrotherapy
The application of the TENS, will be performed for 10 minutes by means of a device, model Compex in the lumbar area, subjects will receive a TENS application of low frequency (less than 40Hz). The electrode - (black) in proximal position or on the most painful zone. The electrode + (red) will be placed distally.
Eligibility Criteria
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Inclusion Criteria
* With federal sheet
* Male
* Over 18 years
* Currently participate in regional and / or national competitions
Exclusion Criteria
* Not signed the informed consent document.
18 Years
MALE
Yes
Sponsors
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Investigación en Hemofilia y Fisioterapia
NETWORK
Responsible Party
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Principal Investigators
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Rubén Cuesta-Barriuso, PhD
Role: PRINCIPAL_INVESTIGATOR
Universidad Europea de Madrid
Locations
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Universidad Europea de Madrid
Madrid, Comunity of Madrid, Spain
Countries
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Other Identifiers
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MIOTENS
Identifier Type: -
Identifier Source: org_study_id
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