Evaluating patient information in interventional radiology
Evaluation of Patient Information in Interventional Radiology
This study is testing different ways to provide information to patients about interventional radiology procedures, like cementoplasty, to see how well they understand their treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Saint Etienne Academic / other |
| Locations | 1 site (Saint-Etienne) |
| Trial ID | NCT06354075 on ClinicalTrials.gov |
What this trial studies
This study evaluates how patient information is provided in interventional radiology, focusing on the effectiveness of various modalities, including information videos. It involves collecting feedback through questionnaires from patients who are consulting for procedures like cementoplasty. The goal is to enhance patient understanding and satisfaction regarding their treatment options. By assessing the current information practices, the study aims to identify areas for improvement in patient communication.
Who should consider this trial
Good fit: Ideal candidates include patients receiving consultations for cementoplasty and children undergoing any interventional radiology procedure.
Not a fit: Patients who are not receiving consultations for interventional radiology procedures may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved patient satisfaction and understanding of interventional radiology procedures.
How similar studies have performed: While there is ongoing research in patient information practices, this specific evaluation of interventional radiology is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patients receiving a consultation prior to a cementoplasty procedure and children receiving a consultation prior to any interventional radiology procedure. Exclusion Criteria: * None
Where this trial is running
Saint-Etienne
- Chu Saint-Etienne — Saint-Etienne, France (Recruiting)
Study contacts
- Principal investigator: Sylvain GRANGE, MD — Centre Hospitalier Universitaire de Saint Etienne
- Study coordinator: Sylvain GRANGE, MD
- Email: Sylvain.Grange@chu-st-etienne.fr
- Phone: (0)477127827
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.