Evaluation of Patient Information in Interventional Radiology.

April 10, 2024 updated by: Centre Hospitalier Universitaire de Saint Etienne

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

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • France
      • Saint-Étienne, France
        • Recruiting
        • CHU Saint-Etienne
        • Sub-Investigator:
          • Rémi Grange, MD
        • Principal Investigator:
          • Sylvain Grange, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Any patient who receives a consultation before an interventional procedure will be included.

Description

Inclusion Criteria:

  • Any patient who receives a consultation before an interventional procedure.

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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.).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist
Time Frame: Year : 2
Analysis results of questionary.
Year : 2
To evaluate Effectiveness of each patient information tool by Consultation with another doctor who explained the procedure
Time Frame: Year : 2
Analysis results of questionary.
Year : 2
To evaluate Effectiveness of each patient information tool by Explanatory videos
Time Frame: Year : 2
Analysis results of questionary.
Year : 2
To evaluate Effectiveness of each patient information tool by Patient information sheet
Time Frame: Year : 2
Analysis results of questionary.
Year : 2
To evaluate Effectiveness of each patient information tool by Posters in the consultation room
Time Frame: Year : 2
Analysis results of questionary.
Year : 2

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centre Hospitalier Universitaire de Saint Etienne

Investigators

  • Principal Investigator: Sylvain GRANGE, MD, CHU Saint-Etienne

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2021

Primary Completion (Estimated)

January 1, 2025

Study Completion (Estimated)

January 1, 2025

Study Registration Dates

First Submitted

February 27, 2023

First Submitted That Met QC Criteria

March 9, 2023

First Posted (Actual)

March 13, 2023

Study Record Updates

Last Update Posted (Actual)

April 11, 2024

Last Update Submitted That Met QC Criteria

April 10, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • IRBN1482021/CHUSTE

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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