The Impact of Paramedic Training in Simulation on the Experience of Patients Treated for Malignant Brain Tumors in Neurosurgery

Status: Recruiting
Location: See all (11) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to demonstrate that simulation training for paramedical staff in neurosurgery departments, in announcing and accompanying patients with a brain tumor, improves patient satisfaction when a (potentially malignant) brain tumor is discovered, compared with usual care. The main question it aims to answer is: \- Are patients more satisfied (as measured by scores on the EORCT IN-PATSAT32 questionnaire) with their neurosurgical hospitalization following the discovery of a brain tumor in centers where paramedics have been trained by simulation? Researchers will compare the results of the EORTC IN-PATSAT32 questionnaire to determine whether paramedic training improves patient satisfaction between simulation-trained and untrained centers. Participants will be asked to complete the EORT IN-PATSAT32 questionnaire at the end of their hospital stay.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient over 18 years of age

• Patient covered by a social security scheme

• Patient signed informed consent form

• Patient found to have a brain tumor (potentially malignant, primary or secondary if this is the mode of entry into the disease)

• Hospitalization in the Neurosurgery Department at the time of tumor discovery, before the histological diagnosis is announced.

Locations
Other Locations
France
CHU Amiens
NOT_YET_RECRUITING
Amiens
CHU Angers
NOT_YET_RECRUITING
Angers
CHU Bordeaux
NOT_YET_RECRUITING
Bordeaux
CHU Brest
NOT_YET_RECRUITING
Brest
APHM Nord
NOT_YET_RECRUITING
Marseille
CHU Nantes
NOT_YET_RECRUITING
Nantes
CHU Nice
NOT_YET_RECRUITING
Nice
CHU Rouen
NOT_YET_RECRUITING
Rouen
CHU Saint Etienne
RECRUITING
Saint-etienne
CHU Strasbourg
NOT_YET_RECRUITING
Strasbourg
CHU Tours
NOT_YET_RECRUITING
Tours
Contact Information
Primary
Doriane Gautier
doriane.gautier@chu-brest.fr
+33 229 020 174
Backup
Generic address
promotion-interne@chu-brest.fr
+ 33 230 338 340
Time Frame
Start Date: 2025-05-15
Estimated Completion Date: 2026-03
Participants
Target number of participants: 250
Treatments
No_intervention: Standard of care
Centers whose paramedics will not follow the training proposed by the study.
Experimental: Paramedic training
Centers whose paramedics will benefit from the training proposed by the study.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Brest

This content was sourced from clinicaltrials.gov