Evaluation of the Effectiveness of Focused Radiofrequency (TECAR) Therapy on Pain, Disability, Function, and Quality of Life in Patients With Lumbar Disc Herniation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-60
SponsorAnkara City Hospital Bilkent

About this trial

Low back pain is a very common health problem in societies, regardless of the underlying cause. Its lifetime prevalence has been reported to be as high as 75-80%. Low back pain negatively affects the quality of life of affected individuals. In addition to diagnostic and treatment costs, it can lead to serious physical disability, resulting in loss of workforce and placing a substantial economic burden on countries. Many different factors play a role in the etiology of low back pain. According to etiology, it can be classified as idiopathic, mechanical, rheumatologic, metabolic, endocrine, infectious, neoplastic, neurologic/psychiatric disorders, and pain of visceral origin. The treatment of low back pain can be classified into medical treatment, physical therapy, percutaneous invasive interventions, and surgical intervention. TECAR therapy is also one of the treatment modalities routinely used in clinical practice. Our aim is to develop more effective physical therapy programs.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Having low back pain lasting longer than 12 weeks

Disqualifiers

None

Trial population

Patients presenting to the outpatient clinic of the Ankara Bilkent City Hospital Physical Therapy and Rehabilitation Hospital.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • TECAR THERAPY

    Device

    TECAR therapy applied by a technician for 20 minutes per session, three days per week, for a total of six sessions

  • TECAR Therapy

    Device

    TECAR therapy is a new and effective treatment modality.

Treatment groups

54 Participants
are divided into 2 treatment groups
Group A: TECAR Therapy1 intervention
Group B: sham TECAR Therapy1 intervention

Trial outcomes

Primary outcomes

1

Visual Analog Scale (VAS)

Zero indicates no pain at all, whereas ten represents the most severe pain imaginable.

Time frame
Up to 1 month after the end of treatment

Secondary outcomes

1

Oswestry Disability Index

The Oswestry Disability Index (ODI) is a standardized questionnaire designed to assess the degree of disability and functional impairment in individuals with lower back pain

Time frame
Up to 1 month after the end of treatment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.