Visual Aids for Colonoscopy Preparation: A Prospective Study on Patient Understanding and Bowel Cleanliness in Colonoscopy Patients
NCT ID: NCT07155603
Last Updated: 2025-09-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
120 participants
INTERVENTIONAL
2025-09-30
2028-12-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
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Traditional Consent (Control Group)
The traditional informed consent process involves the provision of written documents and verbal explanation to the patient regarding the colonoscopy procedure, risks, and preparation requirements
Animated Video Group 1
The animated video intervention provides a clear and engaging multimedia explanation of the colonoscopy procedure in multiple languages. It includes visual aids to help explain the process, preparation instructions, risks, and expected outcomes, aiming to improve patient comprehension and adherence.
Animated Video 1
Patients of this group will be asked to watch the Visikon animated videos, in addition to receiving standard informed consent
Animated Video Group 1
The animated video intervention provides a clear and engaging multimedia explanation of the colonoscopy procedure in multiple languages. It includes visual aids to help explain the process, preparation instructions, risks, and expected outcomes, aiming to improve patient comprehension and adherence.
Interventions
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Animated Video Group 1
The animated video intervention provides a clear and engaging multimedia explanation of the colonoscopy procedure in multiple languages. It includes visual aids to help explain the process, preparation instructions, risks, and expected outcomes, aiming to improve patient comprehension and adherence.
Eligibility Criteria
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Inclusion Criteria
* Scheduled for a routine outpatient colonoscopy procedure
* Capable of understanding communication in German and willing to participate in the study
Exclusion Criteria
* Those unwilling to participate
18 Years
ALL
No
Sponsors
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Prof. Dr. Jörg Leuppi
OTHER
Responsible Party
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Prof. Dr. Jörg Leuppi
Prof. Dr. med. Jörg Daniel Leuppi
Locations
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Cantonal Hospital of Baselland
Liestal, , Switzerland
Countries
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Facility Contacts
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Other Identifiers
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2024-01572
Identifier Type: -
Identifier Source: org_study_id
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