Effect of TECAR on Cervical Radiculopathy

Delta University for Science and Technology

Status: Not yet enrolling

Conditions: Cervical Radiculopathy

Treatments: Device: TECAR therapy; Device: Sham TECAR therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT07289607

P.T.REC/012/005936

Details and patient eligibility

About

Cervical radiculopathy is characterized by pain, sensory disturbances, and impaired neuromuscular control due to nerve root compression. Proprioception dysfunction is often an overlooked component of this condition and can affect balance, posture, and motor control.

TECAR (Transfer of Energy Capacitive and Resistive) therapy is a form of deep heat electrotherapy known to improve tissue perfusion and neuromuscular function. Although TECAR is widely used for pain relief and mobility, its role in improving proprioception remains under-investigated, especially in cervical conditions. This study aims to bridge this gap by assessing proprioceptive outcomes in patients with cervical radiculopathy receiving TECAR therapy.

Full description

• Design: Randomized controlled trial.
• Groups:
• Control group: Receives standard physiotherapy (e.g., cervical traction, exercises).
• Experimental group: Receives TECAR therapy in addition to standard physiotherapy.
• Duration: 3 sessions per week for 4 weeks.
• Outcome Measures: Joint position sense (JPS) using cervical repositioning tests, pain (VAS), functional disability (NDI).
• Assessment Times: Baseline and after 4 weeks.

Enrollment: 80 estimated patients

Sex: All

Ages: 30 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• • Diagnosed cervical radiculopathy confirmed by clinical and radiological findings

  • Age 30-40 years
  • Pain duration > 4 weeks

Exclusion criteria

• • Cervical fracture or surgery

  • Vestibular disorders
  • Rheumatologic or neurological diseases
  • Cognitive impairment or pregnancy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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80 participants in 2 patient groups

study group

Active Comparator group

Description:

Receives TECAR therapy in addition to standard physiotherapy.

Treatment:

Device: TECAR therapy

Control group

Sham Comparator group

Description:

Receives sham TECAR

Treatment:

Device: Sham TECAR therapy