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
48 participants
INTERVENTIONAL
2023-12-01
2024-08-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Intervention Group Electrical Dry Needling amd Physiotherapy
The intervention group will receive a treatment composed by electrical dry needling and conventional physiotherapy treatment
Electrical dry needling + Conventional physiotherapy
Electrical dry needling and conventional physiotherapy treatment (massage, pressure release): 2 sessions
Intervention Group Dry Needling amd Physiotherapy
This group will receive a treatment composed by dry needling and conventional physiotherapy treatment
Dry needling + Conventional physiotherapy
Dry needling and conventional physiotherapy treatment (massage, pressure release): 2 sessions
Control Group
Control group will receive conventional physiotherapy treatment
Conventional physiotherapy
Conventional physiotherapy treatment (massage, pressure release): 2 sessions
Interventions
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Electrical dry needling + Conventional physiotherapy
Electrical dry needling and conventional physiotherapy treatment (massage, pressure release): 2 sessions
Dry needling + Conventional physiotherapy
Dry needling and conventional physiotherapy treatment (massage, pressure release): 2 sessions
Conventional physiotherapy
Conventional physiotherapy treatment (massage, pressure release): 2 sessions
Eligibility Criteria
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Inclusion Criteria
* federated and non-federated of Castilla y León
* playing tennis for at least 2 years
* presence if one trigger point in epicondilar musculature
Exclusion Criteria
* nervous, vascular, articular or musculoskeletal system alterations
* tests or techniques performed fear (belonephobia)
* pregnancy
* allergic to any type of metal or body oil
* active febrile proces
* current pain treatments in the area involved
* surgery in the last year for upper limb pathologies
* cognitive alterations
* taking painkillers or anti-inflammatory drugs 24 hours before the start of the study or taking them during the duration of the study
16 Years
65 Years
ALL
Yes
Sponsors
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University of Salamanca
OTHER
Responsible Party
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Rocío Llamas-Ramos
Associate Professor
Locations
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Universidad de Salamanca
Salamanca, Salamanca, Spain
Countries
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Other Identifiers
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EMGepicondíleos
Identifier Type: -
Identifier Source: org_study_id