Actively Recruiting

Phase Not Applicable
Age: 50Years - 69Years
All Genders
Healthy Volunteers
ID06696534

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

Led by ADVANCED MARKER DISCOVERY S.L. · Updated on 2025-10-02

1000

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

Sponsors

A

ADVANCED MARKER DISCOVERY S.L.

Lead Sponsor

S

SERMAS

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying how participants feel about and prefer different screening methods in a colorectal cancer screening program. This low-risk interventional study focuses on adults aged 50 to 69 years who are asymptomatic and part of a population-based screening program. The main goal is to understand participants' experiences and preferences after undergoing fecal occult blood test (FOBT) screening. Participants will complete two questionnaires: one about their preference for colorectal cancer screening methods and another about their experience in the screening program. These surveys will be conducted within the colorectal cancer screening program involving average-risk individuals undergoing fecal immunochemical test (FIT) or FOBT. During the study, participants will provide information through these questionnaires, and their clinical data will be shared with investigators or health personnel. The primary outcome is the value of the questionnaires related to the screening program, assessed over 12 months. Participants will be monitored for their responses and experiences during this period, with no additional interventions or treatments involved.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 50Years - 69Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants ages from 50 to 69 years at the time of informed consent.
  • Participants invited to take part in a population-based colorectal cancer screening program eligible for FOBT at the Primary Health Care Center.
  • Participants must sign informed consent after understanding the study's nature and risks.
Not Eligible

You will not qualify if you...

  • Participants who have not delivered a stool sample at the Primary Health Care Center before signing informed consent.
  • Participants with a previous colonoscopy following a positive FOBT result.
  • Participants in a dependent personal or non-medical relationship with the study sponsor or investigators.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - 12 months

Participants complete questionnaires to share their preferences and experiences regarding colorectal cancer screening methods.

1 to 2 visits depending on questionnaire completion

Trial Site Locations

Total: 2 locations

1

UCSP Sete Rios

Lisbon, Portugal

Not Yet Recruiting

2

CS Mar Báltico

Madrid, Madrid, Spain

Actively Recruiting

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Research Team

M

Marta Jimenez, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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Frequently Asked Questions

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Published Research Related To This Trial

Improving compliance to colorectal cancer screening using blood and stool based tests in patients refusing screening colonoscopy in Germany.

Andreas Adler, Sebastian Geiger, Anne Keil...

https://pubmed.ncbi.nlm.nih.gov/25326034

Complete cancer prevalence in Europe in 2020 by disease duration and country (EUROCARE-6): a population-based study.

Roberta De Angelis, Elena Demuru, Paolo Baili...

https://pubmed.ncbi.nlm.nih.gov/38307102