Effects of Myofascial Induction Therapy on Pressure Pain and Ankle Range of Motion.

NCT ID: NCT05711745

Last Updated: 2023-02-10

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

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-06

Study Completion Date

2023-02-09

Brief Summary

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In this study, it will be assessed if there are changes in ankle dorsiflexion and pressure pain after performing the myofascial induction technique in the calf.

Detailed Description

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Conditions

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Fascia Trigger Point Pain, Myofascial Range of Motion Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

A pre-post study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Myofascial induction in gastrocnemius

A 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat.

Group Type EXPERIMENTAL

Calf myofascial technique

Intervention Type PROCEDURE

A 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat.

Interventions

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Calf myofascial technique

A 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Subjects with no pain and with 18 to 30 years old.

Exclusion Criteria

* (1) Diagnosis of lower limb injury, including any tendinopathy, bursitis, ligamentous involvement or fasciitis ,
* (2) history of lower limb surgery ,
* (3) participants were required not to have undergone ankle stretching or any other treatment,
* (4) diabetes due to possible alteration of arterial distal circulation,
* (5) deformities of the toes, such as hammer toes and hallux valgus. All subjects signed an informed consent form before participating in the study
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 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

Fisioterapist responsible area

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Eva María Martinez Jiménez

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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2911202021420A

Identifier Type: -

Identifier Source: org_study_id

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