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Search / Trial NCT06956664

Exercise Therapy After Caudal Epidural Steroid Injection

Launched by ÇANKIRI KARATEKIN UNIVERSITY · May 1, 2025

Trial Information

Current as of July 24, 2025

Recruiting

Keywords

Caudal Epidural Injection Low Back Pain Exercise Therapy Aerobic Exercise Core Stabilization

ClinConnect Summary

This clinical trial is exploring the benefits of two different types of exercise programs for people who have received a caudal epidural steroid injection (CESI) for back pain caused by a herniated disc. The trial aims to find out if adding moderate aerobic exercise or core-stabilization exercises to standard physiotherapy can help reduce pain and improve daily functioning better than physiotherapy alone. Participants will take part in a six-week program, starting two weeks after their injection, where they will be randomly assigned to one of three groups: conventional physiotherapy only, physiotherapy plus aerobic exercise, or physiotherapy plus core-stabilization exercises.

To be eligible for the study, participants should be adults aged 18 to 70 who have had an MRI confirming a herniated disc and have experienced ongoing pain after their CESI. They must also be cleared by their doctor to take part in moderate exercise and be able to attend physiotherapy sessions three times a week. Throughout the trial, participants will complete questionnaires and receive support from physiotherapists, with follow-ups to see how their pain and quality of life change over time. This study could help shape better recovery plans for individuals dealing with similar back issues in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age 18 to 70 years.
  • MRI-confirmed lumbar intervertebral disc herniation.
  • Has received a caudal epidural steroid injection (CESI) within the past 2 weeks at Çankırı State Hospital.
  • Low-back or leg pain intensity ≥ 3 cm on a 10-cm Visual Analogue Scale after the injection.
  • Medically cleared for moderate aerobic and core-stabilisation exercise (no cardiac or orthopaedic contraindications).
  • Able to attend supervised physiotherapy three times per week for six weeks.
  • Willing and able to give written informed consent and to comply with study procedures.
  • Sufficient Turkish literacy (minimum primary-school education) to complete questionnaires.
  • Exclusion Criteria:
  • Uncontrolled systemic disease (e.g., poorly controlled diabetes mellitus, congestive heart failure, active hepatitis C or other significant liver disease).
  • Neurological red flags such as myelopathy or cauda equina syndrome.
  • Previous lumbar spine surgery at the affected disc level.
  • Current pregnancy or planning pregnancy during the study period.
  • Severe musculoskeletal, cardiovascular, or respiratory condition that precludes safe exercise participation.
  • Use of systemic corticosteroids or opioid analgesics that cannot be stabilised for the duration of the trial.
  • Ongoing litigation or workers' compensation claim related to low-back pain.
  • Inability to communicate effectively with study staff or to follow instructions.

About çankırı Karatekin University

Çankırı Karatekin University is a distinguished academic institution committed to advancing medical research and clinical innovation. With a strong emphasis on interdisciplinary collaboration, the university actively engages in clinical trials that aim to enhance healthcare outcomes and contribute to the scientific community. Leveraging its state-of-the-art facilities and a network of experienced researchers, Çankırı Karatekin University fosters a rigorous research environment dedicated to exploring novel therapeutic approaches and improving patient care. The university's commitment to ethical standards and regulatory compliance ensures that all clinical trials conducted under its auspices uphold the highest levels of integrity and scientific excellence.

Locations

çankırı, , Turkey

çankırı, , Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported