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Clinical Trials in Portugal / NCT06696534
Recruiting Not applicable

Exploring Participant Preference for Screening Methods and Experience Into Colorectal Cancer Screening Programme

NCT06696534 · tracked via the Priya Life Science Portugal tracker
Phase
Not applicable
Started
2025-05-19
Last updated
2025-10-02

Condition(s) studied

Screening for Colon CancerSurvey and Questionnaire

Investigational drug(s) / intervention(s)

Survey using a questionnaire.Survey using a questionnaire.

Survey using a questionnaire.: Preference questionnaire for colorectal cancer screening methods

Survey using a questionnaire.: Experience questionnaire into colorectal cancer screening programme

Study summary

The goal of this low-risk interventional study is to analyze participants' assessment of colorectal cancer screening program through screening method preference and experience after FOBT analysis in screaned participant population for colorectal cancer; could include any of the following: both sexes, age 50-69 years, asympthomatic volunteers. The main aims to answer are:

* Values of experience of participants into screening programme.
* Values of preferences of participants for screening methods.

Participants will answer two questionnaires and they'll be given their information and clinical data to investigator or health personnel.

Eligibility

Sex
ALL
Min age
50 Years
Max age
69 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Participants ages from 50 to 69 years (both included) at the time of informed consent signed. * Participants invited to participate in population-based screening programme who are eligible to undertake FOBT at the Primary Health Care Center. * Participants should sign an informed consent. They must understand the nature, significance, implications, and risks of the clinical study before signing the informed consent form. Exclusion Criteria: * Participants who have not delivery a stool sample in the Primary Health Care Center before signing the informed consent form. * Participants with a previous colonoscopy in consequence of a FOBT positive result. * Participants who are in a dependent personal or non-medical relationship with the Sponsor or the Investigators.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
UCSP Sete Rios Lisbon Portugal Not Yet Recruiting
CS Mar Báltico Madrid Madrid 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 NCT06696534 on ClinicalTrials.gov ↗ ← All trials in Portugal