Actively Recruiting
Study to Analyse the Use of a Digital Platform for the Preparation and Follow-up of Patients With Scheduled Outpatients Colonoscopy
Led by Persei Vivarium · Updated on 2025-06-15
225
Participants Needed
1
Research Sites
20 weeks
Total Duration
On this page
Sponsors
P
Persei Vivarium
Lead Sponsor
E
Effice Servicios Para la Investigacion S.L.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial investigation with device is to to analyze the use of the Caaring® digital platform for the preparation and follow-up of scheduled colonoscopy. Colonoscopy is a difficult procedure, and it is estimated that bowel preparation is inadequate in about 25% of patients. The main question it aims to answer is if the use of a digital platform (Caaring®) could be an effective tool for reducing the percentage of inadequate bowel preparations in patients with a scheduled colonoscopy. To this end, the application will provide precise instructions to patients. A prospective, single-center, observational study with software device: The recruitment phase is expected to last two months. Patients will be followed for one month after the colonoscopy and 14 days prior to it. Additionally, measuring patient experience and monitoring adverse effects after a colonoscopy are crucial to improving the safety of colonoscopies and the quality of healthcare, promoting higher quality colonoscopy services. For that to happen, participants must have sufficient technological skills to use a smartphone.
CONDITIONS
Official Title
Study to Analyse the Use of a Digital Platform for the Preparation and Follow-up of Patients With Scheduled Outpatients Colonoscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Signed informed consent
- Patients scheduled for outpatient colonoscopy
- Patients able to complete the study questionnaires
- Patients who regularly use a smartphone
You will not qualify if you...
- Patients enrolled in the population-based colorectal cancer screening program with a positive fecal occult blood test
- Minors or elderly patients (over 80 years of age)
- Patients with prior colorectal surgery
- Patients who, in the opinion of the researcher, will not be able to commit to follow-up or lack adequate technological skills
- Inability to provide adequate informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital Clínic de Barcelona
Barcelona, Barcelona, Spain, 08036
Actively Recruiting
Research Team
R
Roberto Bravo
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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