Assessment of Rigid Corset Use for Spondylodiscitis Patients
Rigid Corset Immobilisation of Patients Suffering From Spondylodiscitis: Practice Assessment
This study looks at how using rigid corsets helps patients with spondylodiscitis and gathers feedback from doctors and patients about their experiences and satisfaction with this treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Clermont-Ferrand Academic / other |
| Locations | 1 site (Clermont-Ferrand) |
| Trial ID | NCT06489977 on ClinicalTrials.gov |
What this trial studies
This observational study surveys the current management practices for patients suffering from spondylodiscitis, focusing on the use of rigid corsets for immobilization. It aims to gather insights from doctors, paramedical staff, and patients regarding the implementation of corset prescriptions and patient compliance. Additionally, the study will evaluate patient satisfaction and understanding of their treatment. The research will also explore variations in management practices based on healthcare professionals' age, training, specialty, and department.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old who are hospitalized with infectious spondylodiscitis at Clermont-Ferrand University Hospital.
Not a fit: Patients under 18, those with non-infectious spinal pathologies, or those unwilling to participate will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the management and treatment outcomes for patients with spondylodiscitis.
How similar studies have performed: While this study focuses on current practices, similar observational studies have shown varying degrees of success in improving patient management strategies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: For patients: * Patients aged over 18, * Patients hospitalised at Clermont-Ferrand University Hospital with infectious spondylodiscitis, * Patient willing to be interviewed. For care workers: \- Doctors, nurses or care assistants involved in the care of patients hospitalised with spondylodiscitis. Exclusion Criteria: For patients : * Minor patients, * Patients wearing a corset for a non-infectious spinal pathology, * Patient refusing to take part in the study. For care workers: \- Doctor, nurse or nursing auxiliary refusing to take part in the study.
Where this trial is running
Clermont-Ferrand
- Chu Clermont Ferrand — Clermont-Ferrand, France (Recruiting)
Study contacts
- Principal investigator: Aurore MIGNE — University Hospital, Clermont-Ferrand
- Study coordinator: Lise LACLAUTRE
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 334.73.754.963
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.