Changes in the Quadriceps Muscle After Dry Needling Treatment

June 1, 2026 updated by: Prof. Dr. Daniel Pecos Martín

Determination of Biomechanical Changes in the Quadriceps Muscle After Dry Needling Treatment

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.

Study Overview

Study Type

Interventional

Enrollment (Actual)

46

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Madrid
      • Alcalá de Henares, Madrid, Spain, 28805
        • Centro Investigación Fisioterapia y Dolor

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy subject.

Exclusion Criteria:

  • Low back pain
  • Hip pain
  • Sciatica
  • Belenophobia
  • Be medicated with anticoagulants
  • Knee surgery
  • Knee osteoarthritis
  • Fibromyalgia
  • Pregnancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Quadriceps muscle dry needling
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle thickness
Time Frame: before and after one week. The muscle thinckness will be measurement in centimeters
Muscle thickness and echo intensity, an indicator of muscle quality, are related to muscle strength, physical function, and muscle mass measured using echographs ultrasound.It will be measured how muscle thickness changes after applying a dry needling technique
before and after one week. The muscle thinckness will be measurement in centimeters

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quadriceps muscle strength
Time Frame: before and after one week.
The quadriceps muscle strength evaluation will be the measurement of isometric knee extension strength with a hand-held dynamometer (microFET2, Hoggan Scientific, LLC; West Jordan, UT). The maximum voluntary contraction of the quadriceps muscle will be measured. The participants completed three maximal isometric contractions, holding for approximately 3 seconds, with one minute of rest between each contraction.The value of the force will be obtained by calculating the average of the three measurements. The muscle strength wil be measurement in kilograms
before and after one week.
knee range of motion (flexion)
Time Frame: before and after one week
To measure knee flexion, bend the knee as far as you can, by sliding your foot up towards your buttocks, keeping the arms and axis of the goniometer in place, then measure. Passive Knee Flexion ROM: up to 150º, depending on the size of the leg - the limit is the calf pushing onto the back of the thigh. The knee range of motion will be measurement in degrees
before and after one week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Samuel Fernandez-Carnero, PhD, Centro de Investigación Fisioterapia y Dolor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2025

Primary Completion (Actual)

May 1, 2026

Study Completion (Actual)

May 15, 2026

Study Registration Dates

First Submitted

April 25, 2024

First Submitted That Met QC Criteria

April 29, 2024

First Posted (Actual)

May 2, 2024

Study Record Updates

Last Update Posted (Actual)

June 2, 2026

Last Update Submitted That Met QC Criteria

June 1, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CEID/2022/5/092

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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