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Clinical Trials/NCT04222946
NCT04222946
Completed
Not Applicable

Stabilometry and Plantar Pressures Changes After Bilateral Dry Needling in Flexor Digitoum Brevis.A Pretest Posttest Study.

Mayuben Private Clinic1 site in 1 country18 target enrollmentJanuary 7, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Mayuben Private Clinic
Enrollment
18
Locations
1
Primary Endpoint
Stabilometry variables eyes closed
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this clinical trial is to check the effects of dry needling in the Flexor digitorum Brevis .

Detailed Description

Fiveteen healthy subjects wil be recruited for a quasi-experimental study. Participants will be from 18 to 40 years old, not obese. Participants will be measured before and after bilateral dry neddling in Flexor digitorum Brevis. The investigators will measure stabilometry variables and static footprint. The footprint variables will be divided in bilateral rear foot, bilateral midfoot, bilateral fore foot. Measures. Stabilometry will be measured by displacement of the center of pressures in X and Y with eyes open and closed , center of pressure (COP) with eyes open and closed, COP area with eyes open and closed, COP antero-posterior (a-p) and medio-lateral (m-lat) directions with eyes open and closed, and COP speed. Two trials will be recorded for each condition and the order of the conditions will be randomized across subjects, eyes open and eyes closed. Foot plantar pressure and surface area of two static footprints will be measured during bipedal standing. Static plantar pressure will be evaluated by means of maximum pressure, medium pressure and surface area of each aspect of the foot (rearfoot, midfoot, and fore foot).

Registry
clinicaltrials.gov
Start Date
January 7, 2020
End Date
March 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Mayuben Private Clinic
Responsible Party
Principal Investigator
Principal Investigator

EVA MARIA MARTÍNEZ JIMENEZ

Head of Podiatry, Principal Investigator, and Physiotherapist

Mayuben Private Clinic

Eligibility Criteria

Inclusion Criteria

  • Healthy individuals
  • Must have latent trigger point in Flexor Brevis Digitorum muscles

Exclusion Criteria

  • Previous lower extremities surgery.
  • History of lower extremities injury with residual symptoms (pain, "giving-away" sensations) within the last year.
  • Leg-length discrepancy more than 1 cm
  • Balance deficits (determined by oral questionnaire regarding falls)

Outcomes

Primary Outcomes

Stabilometry variables eyes closed

Time Frame: Through study completion, an average of 1 month

Stabilometry assessment was used and subjects were instructed to stand barefoot on the force platform, participants were instructed to remain in a relaxed standing posture with feet shoulder-width apart and positioned at 30º away from the midline. Stabilometry variables measure displacement of the center of pressures in X and Y with closed eyes, Center of Pressure (COP) area and anteroposterior(a-p) and mediolateral directions: COP speed.

Stabilometry variables eyes open

Time Frame: Through study completion, an average of 1 month

Stabilometry assessment was used and subjects were instructed to stand barefoot on the force platform, participants were instructed to remain in a relaxed standing posture with feet shoulder-width apart and positioned at 30º away from the midline. Stabilometry variables measure displacement of the center of pressures in X and Y with open eyes, Center of Pressure (COP) area and anteroposterior(a-p) and mediolateral directions: COP speed.

Static footprint

Time Frame: Through study completion, an average of 1 month

Static footprint will measure plantar presures and surface area of rear food, midfoot and fore foot. Subjects were instructed to stand barefoot on the force platform, participants were instructed to remain in a relaxed standing posture with feet shoulder-width apart and positioned at 30º away from the midline. During all the examinations, the upper limbs were placed in a relaxed position along the body. The subjects were instructed to stand as still as possible for 30 s, with their eyes open, while concentrating on a point at eye level 2-m away or with their eyes open.

Secondary Outcomes

  • Stabilometry variables eyes closed after intervention(Through study completion, an average of 1 month)
  • Static footprint after intervention(Through study completion, an average of 1 month)
  • Stabilometry variables eyes open after intervention(Through study completion, an average of 1 month)

Study Sites (1)

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