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Myofascial Induction Effects on Stabilometry Versus Sham Laser

NCT ID: NCT04628286

Last Updated: 2020-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-20

Study Completion Date

2020-12-02

Brief Summary

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The objective is to determine the effectiveness of myofascial induction effects on stabilometric variables. Forty healthy subjects will be recruited for a single blind clinical trial. All subjects will be randomly distributed into two different groups: control group (simulated laser) and experimental group (myofascial induction). Result measurements will be performed in the center of the pressure area (stabilometry) using a validated platform. Two trials will be recorded for each condition (eyes closed and eyes open)

Detailed Description

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Conditions

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Foot Diseases Myofascial Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Sham Laser

Placebo laser application in plantar fascia

Group Type PLACEBO_COMPARATOR

Sham Laser

Intervention Type OTHER

Sham Laser in plantar fascia

Experimental group Myofascial Induction

Myofascial Induction technique application in plantar fascia

Group Type EXPERIMENTAL

Myofascial Induction

Intervention Type OTHER

Myofascial Induction in plantar fascia

Interventions

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Sham Laser

Sham Laser in plantar fascia

Intervention Type OTHER

Myofascial Induction

Myofascial Induction in plantar fascia

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Mayuben Private Clinic

OTHER

Sponsor Role lead

Responsible Party

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EVA MARIA MARTÍNEZ JIMENEZ

Head of Podiatry, Principal Investigator, and Physiotherapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Mayuben Clinic

San Sebastián de los Reyes, Madrid, Spain

Site Status

Countries

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Spain

Other Identifiers

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2111201814518 C

Identifier Type: -

Identifier Source: org_study_id