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Effects on Plantar Support After Deep Dry Needling in Posterior Tibial Muscle

Not Applicable
Completed
Conditions
Movement Disorders
Interventions
Procedure: Deep dry needling in tibialis posterior
Procedure: 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
Inclusion Criteria
  • presence of myofascial trigger point in the posterior tibialis
  • Accept participation in the study (signature of informed consent)
  • Do not present any exclusion criteria
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
GroupInterventionDescription
Deep dry needling in tibialis posteriorDeep dry needling in tibialis posteriorDeep dry needling will be applied in the tibialis posterior myofascial trigger point
Sham technique in tibialis posteriorSham technique in tibialis posteriorPlacebo tibialis dry needling
Primary Outcome Measures
NameTimeMethod
Pain pressure threshold72 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
NameTimeMethod
baropodometric measurements: footprint72 hours

The investigator will be collected maximum pressure point in the footprint (g / cm)

baropodometric measurements: Average footprint pressure72 hours

The investigator will be collected the average footprint pressure (g/cm)

baropodometric measurements: forefoot area72 hours

The investigator will be collected the forefoot area (cm)

baropodometric measurements:forefoot load72 hours

The investigator will be collected the forefoot load (%)

baropodometric measurements: forefoot pressure variation72 hours

The investigator will be collected the forefoot pressure variation (%)

baropodometric measurements: rearfoot support surface72 hours

The investigator will be collected the rearfoot support surface (cm)

baropodometric measurements: hindfoot load72 hours

The investigator will be collected the hindfoot load ( %)

baropodometric measurements: areas of maximum pressure between the foot lines72 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

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