Survey on healthcare providers' views about a neuromodulation registry in Europe
Opinions of Healthcare Providers About a European Neuromodulation Register: an Online Survey
This study is asking healthcare providers about their thoughts and experiences with neuromodulation to help create a registry that improves how chronic pain is treated.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Universitair Ziekenhuis Brussel Academic / other |
| Locations | 1 site (Hamburg) |
| Trial ID | NCT06030973 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather insights from healthcare providers regarding their needs and challenges related to a European registry for neuromodulation. Participants will complete an online survey designed to assess their opinions and experiences in managing chronic pain through neuromodulation techniques. The findings will help inform the development of a registry that could enhance the understanding and application of neuromodulation in clinical practice.
Who should consider this trial
Good fit: Ideal candidates for this study are healthcare providers involved in the management of chronic pain, particularly those specializing in neuromodulation.
Not a fit: Patients who are not involved in the management of chronic pain through neuromodulation will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for chronic pain through better-informed neuromodulation practices.
How similar studies have performed: While this approach is observational and focuses on provider opinions, similar studies have successfully informed registry developments in other medical fields.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male and female adults who are involved in the management of chronic pain and more specifically in neuromodulation for pain (including but not limited to anesthesiologists, neurosurgeons, nurses). Exclusion Criteria: * Not involved in management of chronic pain through neuromodulation.
Where this trial is running
Hamburg
- Congres Center — Hamburg, Germany (Recruiting)
Study contacts
- Study coordinator: Maarten Moens
- Email: stimulusresearchgroup@gmail.com
- Phone: +3224775514
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.