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Clinical Trials in Spain / NCT06314022
Recruiting Not applicable

A Mobile Application to Improve the Quality of Colonoscopy in Colorectal Cancer Screening Program (PrepColon APP)

NCT06314022 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2024-05-02
Last updated
2026-06-04

Condition(s) studied

Colorectal CancerPremalignant Colon Lesions

Investigational drug(s) / intervention(s)

Mobile application for colonoscopy preparation instructions

Mobile application for colonoscopy preparation instructions: The APP will also consider the comorbidities and drugs of each patient. It can be adapted to the different types of laxative (4, 2 or 1 litre) and notify the need to discontinue anticoagulant and/or antiplatelet treatments by contacting with the primary care physician. Additionally, the application may ask short questions to the patient to control the laxative intake instruction. The user must confirm the appointment 48 hours in advance.

Study summary

Colonoscopy is the gold standard for the diagnosis and resection of preneoplastic lesions, allowing the prevention of colon cancer. A colonoscopy is more efficient with proper preparation of the colon, as it allows for a higher rate of adenoma detection and cecal intubation. In routine practice, up to 30% of colonoscopies are poorly prepared and 11% of patients do not show up for their appointment. Adenomas not visualized in the initial colonoscopy due to poor preparation reached 68% and the rate of undetected cancers was 66.7%. A proper colon cleanse is conditioned by different factors; among them, failure to comply with the diet and take laxatives poses 5 times the risk of having a deficient colon preparation. The purpose of our study is the design and implementation of an app that facilitates the preparation of colonoscopy and evaluates its impact on compliance with diet and laxative intake.

Eligibility

Sex
ALL
Min age
50 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: * -Subjects between 50-69 years old from the CRC screening program with FIT (\>100ng/ml). * Informed consent granted in writing Exclusion Criteria: * Refusal to give informed consent. * Those who do not have a smartphone with a minimum version of the operating system (Android 4.4 or iOS 14, which cover more than 99% of the terminals in use) * Symptomatic patients * Subjects at elevated risk of CRC due to family history or inherited polyposis diseases or inflammatory bowel disease

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Hospital Universitario Rio Hortega Valladolid Valladolid Recruiting
Hospital Universitario Rio Hortega Valladolid Valladolid Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06314022 on ClinicalTrials.gov ↗ ← All trials in Spain