Patient-reported outcome registry for spinal conditions and neuromodulation
Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation: a Prospective Real-world Data Collection With Pre-determined Follow-up Moments
This project collects long-term patient-reported outcome data from adults with spinal conditions who receive non-invasive or invasive treatments, including neuromodulation, to see how they do over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Jessa Hospital Academic / other |
| Locations | 1 site (Hasselt, Limburg) |
| Trial ID | NCT07552519 on ClinicalTrials.gov |
What this trial studies
This is a prospective, longitudinal observational registry that collects standardized patient-reported outcome measures and categorical diagnostic and treatment data at predefined follow-up moments for adults treated for spinal pathologies. It captures non-invasive treatments (for example injections and physical therapy), invasive procedures (for example surgery and radiofrequency therapies), and neuromodulation therapies such as spinal cord and DRG stimulation. The program aims to build large-scale outcome data, map patient flow through treatment modalities, and create patient profiles to guide personalized treatment strategies. Data will be collected at Jessa Hospital in Hasselt and shared for publication to inform care pathways and long-term response patterns.
Who should consider this trial
Good fit: Adults (≥18 years) with a clinical diagnosis of spinal disease who have an indication for treatment and are willing and able to provide informed consent are eligible.
Not a fit: People under 18, those without a spinal diagnosis, or those unable to provide informed consent or attend required follow-up visits are unlikely to benefit from participation.
Why it matters
Potential benefit: If successful, the registry could help personalize treatment plans and optimize care pathways to improve long-term outcomes for people with spine conditions.
How similar studies have performed: Other spinal outcome and device registries have identified predictors of response and device performance, but comprehensive profiling across all treatment modalities remains relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Clinical diagnosis of spinal disease 2. Clinical indication to perform treatment of this disease 3. willing and capable to provide informed consent 4. Age ≥18 y Exclusion Criteria: not able to provide consent
Where this trial is running
Hasselt, Limburg
- JEssa Ziekenhuis — Hasselt, Limburg, Belgium (Recruiting)
Study contacts
- Study coordinator: Mark Plazier, M.D. PhD.
- Email: mark.plazier@jessazh.be
- Phone: +3211309071
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.