Evaluation of Patient Information in Interventional Radiology.

NCT05765799 | Recruiting

• 1 other identifier: IRBN1482021/CHUSTE
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

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

Conditions

Patient Satisfaction

Keywords

interventional radiology; Information; videos

Outcome Measures

Primary Outcomes (5)

• To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist

  Analysis results of questionary.

  Year : 2

• To evaluate Effectiveness of each patient information tool by Consultation with another doctor who explained the procedure

  Analysis results of questionary.

  Year : 2

• To evaluate Effectiveness of each patient information tool by Explanatory videos

  Analysis results of questionary.

  Year : 2

• To evaluate Effectiveness of each patient information tool by Patient information sheet

  Analysis results of questionary.

  Year : 2

• To evaluate Effectiveness of each patient information tool by Posters in the consultation room

  Analysis results of questionary.

  Year : 2

Study Arms (1)

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

Interventions

Questionary OTHER

Questionary will be administrated to evaluated the information for patients on interventional radiology (dedicated consultation, information posters, explanatory video, information form, etc.).

Patient who receives a consultation before an interventional procedure

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

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

You may qualify if:

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

You may not qualify if:

• None

Sponsors & Collaborators

• Centre Hospitalier Universitaire de Saint Etienne: lead

Study Sites (1)

Chu Saint-Etienne

Saint-Etienne, France

RECRUITING

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and Compliance; Health Behavior; Behavior

Study Officials

• Sylvain GRANGE, MD

  CHU SAINT-ETIENNE

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Sylvain GRANGE, MD

CONTACT

(0)477127827; Sylvain.Grange@chu-st-etienne.fr

Rémi Grange, MD

CONTACT

(0)477127827; Remi.Grange@chu-st-etienne.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 27, 2023
• First Posted: March 13, 2023
• Study Start: December 1, 2021
• Primary Completion: January 1, 2025
• Study Completion: January 1, 2025
• Last Updated: April 11, 2024

Record last verified: 2024-04

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)