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

Not Applicable

Completed

• Conditions: Movement Disorders

• 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

Study Timeline

• Study First Submitted: 2018-11-21
• Study First Submitted QC: 2018-11-26
• Study First Posted: 2018-11-28
• Status Verified: 2018-12
• Study Start: 2018-12-01
• Primary Completion: 2018-12-05
• Study Completion: 2018-12-11
• Last Update Submitted: 2018-12-12
• Last Update Posted: 2018-12-13

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

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: hindfoot load	72 hours	The investigator will be collected the hindfoot load ( %)
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: 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