Clinical trial Recruiting at 1 site Interventional Ages 50 to 69

Text reminders to boost colorectal cancer screening participation

Official title: Impact of SMS Notifications on the Colorectal Cancer Screening Program

Run by Corporacion Parc Tauli · NCT07628998 · Data updated 2026-11-12

A large group of people aged 50–69 in Vallès Occidental will be randomised to receive a reminder text message five weeks after an initial invitation, to see if it increases uptake of the FIT screening compared with the standard postal letter.

Quick facts

Study typeInterventional
Ages50 Years to 69 Years
SexAll
Enrollment10084 (estimated)
SponsorCorporacion Parc Tauli
Academic / other
Locations1 site (Sabadell, Catalonia)
StatusRecruiting
StartedMay 5, 2026
Main results expectedSeptember 2026
Study endsDecember 2026
Registry record updatedJune 22, 2026
Trial IDNCT07628998 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 50–69 who have not participated in the screening within 5 weeks of invitation and reside in Vallès Occidental.

Probably not a fit

Individuals who have already participated, those ineligible due to exclusion criteria, or those who do not respond to text messages may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pragmatic randomized trial tests whether a single SMS reminder can increase participation in a population-based colorectal cancer screening program using fecal immunochemical testing. Participants are adults 50–69 who have not completed screening five weeks after the initial invitation and are randomized 1:1 to receive an SMS reminder or continue with the standard postal reminder. The study leverages the Alhora secure messaging system and integrates with existing screening workflows in Vallès Occidental, with outcomes analyzed by intention-to-treat and per-protocol. A qualitative pilot informed the SMS content to ensure readability and cultural appropriateness. Results will inform whether mobile reminders can shorten response times and raise overall participation in screening efforts.

Why it matters

Potential benefit: If successful, the approach could substantially raise screening participation, potentially leading to earlier detection of colorectal neoplasms.

How similar studies have gone: Previous pilots and related public health reminders have shown promise for increasing uptake, but results can vary by setting and population.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Women and men aged 50 to 69 years.
* Residents of the Vallès Occidental area.
* Individuals invited to the Colorectal Cancer Screening Program (PDPCCR) who have not participated within 5 weeks of the initial invitation.

Exclusion Criteria:

* Personal history of colorectal cancer.
* Inflammatory bowel disease (IBD)
* Colorectal polyps requiring specific clinical follow-up.
* Hereditary polyposis syndromes.
* High-risk family history of colorectal cancer: a first-degree relative diagnosed before age 50, or two or more first-degree relatives at any age.
* Severe morbidity that precludes the performance of a colonoscopy in the event of a positive test result.

Where it's running

  • Unitat de Cribratge de Cáncer, Consorci Corporació Sanitaria Parc Taulí
    Sabadell, Catalonia, Spain
    Recruiting

Study contacts

  • Principal investigator: Anna Selva Olid, PhD, MPH, MD — Corporación Parc Taulí
  • Study coordinator: Anna Selva Olid, PhD
  • Email: aselva@tauli.cat
  • Phone: +34937231010

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.