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

Overview

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

Full Title of Study: “Impact de la Visualisation d’Une vidéo Explicative Sur la qualité de la préparation Intestinale”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: September 1, 2023

Detailed 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)

Interventions

  • Other: video vizualisation
    • video vizualisation

Arms, Groups and Cohorts

  • Standard information and video visualization
    • Standard information and video visualization
  • Standard information, no video
    • Standard information, no video

Clinical Trial Outcome Measures

Primary Measures

  • 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.”
    • Time Frame: Immediately after the colonoscopy
    • Boston score

Secondary Measures

  • A scale of understanding and satisfaction in relation to the quality of Information on intestinal preparation.
    • Time Frame: 2 hours after the colonoscopy
    • Satisfaction and Understanding Questionnaires (Likert Scale)

Participating in This Clinical Trial

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

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 80 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Centre Hospitalier Intercommunal Creteil
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Contact(s)
    • Mathias VIDON, MD, 01 57 02 27 30, mathias.vidon@chicreteil.fr

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.