Effects of the Myofascial Induction Technique Versus a Control Laser

• Sponsor: Mayuben Private Clinic (Other)
• Overall Status: Completed
• CT.gov ID: NCT04628299
• Collaborator: (none)
• Enrollment: 36
• Location: 1
• Arms: 2
• Actual Duration (Days): 16
• Patients Per Site Per Month: 68.5

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Foot Diseases; Myofascial Pain	Other: Sham Laser; Other: Myofascial Induction	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 36 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Participant)
• Primary Purpose: Treatment
• Official Title: Effects of the Myofascial Induction Technique Versus a Control Laser
• Actual Study Start Date: Nov 16, 2020
• Actual Primary Completion Date: Nov 30, 2020
• Actual Study Completion Date: Dec 2, 2020

Arms and Interventions

Arm	Intervention/Treatment
Placebo Comparator: Sham Laser A non-emission laser will be applied in plantar fascia	Other: Sham Laser; Sham Laser in plantar fascia
Experimental: Experimental group Myofascial Induction Myofascial Induction in plantar fascia	Other: Myofascial Induction; Myofascial Induction in plantar fascia

Outcome Measures

Primary Outcome Measures

1. Plantar pressure measure [Register a plantar pressures of foot print in standing position of 30 seconds]

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

Secondary Outcome Measures

1. Plantar surface measure [Register a plantar surface area of foot print in standing position of 30 seconds]

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

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 40 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Mayuben Clinic	San Sebastián De Los Reyes	Madrid	Spain	28702

Sponsors and Collaborators

• Mayuben Private Clinic

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: EVA MARIA MARTÍNEZ JIMENEZ, Head of Podiatry, Principal Investigator, and Physiotherapist, Mayuben Private Clinic
• ClinicalTrials.gov Identifier: NCT04628299
• Other Study ID Numbers: 2111201814518 B
• First Posted: Nov 13, 2020
• Last Update Posted: Dec 3, 2020
• Last Verified: Nov 1, 2020

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Foot Diseases

Study Results

No Results Posted as of Dec 3, 2020