Effects of the Myofascial Induction Technique Versus a Control Laser

Mayuben Private Clinic36 enrolled

Overview

The objective is to determine the effectiveness of myofascial Induction effects on plantar pressures variables. Forty healthy subjects will be recruited for a simple blind clinical trial. All subjects will be randomly distributed in two different groups: control group (sham Laser) and experimental group (myofascial Induction). Outcome measurements will be foot plantar pressure area (footprint) by a validated platform. Two trials will be recorded before and after intervention in standing position.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Foot Diseases Myofascial Pain

Interventions

Sham LaserOTHER

Sham Laser in plantar fascia

Myofascial InductionOTHER

Myofascial Induction in plantar fascia

Eligibility

Sex: ALLMin age: 18 YearsMax age: 40 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy individuals without pain. Exclusion Criteria: * Previous lower extremities surgery * History of lower extremities injury with residual symptoms within the last year * Evidence of a leg-length discrepancy of more than 1 cm * Evidence of balance deficits

Locations (1)

Mayuben Clinic

San Sebastián de los Reyes, Madrid, Spain

Outcomes

Primary Outcomes

Plantar pressure measure

Plantar pressure measure by validated footprint platform in grams / square centimeter

Time frame: Register a plantar pressures of foot print in standing position of 30 seconds

Secondary Outcomes

Plantar surface measure

Area of plantar footprint measure by aa validated footprint platform in square centimeters

Time frame: Register a plantar surface area of foot print in standing position of 30 seconds

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.