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NCT04475146 Clinical Trial

Impact of Visualisation an Explanatory Video on the Quality of Bowel Preparation

Colonoscopy Clinical Trial

Official title:
Impact de la Visualisation d'Une vidéo Explicative Sur la qualité de la préparation Intestinale

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04475146
Other study ID # PREPAVIDEO
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2020
Est. completion date March 1, 2024

Study information
Verified date October 2023
Source Centre Hospitalier Intercommunal Creteil
Contact Mathias VIDON, MD
Phone 01 57 02 27 30
Email mathias.vidon@chicreteil.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The research hypothesis is that video visualization improves the quality of bowel preparation and the patients' understanding of the modalities of bowel preparation.

Description:

The prescription of colonoscopy is performed by a gastroenterologist, who chooses the type of bowel preparation. During this consultation, the doctor explains to the patient the bowel preparation, then gives the patient the prescription with the type of product and a sheet explaining the diet without residues. The time between this consultation and the colonoscopy is sometimes long. The idea of this study is to accompany this information on intestinal preparation with a video that details the different stages of intestinal preparation by MOVIPREP. Indeed, studies have in the past shown an improvement in the quality of intestinal preparation with the help of better information to patients (educational booklet, or smartphone application)

Recruitment information / eligibility
Status Recruiting
Enrollment 282
Est. completion date March 1, 2024
Est. primary completion date September 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria - Major patient - Patient with first indication of colonoscopy - Colonoscopy performed in outpatient with preparation by MOVIPREP - Patient affiliated with Social Security - Informed consent signed by the patient Exclusion Criteria: - Hospitalized patients - With no Internet access, or no access to the email - Blind patients - Patient who don't speak French - Pregnant woman - Severe constipation (3 stools/week) or long-term laxatives - History of partial or total colectomy - Other preparation product

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• video vizualisation
video vizualisation

Locations
Country Name City State
France Centre hospitalier intercommunal de Créteil Créteil
France CHI Villeneuve St George Villeneuve-Saint-Georges

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Intercommunal Creteil

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparison of colonoscopy percentage with a Boston score of 7 or higher and a score of 2 or higher in each segment, in group 1 "standard information and video visualization" versus in group 2 "standard information." Boston score Immediately after the colonoscopy
Secondary A scale of understanding and satisfaction in relation to the quality of Information on intestinal preparation. Satisfaction and Understanding Questionnaires (Likert Scale) 2 hours after the colonoscopy
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