Changes in the Quadriceps Muscle After Dry Needling Treatment

NCT ID: NCT06396741

Last Updated: 2025-06-03

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-02

Study Completion Date

2025-12-15

Brief Summary

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The present study aims to examine the mechanical changes following dry needling of the quadriceps muscle.

To this end, structural and mechanical changes in quadriceps muscle activity will be measured using M-mode ultrasound.

The quadriceps muscle strength will also be assessed with dynamometry. In addition, the knee joint range will be checked by means of a goniometry procedure.

The subjects will be assessed before and after the application of a dry needling technique on the quadriceps muscle to determine possible changes in the measured variables.

Detailed Description

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Conditions

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Muscle Tightness Muscle Strain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Quadriceps muscle dry needling

The Quadriceps muscle will be punctured with ultrasound control

Group Type EXPERIMENTAL

The quadriceps muscle will be punctured with ultrasound control

Intervention Type OTHER

With the subject in the supine position, the quadriceps muscle will be shown by ultrasound. Subsequently, a dry needling technique will be performed at the most hyperalgesic point using ultrasound control.

Interventions

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The quadriceps muscle will be punctured with ultrasound control

With the subject in the supine position, the quadriceps muscle will be shown by ultrasound. Subsequently, a dry needling technique will be performed at the most hyperalgesic point using ultrasound control.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy subject.

Exclusion Criteria

* Low back pain
* Hip pain
* Sciatica
* Belenophobia
* Be medicated with anticoagulants
* Knee surgery
* Knee osteoarthritis
* Fibromyalgia
* Pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Prof. Dr. Daniel Pecos Martín

OTHER

Sponsor Role lead

Responsible Party

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Prof. Dr. Daniel Pecos Martín

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Samuel Fernandez-Carnero, PhD

Role: STUDY_CHAIR

Centro de Investigación Fisioterapia y Dolor

Locations

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Centro Investigación Fisioterapia y Dolor

Alcalá de Henares, Madrid, Spain

Site Status

Countries

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Spain

Other Identifiers

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CEID/2022/5/092

Identifier Type: -

Identifier Source: org_study_id

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