Effectiveness of Percutaneous Electrolysis and Dry Needling vs. Standard Therapy for Whiplash Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCamilo Jose Cela University

About this trial

The main objective of this research is to evaluate the effectiveness of two interventions (PIE vs DDN) in adult patients who have suffered a LCS after a traffic accident and comparing it with a standard physiotherapy program. As a secondary objective, the investigators will analyze the reduction of intrafibrillar blood flow and muscle elasticity perceived by the patient in the long term and the reduction of pain and disability appreciated by the patient.

It is hypothesized as an alternative hypothesis that percutaneous electrolysis and/or deep dry needling intervention in combination with standard physiotherapy will give better clinical outcomes in patients with active trigger point LCS following a road traffic accident compared to the current standard physiotherapy intervention.

The researchers will compare both invasive physical therapy techniques with standard treatment to see if these techniques are more effective in treating whiplash syndrome.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults with whiplash syndrome following a traffic accident.

Patients must reside or stay in the Autonomous Community of Melilla during the intervention phase.

Subjects will have the presence of neck pain after suffering a traffic accident and the presence of at least one active trigger point in the sternocleidomastoid and/or levator scapulae muscles.

All subjects who suffer a traffic accident and who have a score of 5 or higher on the numerical scale (EN) of pain assessment.

Disqualifiers

Patients undergoing anticoagulant treatment.

Patients who have suffered previous cervical trauma or who have undergone surgery in the last year.

Subjects who present some type of alteration (skin or infection, sensitivity or pain perception).

Subjects with central or peripheral nervous system involvement.

Trial design

Design model

Parallel

Treatments tested in this trial

  • intratissue percutaneous electrolysis

    Other intervention

    Using fine needles guided by ultrasound to apply electrical stimulation directly to the affected tissue (for example, damaged muscles or tendons).

  • deep dry needling

    Other intervention

    Insertion of fine needles into muscle trigger points (without injection of drugs) to relieve muscle pain and release tension.

  • Standard physiotherapy

    Procedure/Surgery

    It includes manual techniques such as therapeutic massage and mobilization, along with stretching and strengthening exercises to improve range of motion and reduce pain.

Treatment groups

36 Participants
are divided into 3 treatment groups
Group A: standard physiotherapy treatmentActive comparator 1 intervention
Group B: intratissue percutaneous electrolysisExperimental treatment 1 intervention
Group C: Deep Dry needlingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Intrafibrillar blood flow

To assess intrafibrillar blood flow, the ultrasound tool is used, with color Doppler. the hypervascularity of small vessels in the inflamed synovial tissue of the structures is evaluated. Measurements are expressed in liters per minute (l/min).

Time frame
From the beginning of treatment to the end of treatment at 4 weeks and at 3 months
2

Elasticity of muscle fibers

Elastography is used to evaluate the elasticity of muscle fibers. It is a grayscale ultrasound technique that is superimposed on the color parametric image that expresses the rate of tissue deformation.Making it possible to express the stiffness and elasticity of the tissue in units of pressure (kilopascals).

Time frame
From the beginning of treatment to the end of treatment at 4 weeks and at 3 months

Secondary outcomes

1

Pain perceived by the patient

Pain is a quantitative variable. The investigators will use the numerical evaluation scale (EN), which consists of a numbered scale from 1 -10.

Time frame
From the beginning of treatment to the end of treatment at 4 weeks and at 3 months
2

Pain perceived by the patient

Another pain variable is the pressure pain threshold (PPT), which is an unpleasant sensory and emotional experience associated with a present injury and a pressure algometer will be used. Measurements are expressed in kg/cm2.

Time frame
From the beginning of treatment to the end of treatment at 4 weeks and at 3 months
3

Disability

To assess disability, the investigators will use the Whiplash Disability Questionnaire (WDQ) scale. It is the first instrument for patients with whiplash syndrome, which includes items related to areas of life, personal care and work and those related to the perception of pain. This questionnaire consists of 13 items, scored from 0 to 10 points.

Time frame
From the beginning of treatment to the end of treatment at 4 weeks and at 3 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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