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

October 24, 2023 updated by: Centre Hospitalier Intercommunal Creteil

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

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

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

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)

Study Type

Observational

Enrollment (Estimated)

282

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

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 to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

All major patients, without legal protection measures, understanding French and having access to the internet and an email address. Patient having a first outpatient colonoscopy with preparation by MOVIPREP.

The study will be proposed by the investigator to patients followed for colonoscopy in the department of Hepato-gastroenterology. If patients accepted to participate in the protocol and the informed consent form is signed, patients will be included in the protocol.

Description

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 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
Standard information and video visualization
video vizualisation
Standard information, no video

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
Immediately after the colonoscopy

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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)
2 hours after the colonoscopy

Collaborators and Investigators

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

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)

September 1, 2020

Primary Completion (Actual)

September 1, 2023

Study Completion (Estimated)

March 1, 2024

Study Registration Dates

First Submitted

July 2, 2020

First Submitted That Met QC Criteria

July 16, 2020

First Posted (Actual)

July 17, 2020

Study Record Updates

Last Update Posted (Actual)

October 25, 2023

Last Update Submitted That Met QC Criteria

October 24, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • PREPAVIDEO

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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