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Myofascial Induction Effects on Stabilometry Versus Sham Laser

M

Mayuben Private Clinic

Status

Completed

Conditions

Foot Diseases
Myofascial Pain

Treatments

Other: Myofascial Induction
Other: Sham Laser

Study type

Interventional

Funder types

Other

Identifiers

NCT04628286
2111201814518 C

Details and patient eligibility

About

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)

Enrollment

36 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

36 participants in 2 patient groups, including a placebo group

Sham Laser
Placebo Comparator group
Description:
Placebo laser application in plantar fascia
Treatment:
Other: Sham Laser
Experimental group Myofascial Induction
Experimental group
Description:
Myofascial Induction technique application in plantar fascia
Treatment:
Other: Myofascial Induction

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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