Effects of Diacutaneous Fibrolysis Over Neuromuscular Response

NCT ID: NCT03963674

Last Updated: 2019-05-28

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-05

Study Completion Date

2019-06-05

Brief Summary

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The study consists in evaluating the neuromuscular response of the gastrocnemious muscles before and after a diacutaneous fibrolysis over the gastrocnemious muscles.

Detailed Description

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Conditions

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Myofascial Pain Syndrome Contraction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Diacutaneous fibrolysis

Group Type EXPERIMENTAL

Diacutaneous fibrolysis

Intervention Type OTHER

Diacutaneous fibrolysis over the gastrocnemious muscles

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Diacutaneous fibrolysis

Diacutaneous fibrolysis over the gastrocnemious muscles

Intervention Type OTHER

Eligibility Criteria

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Exclusion Criteria

* Muscle injury in the last two months
* To not understand the study orders
* Suffer a musculoskeletal disorder that doesn't allow the subject to do the study protocol
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universitat Internacional de Catalunya

OTHER

Sponsor Role lead

Responsible Party

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Albert Pérez Bellmunt

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Albert Pérez-Bellmunt

Sant Cugat del Vallès, Barcelona, Spain

Site Status

Countries

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Spain

Other Identifiers

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Protocol 5

Identifier Type: -

Identifier Source: org_study_id

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