Tecar Therapy in Patients With Lumbar Radiculopathy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorIzmir City Hospital

About this trial

Lumbar radiculopathy is a common cause of low back and leg pain, most frequently resulting from lumbar disc herniation and nerve root irritation. Conservative management, including physical therapy modalities and exercise therapy, is generally recommended as first-line treatment for patients without progressive neurological deficits. Tecar therapy (Transfer of Energy Capacitive and Resistive) is a non-invasive electrotherapeutic modality that delivers high-frequency electromagnetic energy to deep tissues and has been proposed to reduce pain, enhance microcirculation, and promote tissue recovery. However, evidence regarding its effectiveness in lumbar radiculopathy remains limited.

The aim of this randomized controlled trial is to evaluate the efficacy of Tecar therapy in patients with lumbar radiculopathy and to compare its clinical effects with conventional physical therapy and sham Tecar treatment.

A total of 90 participants with unilateral L5 and/or S1 radiculopathy will be randomized into three groups: (1) conventional physical therapy, (2) Tecar therapy combined with standard physical therapy, and (3) sham Tecar therapy combined with standard physical therapy. All participants will receive standardized postural education and a home exercise program.

The primary outcome will be pain intensity measured by the Visual Analog Scale (VAS). Secondary outcomes will include functional disability (Oswestry Disability Index), neuropathic pain characteristics (PainDETECT questionnaire), lumbar mobility (Modified-Modified Schober Test), nerve root irritability (Straight Leg Raise test), rescue analgesic consumption, and exercise adherence. Outcomes will be assessed at baseline, post-treatment (week 2), and follow-up visits at weeks 6 and 12.

Eligibility criteria

Qualifiers

Adults aged 18-65 years

Clinical diagnosis of unilateral L5 and/or S1 lumbar radiculopathy

Symptom duration between 6 weeks and 6 months

Average radicular pain intensity ≥3 on the Visual Analog Scale (VAS) during the previous month

Disqualifiers

Bilateral lumbar radiculopathy

Lumbar spinal canal stenosis confirmed by imaging or suspected clinically (e.g., neurogenic claudication)

Lower limb muscle strength <4/5 according to the Medical Research Council (MRC) scale

Use of analgesic medications other than paracetamol during the study period

Trial design

Treatments tested in this trial

  • Tecar Therapy
  • Sham Tecar Therapy
  • Conventional Physical Therapy

Treatment groups

90 Participants
are divided into 3 treatment groups

Sponsors and collaborators