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Study to Analyse the Use of a Digital Platform for the Preparation and Follow-up of Patien

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 ai

Condition(s)Outpatient Colonoscopy
StatusRecruiting
Study typeObservational
SummaryThe 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. A
Who can participateInclusion Criteria: * 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 Exclusion Criteria: * 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.
Ages18 Years to 80 Years
SexAll
Lead sponsorPersei Vivarium
LocationsBarcelona, Barcelona, Spain
Start date2025-03-13
NCT IDNCT06916052
Official listinghttps://clinicaltrials.gov/study/NCT06916052

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