ESWT vs Conventional Physical Therapy in Greater Trochanteric Pain Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorKanuni Sultan Suleyman Training and Research Hospital

About this trial

This study aims to compare the effectiveness of Extracorporeal Shockwave Therapy (ESWT) with conventional physical therapy in patients with Greater Trochanteric Pain Syndrome (GTPS). GTPS is a common cause of lateral hip pain, often related to gluteal tendinopathy rather than trochanteric bursitis. Sixty patients will be randomly assigned to two groups: ESWT or conventional physical therapy (TENS, hot pack, ultrasound). Pain (VAS), hip function (Harris Hip Score), lower limb function (LEFS), and global improvement will be evaluated at baseline, week 3, and week 12. The purpose of this study is to determine which treatment provides greater pain relief and functional improvement.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 and 65 years

Lateral hip pain for at least 3 months

Ability to understand study procedures and provide informed consent

Disqualifiers

Hip deformities

Gluteus medius, gluteus minimus, or piriformis tendon tears

Lumbar radiculopathy or history of lumbar spine surgery

Recent trauma or active infection in the hip region

Trial design

Design model

Parallel

Treatments tested in this trial

  • Extracorporeal Shockwave Therapy (ESWT)

    Device

    ESWT applied with Elmed Vibrolith Ortho device at 15 Hz, 3 bar, 2000 pulses, 5 sessions over 3 weeks.

  • TENS; Hot Pack; Ultrasound

    Other intervention

    10 sessions of TENS (20 min), hot pack (20 min), and continuous ultrasound (1.5 W/cm², 5 min).

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: ESWT GroupExperimental treatment 1 intervention
Group B: Conventional Physical Therapy GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in Visual Analog Scale (VAS) Pain Score

Pain intensity will be assessed using a 0-10 Visual Analog Scale (VAS) for activity, rest, and night pain. The primary endpoint is the change in VAS score from baseline to Week 12.

Time frame
Baseline, Week 3, and Week 12

Secondary outcomes

1

Harris Hip Score

Hip function will be evaluated using the Harris Hip Score, which includes pain, daily activities, gait, and range of motion parameters. Higher scores indicate better hip function.

Time frame
Baseline, Week 3, and Week 12
2

Lower Extremity Functional Scale (LEFS)

The LEFS questionnaire will be used to assess lower limb function. It consists of 20 items scored from 0 to 4 (total score 0-80), with higher scores indicating better function.

Time frame
Baseline, Week 3, and Week 12
3

Global Rating of Change (GROC)

Overall patient-perceived improvement will be assessed using the Global Rating of Change Scale, scored from -1 (worse) to +3 (near normal improvement).

Time frame
Week 3 and Week 12

Other outcomes

Sponsors and contacts

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