Clinical trial Recruiting at 1 site Interventional Ages 25 to 65

General practitioner outreach to boost cervical cancer screening participation

Official title: Intervention With General Practitioners to Improve Women's Participation in Cervical Cancer Screening

Run by Centre Hospitalier Intercommunal Creteil · NCT06527456 · Data updated 2026-11-12

This project will test whether outreach from a general practitioner (phone, SMS, or email) helps women aged 25–65 in Île‑de‑France who are overdue for cervical screening to book and attend screening.

Quick facts

Study typeInterventional
Ages25 Years to 65 Years
SexAll
Enrollment11200 (estimated)
SponsorCentre Hospitalier Intercommunal Creteil
Academic / other
Locations1 site (Créteil)
StatusRecruiting
StartedJanuary 21, 2026
Main results expectedAugust 2027
Study endsAugust 2027
Registry record updatedApril 14, 2026
Trial IDNCT06527456 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women aged 25 to 65 living in Île‑de‑France who are eligible for the DOCCU program, not up to date with cervical screening, and registered with a participating general practitioner in the UPEC CPTS area.

Probably not a fit

Patients who are already up to date with screening, have had a hysterectomy, are under active follow-up for cervical precancer or cancer, or explicitly refuse participation are unlikely to benefit from this outreach.

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

What this trial studies

This is a cluster-randomized trial that randomizes GP practices in the UPEC/Créteil area to either usual care or an intervention where the GP or their team contacts overdue patients by phone, SMS, email, or other means to encourage screening. Randomization at the practice level reduces contamination between clinicians in the same office. The main outcome is participation in the national organized screening program (DOCCU) among women not up to date with screening. Contact methods and timing are left to each GP’s discretion, and inclusion is limited to women aged 25–65 who are eligible for DOCCU and registered with participating GPs.

Why it matters

Potential benefit: If successful, the intervention could increase screening participation and lead to earlier detection and fewer advanced cervical cancers.

How similar studies have gone: Previous reminder and provider‑outreach studies have generally produced modest to moderate increases in screening uptake, so this intervention builds on established approaches.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Woman aged 25 to 65 living in Ile-De-France
* Eligible for DOCCU (not hysterectomized, not followed for a pre-cancerous or cancerous lesion of the cervix)
* Having declared the investigating general practitioner as a treating physician (MT) and whose MT practices in the territory of a CPTS in the UPEC area
* Affiliate to a social security scheme or beneficiary of such a scheme

Exclusion Criteria:

* Patient already included in a study on DOCCU
* Patient excluded from organized screening (cervical cancer, hysterectomy).
* Patient's opposition to participating in the study

Where it's running

  • Médecins généralistes dans le bassin de l'UPEC
    Créteil, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.