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Clinical Trials in Denmark / NCT07353632
Recruiting Observational

What Influence Re-participation in the Danish Colorectal Screening Program.

NCT07353632 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2024-09-23
Last updated
2026-01-20

Condition(s) studied

ColonoscopyScreening ColonscopyPain

Study summary

This prospective observational study investigates how participants experience screening colonoscopy within the Danish colorectal cancer screening program and how these experiences relate to clinical findings, procedural factors, and future participation in screening.

The study aims to evaluate patient-reported experiences such as pain, discomfort, preparation burden, emotional responses, and perceptions of healthcare staff, as well as staff-assessed pain during the procedure. These experiences will be examined in relation to colonoscopy findings, including polyp detection, histology, risk stratification, and colorectal cancer detection. In addition, procedure-specific variables such as insertion time, bowel preparation quality, completeness of colonoscopy, medication use, and adenoma detection rate will be analyzed in relation to patient experience.

A key focus is whether the experience of screening colonoscopy influences subsequent participation in the colorectal cancer screening program, particularly among individuals classified as low risk and re-invited for screening after two years. Registry-based follow-up will be used to assess re-participation.

Data are collected prospectively from two sources: (1) real-time procedure data entered by healthcare staff during colonoscopy and (2) patient-reported outcomes collected via a questionnaire completed shortly after the procedure. Additional outcome data are obtained from electronic medical records and national health and screening registries.

The study has no single predefined hypothesis. Instead, it serves as a data-generating platform designed to address both predefined and future research questions related to screening colonoscopy experiences, quality indicators, and screening adherence.

Eligibility

Sex
ALL
Min age
50 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adults undergoing screening-derived colonoscopy as part of the Danish colorectal cancer screening program * Written informed consent Exclusion Criteria: * Inability to understand or communicate in Danish * Lack of decision-making capacity, including cognitive impairment due to dementia or brain injury * Declines or withdraws informed consent

Primary outcome measure(s)

Trial sites (8)

FacilityCityRegionStatus
Sygehus Sønderjylland, University hospital of Southern Denmark Aabenraa Denmark Recruiting
Esbjerg Hospital, University Hospital of Southern Denmark Esbjerg Denmark Recruiting
Grindsted Sygehus Grindsted Denmark Recruiting
Regionshospitalet Gødstrup Gødstrup Denmark Recruiting
Holbæk Sygehus Holbæk Denmark Recruiting
Sjællands Universitetshospital Køge Køge Denmark Recruiting
Sjællands Universitetshospital, Nykøbing Nykøbing Falster Denmark Recruiting
Slagelse Sygehus Slagelse Denmark Recruiting

More Esbjerg Hospital - University Hospital of Southern Denmark trials in Denmark

Other trials for the same condition

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 NCT07353632 on ClinicalTrials.gov ↗ ← All trials in Denmark