Opinions of Healthcare Providers About a European Neuromodulation Register

NCT06030973 | Unknown

• 1 other identifier: PROLOGUE
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this online survey is to gain further insights in the needs and burden for a European registry for neuromodulation, according to healthcare providers.

Conditions

Registry; Neuromodulation; Survey

Outcome Measures

Primary Outcomes (4)

• Healthcare providers their current degree of participation in a registry for neuromodulation.

  Degree of participation in a registry for neuromodulation (question).

  Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.

• Healthcare providers their need for a European registry.

  Underlying reasons on why a European registry is needed, or not needed (question).

  Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.

• Items that should be included in a registry for neuromodulation, according to healthcare providers.

  Items that should be collection within a registry, evaluated with a multiple choice question.

  Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.

• Access regulations to European registry for neuromodulation, according to healthcare providers.

  Access regulations, evaluated with a multiple choice question.

  Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.

Study Arms (1)

Healthcare professionals involved in neuromodulation

Behavioral: Filling in an online survey

Interventions

Filling in an online survey BEHAVIORAL

Professionals are asked to complete questions regarding 1) the degree of current participation in a registry, 2) the need for a European registry, 3) the items that should be collected and 4) access to the European registry.

Healthcare professionals involved in neuromodulation

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

In this study 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) will be eligible to complete the survey. The survey will be spread at the 3ʳᵈ Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg from 31/8/2023 to 2/9/2023.

You may qualify if:

• 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).

You may not qualify if:

• Not involved in management of chronic pain through neuromodulation.

Sponsors & Collaborators

• Moens Maarten: lead
• Vrije Universiteit Brussel: collaborator

Study Sites (1)

Congres Center

Hamburg, Germany

RECRUITING

Central Study Contacts

Maarten Moens

CONTACT

+3224775514; stimulusresearchgroup@gmail.com

Lisa Goudman

CONTACT

+3224775514; stimulusresearchgroup@gmail.com

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: August 26, 2023
• First Posted: September 11, 2023
• Study Start: August 31, 2023
• Primary Completion: September 2, 2023
• Study Completion: September 2, 2023
• Last Updated: September 11, 2023

Record last verified: 2023-09

Locations

DE (1)