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Myofascial Induction Effects on Plantar Pressures and Stabilometry

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ClinicalTrials.gov Identifier: NCT03997955
Recruitment Status : Active, not recruiting
First Posted : June 25, 2019
Last Update Posted : July 16, 2019
Sponsor:
Information provided by (Responsible Party):
César Calvo Lobo, Universidad de León

Brief Summary:
The objective is to determine the effectiveness of myofascial Induction effects on plantar pressures and stabilometry variables. Forty healthy subjects (28 females and 12 males) will be recruited for a simple blind clinical trial. All subjects will be randomly distributed in two different groups: control group (sham treatment of myofascial Induction) and experimental group (myofascial Induction). Outcome measurements will be foot plantar pressure area (footprint) and center of pressure area (stabilometry) by the Balance Evaluation Systems test. Two trials will be recorded for each condition.

Condition or disease Intervention/treatment Phase
Foot Diseases Myofascial Pain Other: Myofascial induction Other: Sham myofascial induction Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Myofascial Induction Effects on Plantar Pressures and Stabilometry Variables. A Clinical Trial
Actual Study Start Date : June 25, 2019
Estimated Primary Completion Date : August 15, 2019
Estimated Study Completion Date : August 20, 2019

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Experimental group
Myofascial induction
Other: Myofascial induction
Myofascial induction in plantar fascia

Sham Comparator: Control group
Sham myofascial induction
Other: Sham myofascial induction
Sham myofascial induction in plantar fascia




Primary Outcome Measures :
  1. Foot plantar pressure area [ Time Frame: Change from foot plantar pressure area at 2 minutes ]
    Foot plantar pressure area measured by the Balance Evaluation Systems test (squared centimeters)


Secondary Outcome Measures :
  1. Center of pressure area [ Time Frame: Change from center of pressure area at 2 minutes ]
    Center of pressure area measured by the Balance Evaluation Systems test (squared centimeters)



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03997955


Locations
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Spain
Eva María Martínez
Madrid, Spain, 28700
Sponsors and Collaborators
Universidad de León

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Responsible Party: César Calvo Lobo, Principal Investigator, Universidad de León
ClinicalTrials.gov Identifier: NCT03997955     History of Changes
Other Study ID Numbers: Myofascial-Induction_CT
First Posted: June 25, 2019    Key Record Dates
Last Update Posted: July 16, 2019
Last Verified: July 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Foot Diseases
Musculoskeletal Diseases
Skin Diseases