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)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
80
The inspector, with gloves, disinfects the area to be treated with 70º alcohol. Once the alcohol is applied, the intervenor locates and takes the myofascial trigger point and places the needle with the guide tube resting on the skin of the patient. The inspector holds the guide tube between the index and middle fingers lightly touch the needle with the index finger of the other hand to insert the needle perpendicularly into the skin, directing it towards the inspector's thumb. Once the needle is inserted subcutaneously, the guide tube is removed. The controller deepens the needle to myofascial trigger point, and makes fast inputs and outputs into it. The rapid exit is made to the subcutaneous cellular tissue, outside the muscle, but not outside the skin. Next, hemostasis is performed in the area. Once this hemostasis is completed, the patient is incorporated and dressed.
The patient lies on the stretcher without the trousers. The interventor, with the guide tube, simulates the technique of puncture in the right twin of the subject. The comptroller cleans the area with 70º alcohol. Once the alcohol is applied, he performs the simulated dry needling technique in a plane with his index and middle fingers with the guide tube. It is important that the subject has his head stuck in the hollow of the head of the stretcher throughout the technique to make a correct masking.
Universidad CEU Cardenal Herrera
Valencia, Moncada, Spain
Pain pressure threshold
Amount of pressure (Kg/cm2) applied at the tibialis posterior myofascial trigger point site that elicit pain for the patient will be reported
Time frame: 72 hours
baropodometric measurements: footprint
The investigator will be collected maximum pressure point in the footprint (g / cm)
Time frame: 72 hours
baropodometric measurements: Average footprint pressure
The investigator will be collected the average footprint pressure (g/cm)
Time frame: 72 hours
baropodometric measurements: forefoot area
The investigator will be collected the forefoot area (cm)
Time frame: 72 hours
baropodometric measurements:forefoot load
The investigator will be collected the forefoot load (%)
Time frame: 72 hours
baropodometric measurements: forefoot pressure variation
The investigator will be collected the forefoot pressure variation (%)
Time frame: 72 hours
baropodometric measurements: rearfoot support surface
The investigator will be collected the rearfoot support surface (cm)
Time frame: 72 hours
baropodometric measurements: hindfoot load
The investigator will be collected the hindfoot load ( %)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: 72 hours
baropodometric measurements: areas of maximum pressure between the foot lines
The investigator will be collected the areas of maximum pressure between the foot lines (g/cm)
Time frame: 72 hours