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Clinical Trials in Turkey / NCT07065851
Active, not recruiting Not applicable

Comparison of Shockwave Therapy and Exercise on Pain, Flexibility, and Balance in Hamstring Tightness

NCT07065851 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-10
Last updated
2025-07-25

Condition(s) studied

Low Back PainHamstring Tightness

Investigational drug(s) / intervention(s)

Extracorporeal Shock Wave Therapy (ESWT)Exercise Program

Extracorporeal Shock Wave Therapy (ESWT): Non-invasive therapy delivering high-energy shock waves to stimulate healing in musculoskeletal tissues, targeting the hamstring muscles and related structures, administered 2 times per week for 4 weeks, alongside core exercises.

Exercise Program: Structured exercises focusing on hamstring flexibility, lumbar stabilization, and core exercises, administered 3 times per week for 3 weeks, with sessions lasting 30-45 minutes.

Study summary

This randomized controlled trial aims to compare the short- and long-term effects of extracorporeal shock wave therapy (ESWT) and exercise therapy on pain, flexibility, and balance in individuals with low back pain associated with hamstring tightness. Thirty participants will be randomized into two groups (ESWT or exercise) and receive interventions twice weekly for four weeks. Outcomes include pain (a (VAS), flexibility (Popliteal Angle and Fingertip-to-Floor tests), and balance (Y-Balance Test), assessed at baseline, post-intervention, and at a four-week follow-up.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * • Diagnosed with low back pain due to hamstring tightness. * Aged 18-65 years. * Male or female. * Medically cleared for ESWT or exercise therapy. * Experienced low back pain in the past 6 months without serious spinal pathology (e.g., herniated disc, fracture). Exclusion Criteria: * • Other musculoskeletal conditions causing low back pain (e.g., disc herniation, spinal stenosis). * Outside the specified age range. * Serious health conditions that may affect study outcomes. * Pregnant or breastfeeding women. * Surgical intervention in the back or hamstring region within the past 6 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bahcesehir University Istanbul Healthy

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07065851 on ClinicalTrials.gov ↗ ← All trials in Turkey