Condition: Intervertebral Disc Displacement · Low Back Pain · Radiculopathy · Sponsor: Çankırı Karatekin University
\*\*Brief Summary\*\* Lumbar radicular pain arising from intervertebral disc herniation is commonly managed with a caudal epidural steroid injection (CESI), a minimally invasive procedure that delivers anti-inflammatory medication to the sacral hiatus. Although CESI affords short-term analgesia, a sizable proportion of patients continue to experience pain-related disability and diminished quality of life, underscoring the need for optimised post-injection rehabilitation. This single-centre, three-arm, parallel-group randomised controlled trial will evaluate the comparative efficacy of two evidence-informed exercise paradigms-moderate-intensity aerobic training and progressive lumbopelvic stabilisation-when each is superimposed upon a standard physiotherapy package of heat, therapeutic ultrasound and transcutaneous electrical nerve stimulation (TENS). Forty-two adults (18-70 years) with MRI-confirmed lumbar disc herniation who have undergone CESI at Çankırı State Hospital will be randomly allocated (1:1:1) to one of the following six-week interventions, initiated two weeks post-injection and delivered thrice weekly under physiotherapist supervision: 1. Conventional physiotherapy alone (heat + ultrasound + TENS). 2. Conventional physiotherapy plus aerobic exercise (treadmill walking at 55-80 % of age-predicted maximal heart rate with structured warm-up/cool-down). 3. Conventional physiotherapy plus core-stabilisation exercise (phased activation of deep trunk musculature prog…
This description comes directly from the study's public registry record.
Ceyhun Türkmen, PhD · +90 376 218 95 00 · ceyhunturkmen@karatekin.edu.tr
Always discuss trial participation with your own doctor first.
| Çankırı Karatekin University | Çankırı, Turkey (Türkiye) | Active Not Recruiting |
| Çankırı State Hospital | Çankırı, Turkey (Türkiye) | Recruiting |
| Çankırı State Hospital | Çankırı, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06956664