- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04475146
Impact of Visualisation an Explanatory Video on the Quality of Bowel Preparation
Impact de la Visualisation d'Une vidéo Explicative Sur la qualité de la préparation Intestinale
Study Overview
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
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Mathias VIDON, MD
- Phone Number: 01 57 02 27 30
- Email: mathias.vidon@chicreteil.fr
Study Contact Backup
- Name: Laurent COSTES, MD
- Phone Number: 01 57 02 27 34
- Email: Laurent.costes@chicreteil.fr
Study Locations
-
-
-
Créteil, France, 94100
- Recruiting
- Centre Hospitalier Intercommunal de Créteil
-
Contact:
- Mathias VIDON, MD
- Phone Number: 01 57 02 27 30
- Email: mathias.vidon@chicreteil.fr
-
Villeneuve-Saint-Georges, France
- Recruiting
- CHI Villeneuve St George
-
Contact:
- Julia ROUX, MD
- Email: julia.roux@chiv.fr
-
Contact:
- Armand Garioud, MD
- Email: armand.garioud@chiv.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
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
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PREPAVIDEO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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