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NCT Number: NCT07438392

Tecar Therapy in Chronic Knee Osteoarthritis

This study aimed to investigate the effects of Tecar therapy on pain, physical function, and physical capacity in patients with chronic knee osteoarthritis.

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Key information

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kırşehir Ahi Evran Üniversitesi

Kırşehir, Turkey (Türkiye)

Location contact

Nazife Kapan Tunçer, Asst. Prof.

CONTACT

[email protected]

03862803924

About this study

Knee osteoarthritis is a degenerative, inflammatory, and chronic joint disease with an increasing incidence and prevalence worldwide. By causing pain, disability, and deterioration in quality of life, it constitutes a significant public health problem globally. Furthermore, the health, social, and economic burdens associated with chronic knee osteoarthritis are expected to increase in the future. For these reasons, and due to the rising incidence of the disease, clinicians are increasingly focusing on novel treatment strategies.

Currently, both surgical and non-surgical treatment modalities are used in the management of chronic knee osteoarthritis. The cornerstone of treatment consists of patient education, exercise, and weight control. Subsequent steps include pharmacological treatments, intra-articular injections, and physical therapy modalities. These modalities include transcutaneous electrical stimulation, therapeutic ultrasound, thermal modalities, laser therapy, extracorporeal shock wave therapy, electromagnetic field therapy, and capacitive and resistive electric transfer (Tecar therapy).

Tecar therapy is an endogenous diathermy modality that operates in the long-wave range using radiofrequency energy of approximately 0.5 MHz to heat the treated tissues. It consists of two electrodes-capacitive and resistive-with a long-wave current generator and multi-frequency sequential emission systems that deliver energy to tissues in two different modes. In the capacitive mode, an insulated electrode with a metal plate is generally used. The electrical charges generated by the radiofrequency generator accumulate near the insulated electrode, which acts as a dielectric surface. This method is used for the treatment of superficial tissues adjacent to the insulated electrode. In the resistive mode, two metal electrodes distribute electrical charges that tend to accumulate near bone, tendon, and connective tissue.

Tecar therapy has been shown to have positive effects on pain and quality of life in many patients with degenerative and inflammatory orthopedic conditions. Among diathermy modalities, Tecar therapy is considered one of the most appropriate and safe methods, as-unlike ultrasound-it has no limitation in terms of treatment area and does not cause excessive heat accumulation between the skin and the electrode .

To the best of our knowledge, there are very few studies investigating the use of Tecar therapy in chronic knee osteoarthritis. Therefore, the aim of this study was to investigate the effects of Tecar therapy on pain, physical function, and physical capacity in patients with chronic knee osteoarthritis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with Kellgren-Lawrence stage 2 or 3 knee osteoarthritis
  • Patients with bilateral knee pain for at least 6 weeks
  • Male and female patients aged 40-75
  • Patients who accept and sign the informed consent form

Exclusion criteria

  • Those who have received physical therapy for knee pain in the last 6 months
  • Those who have received intraarticular injection treatments such as hyaluronic acid, PRP, or steroids for knee pain in the last 6 months
  • Those who have undergone knee surgery for any reason
  • Those with inflammatory arthritis
  • Those with existing neurological, cognitive, or psychiatric disorders
  • Those with pacemakers
  • Those with a history of malignancy
  • Those with local vascular or sensory impairment
  • Those with local or systemic infections
  • Those with open wounds on the skin
  • Pregnant or breastfeeding

Treatment and study plan

Tecar Therapy

Other

Tecar Therapy and conventional physical therapy

ShamTecar Therapy

Other

ShamTecar Therapy and conventional physical therapy

Conventional physical therapy

Other

conventional physical therapy

Primary outcomes

  1. Visual Analog Scale

    Time frame: baseline, 3th week, 12th week

    VAS is a pain rating scale with numbers 0 and 10. Here 0 means 'no pain' and 10 means 'unbearable pain'. The participant will rate the pain according to the scale. Patients' night, rest and activity pain will be evaluated separately.

Secondary outcomes

  1. WOMAC

    Time frame: baseline, 3th week, 12th week

    WOMAC consists of three main subgroups: pain, stiffness, and difficulty performing daily activities. It is a questionnaire with a total of 24 questions. Each question has five alternative answers: none, mild, moderate, severe, and very severe. Scoring is given as follows: pain (maximum 20), stiffness (8), and difficulty performing daily activities (68). High scores indicate worsening symptoms, significant limitations, and insufficient overall health. The Turkish version of the scale was developed by Tüzün et al. in 2005.

  2. The 6-minute walk test (6MWT)

    Time frame: baseline, 3th week, 12th week

    The 6-minute walk test (6MWT) will be used to assess physical capacity. Patients will be asked to walk at their preferred pace for 6 minutes in a 30-meter corridor marked at 3-meter intervals. Rest periods or adjustments to walking speed will be allowed if necessary. The maximum distance covered in 6 minutes along the 30-meter corridor will be measured.

Study contacts

Contact information is provided by the study sponsor or research team.

Nazife K Kapan Tunçer, Asst. Prof.

CONTACT

[email protected]

+90 5555839701

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Official study title

Effects of Tecar Therapy (Targeted Radiofrequency Therapy) on Pain, Physical Function, and Physical Capacity in Patients With Chronic Knee Osteoarthritis: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 27, 2026
Registry last updated
Mar 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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