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NCT04628299 Clinical Trial

Effects of the Myofascial Induction Technique Versus a Control Laser

Myofascial Pain Clinical Trial

Official title:
Effects of the Myofascial Induction Technique Versus a Control Laser

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04628299
Other study ID # 2111201814518 B
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 16, 2020
Est. completion date December 2, 2020

Study information
Verified date November 2020
Source Mayuben Private Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date December 2, 2020
Est. primary completion date November 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Sham Laser
Sham Laser in plantar fascia
• Myofascial Induction
Myofascial Induction in plantar fascia

Locations
Country Name City State
Spain Mayuben Clinic San Sebastián De Los Reyes Madrid

Sponsors (1)
Lead Sponsor Collaborator
Mayuben Private Clinic

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Plantar pressure measure Plantar pressure measure by validated footprint platform in grams / square centimeter Register a plantar pressures of foot print in standing position of 30 seconds
Secondary Plantar surface measure Area of plantar footprint measure by aa validated footprint platform in square centimeters Register a plantar surface area of foot print in standing position of 30 seconds
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