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Taking people in FranceNo phase

Tests an AI chatbot to help women join cervical cancer screening

Tests an AI chatbot decision aid for women aged 30 to 65 offered HPV self-sampling.

Plain-language title generated from the registry record
Registry title: Using Artificial Intelligence-based ChatBot to Improve Women's Participation to Cervical Cancer Screening Programme

Key facts

Where
Carcassone, FranceSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 30 and 65 years old?

Source: NCT05286034, who can take part

Where in France

  • Centre Régional de Coordination des Dépistages des Cancers-Centre d'OccitanieCarcassone, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
International Agency for Research on Cancer
Trial code
NCT05286034
Record updated
27 March 2026
Original description
This project looks to improve the return rate of HPV self-sampling (HPVss) as well as the management of women HPVss positive.Read full original descriptionShow less

Artificial Intelligence-assisted Decision-making to Improve Women's Participation to Cervical Cancer Screening in Occitanie Region-France

This project looks to improve the return rate of HPV self-sampling (HPVss) as well as the management of women HPVss positive.

Inclusion: aged 30-65; did not perform a pap smear in the last 4 years; are living in deprived clusters in the Occitanie region; did not answer to a first "invitation" letter to perform a clinician-collected HPV testing.

Exclusion: outside the target age group; had a Pap smear in the past 3 years; had hysterectomy including cervix; are pregnant; already scheduled a screening appointment or had just attended a HPV screening; had a cervical abnormality that was under exploration and/or treatment; participated to the study pilot.

ClinicalTrials.gov NCT05286034