Evaluation of Patient Information in Interventional Radiology.
Sponsor
Centre Hospitalier Universitaire de Saint Etienne (Other)
Overall Status
Recruiting
CT.gov ID
NCT05765799
Collaborator
(none)
100
1
25
4
Study Details
Study Description
Brief Summary
Interventional radiology is developing. Patient information modalities are also evolving, in particular information videos.
The aim of this work is therefore the evaluation of patient information in interventional radiology
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Patient Information in Interventional Radiology.
Actual Study Start Date
:
Dec 1, 2021
Anticipated Primary Completion Date
:
Jan 1, 2024
Anticipated Study Completion Date
:
Jan 1, 2024
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Patient who receives a consultation before an interventional procedure Any patient who receives a consultation before an interventional procedure will be included. Questionary will be administrated. |
Other: Questionary
Questionary will be administrated to evaluated the information for patients on interventional radiology (dedicated consultation, information posters, explanatory video, information form, etc.).
|
Outcome Measures
Primary Outcome Measures
- To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist [Year : 2]
Analysis results of questionary.
- To evaluate Effectiveness of each patient information tool by Consultation with another doctor who explained the procedure [Year : 2]
Analysis results of questionary.
- To evaluate Effectiveness of each patient information tool by Explanatory videos [Year : 2]
Analysis results of questionary.
- To evaluate Effectiveness of each patient information tool by Patient information sheet [Year : 2]
Analysis results of questionary.
- To evaluate Effectiveness of each patient information tool by Posters in the consultation room [Year : 2]
Analysis results of questionary.
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- Any patient who receives a consultation before an interventional procedure.
Exclusion Criteria:
- None
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Chu Saint-Etienne | Saint-Étienne | France |
Sponsors and Collaborators
- Centre Hospitalier Universitaire de Saint Etienne
Investigators
- Principal Investigator: Sylvain GRANGE, MD, CHU SAINT-ETIENNE
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Centre Hospitalier Universitaire de Saint Etienne
ClinicalTrials.gov Identifier:
NCT05765799
Other Study ID Numbers:
- IRBN1482021/CHUSTE
First Posted:
Mar 13, 2023
Last Update Posted:
Mar 13, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier Universitaire de Saint Etienne