- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06396741
Changes in the Quadriceps Muscle After Dry Needling Treatment
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Madrid
-
Alcalá de Henares, Madrid, Spain, 28805
- Centro Investigación Fisioterapia y Dolor
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Study Chair: Samuel Fernandez-Carnero, PhD, Centro de Investigación Fisioterapia y Dolor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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