Comparing neuromodulation and exercise for chronic neck pain
Comparison of Percutaneous Neuromodulation and Therapeutic Exercise in Patients With Nonspecific Chronic Neck Pain: A Randomized Clinical Trial
This study is testing whether a new type of nerve treatment or exercise works better to help people aged 30 to 65 with long-lasting neck pain feel less pain and move better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 30 Years to 65 Years |
| Sex | All |
| Sponsor | Universidad de Almeria Academic / other |
| Locations | 1 site (Almeria) |
| Trial ID | NCT06695949 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of percutaneous neuromodulation compared to therapeutic exercise in patients suffering from non-specific chronic neck pain. Chronic neck pain is a prevalent condition that significantly impacts quality of life, and many individuals do not recover fully from acute episodes. The study will involve patients aged 30 to 65 who have experienced chronic cervical pain for at least three months and are not undergoing other physiotherapy treatments. By comparing these two interventions, the study seeks to determine which approach offers better pain relief and functional improvement.
Who should consider this trial
Good fit: Ideal candidates for this study are males and females aged 30 to 65 with chronic cervical pain lasting three months or more.
Not a fit: Patients with sensory disorders, history of spine surgery, or serious underlying conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective treatment option for patients suffering from chronic neck pain.
How similar studies have performed: Other studies have shown promise in using neuromodulation techniques for pain management, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male and female patients aged between 30 and 65 years with chronic cervical pain. * Chronic cervical pain lasting 3 months or more and not receiving any other type of physiotherapy treatment. Exclusion Criteria: * Patients with sensory and/or coagulation disorders. * History of spine surgery, cardiac complications, and severe concurrent central or peripheral nervous system disease. * Epilepsy, needle phobia, disc pathology, or serious pathologies that may be the primary cause of chronic cervical pain (e.g., tumors, Arnold Chiari disease, vertigo syndrome, etc.) * Contraindications for transcutaneous electrical nerve stimulation (TENS).
Where this trial is running
Almeria
- University of Almeria — Almeria, Spain (Recruiting)
Study contacts
- Principal investigator: Adelaida María Castro-Sánchez, PhD — Universidad de Almeria
- Study coordinator: Adelaida María Castro-Sánchez, PhD
- Email: adelaid@ual.es
- Phone: +34950214576
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.