Clinical trial Recruiting at 1 site Interventional Ages 18 to 55

Cervical Epidural Block With or Without Exercises for Chronic Neck Pain

Official title: Comparison of Cervical Epidural Block Alone Versus Combined Treatment Modalities in Chronic Neck Pain

Run by Sakarya University · NCT07787741 · Data updated 2026-11-12

This study tests whether adding cervical stabilization exercises or physical therapy to a cervical epidural block helps reduce neck pain and improve function in adults with chronic neck pain and cervical radiculopathy.

Quick facts

Study typeInterventional
Ages18 Years to 55 Years
SexAll
Enrollment60 (estimated)
SponsorSakarya University
Academic / other
Locations1 site (Adapazarı, Sakarya)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedOctober 1, 2027
Study endsOctober 1, 2027
Registry record updatedSeptember 8, 2026
Trial IDNCT07787741 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–55 with chronic neck pain (>3 months) and cervical radiculopathy who score 5 or higher on the pain scale.

Probably not a fit

Patients with prior spinal surgery, certain spinal conditions, systemic diseases, or contraindications to the procedures may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares three treatment approaches for chronic neck pain due to cervical disc pathology or degeneration. Participants receive a cervical epidural steroid injection alone, the injection plus a cervical stabilization exercise program, or the injection plus a physical therapy program. Outcomes include pain intensity, neck-related disability, and quality of life measured at baseline, 1, 3, and 6 months using the Numeric Rating Scale, Neck Disability Index, and the 12-Item Short Form Health Survey. The trial seeks to determine if adding structured exercise or therapy to the block provides additional benefit over the block alone. The study is conducted at Sakarya Training and Research Hospital in Sakarya, Turkey, with 18- to 55-year-old adults recruited based on specific chronic neck pain and radiculopathy criteria.

Why it matters

Potential benefit: If successful, patients may experience greater pain relief and improved neck function by combining therapy with the block.

How similar studies have gone: Limited direct comparisons exist; this three-arm design addresses a gap by evaluating additive effects of exercise/therapy to the block.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged 18 to 55 years
* Neck pain lasting longer than 3 months
* Diagnosis of cervical radiculopathy
* Numeric Rating Scale (NRS) pain score of 5 or higher

Exclusion Criteria:

* History of spinal surgery
* Cervical spondylolisthesis
* Spinal stenosis
* Presence of a neurological deficit
* History of psychiatric disease
* Polyneuropathy
* History of spinal fracture
* Pregnancy
* History of malignancy
* Known allergy to any medication used in the study
* Central sensitization
* Widespread pain
* Regional pain associated with a systemic disease

Where it's running

  • Sakarya Training and Research Hospital
    Adapazarı, Sakarya, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: KEMAL NAS, MD, Professor — Sakarya University Training and Research Hospital, Department of Algology
  • Study coordinator: Yunus Türkyilmaz, Md
  • Email: yunusturkyilmaz54@gmail.com
  • Phone: +905415096040

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.