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
• Status: Recruiting
• 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
• 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

Related Conditions & MeSH terms

• Colonoscopy

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