Effects on Plantar Support After Deep Dry Needling in Posterior Tibial Muscle
- Conditions
- Movement Disorders
- Interventions
- Procedure: Deep dry needling in tibialis posteriorProcedure: Sham technique in tibialis posterior
- Registration Number
- NCT03756428
- Lead Sponsor
- Cardenal Herrera University
- Brief Summary
This study aims to analyze the changes in plantar support after the technique of deep dry puncture in the posterior tibial. The data will be analyzed by a baropodometer which will record the possible changes in the footprint. The investigator will perform a pre-intervention measurement and 3 post-intervention measurements (immediately after the intervention, at 24 hours and at 72 hours)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 80
- presence of myofascial trigger point in the posterior tibialis
- Accept participation in the study (signature of informed consent)
- Do not present any exclusion criteria
- Do not present myofascial trigger point in the tibialis posterior.
- Suffering and / or having suffered from lower limb pathologies, deformities or orthopedic injuries that could alter the static and biomechanics.
- Not clearly identify the Myofascial trigger point in the tibialis posterior.
- Have been diagnosed with fibromyalgia, myelopathy or radiculopathy.
- Having contraindicated the technique of dry needling for suffering, for example, coagulation problems.
- Be pregnant.
- Have used analgesics 24 hours before participating in the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Deep dry needling in tibialis posterior Deep dry needling in tibialis posterior Deep dry needling will be applied in the tibialis posterior myofascial trigger point Sham technique in tibialis posterior Sham technique in tibialis posterior Placebo tibialis dry needling
- Primary Outcome Measures
Name Time Method Pain pressure threshold 72 hours Amount of pressure (Kg/cm2) applied at the tibialis posterior myofascial trigger point site that elicit pain for the patient will be reported
- Secondary Outcome Measures
Name Time Method baropodometric measurements: footprint 72 hours The investigator will be collected maximum pressure point in the footprint (g / cm)
baropodometric measurements: Average footprint pressure 72 hours The investigator will be collected the average footprint pressure (g/cm)
baropodometric measurements: forefoot area 72 hours The investigator will be collected the forefoot area (cm)
baropodometric measurements:forefoot load 72 hours The investigator will be collected the forefoot load (%)
baropodometric measurements: forefoot pressure variation 72 hours The investigator will be collected the forefoot pressure variation (%)
baropodometric measurements: rearfoot support surface 72 hours The investigator will be collected the rearfoot support surface (cm)
baropodometric measurements: hindfoot load 72 hours The investigator will be collected the hindfoot load ( %)
baropodometric measurements: areas of maximum pressure between the foot lines 72 hours The investigator will be collected the areas of maximum pressure between the foot lines (g/cm)
Trial Locations
- Locations (1)
Universidad CEU Cardenal Herrera
🇪🇸Valencia, Moncada, Spain