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Using Artificial Intelligence-based ChatBot to Improve Women's Participation to Cervical Cancer Screening Programme (AppDate-You)

I

International Agency for Research on Cancer

Status

Begins enrollment in 1 month

Conditions

Cervical Cancer Screening
Cervical Cancer

Treatments

Behavioral: Decision aid tailored to women with lower educational attainment,accessible via artificial intelligence-based Chatbot platforms

Study type

Interventional

Funder types

Other

Identifiers

NCT05286034
IEC 21-16

Details and patient eligibility

About

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

Full description

France has already implemented a cervical screening programme based on HPV test for the whole female population aged 30-65 years. Non-participant women can perform HPV test at their home. However, less than 20% of French women performed vaginal self-sampling when a kit was sent to their home. Women with lower income and educational levels participate less to cervical screening. A variety of personal, practitioner, test-related and logistical barriers negatively impact the screening participation of French women. Key barriers to participation could be addressed by overcoming disparities in HPV-related knowledge and perceptions about cervical cancer screening. This study aims to evaluate the impact of sending HPV self-sampling kit at women's home, associated with providing, through multiple mobile channels, a multi-language decision aid designed for women with lower education accessible via artificial intelligence-based ChatBot. This decision aid will help women review high quality evidence on cervical cancer disease and screening modalities.

Enrollment

3,000 estimated patients

Sex

Female

Ages

30 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria: eligible women will be:

  • 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 criteria: ineligible women will be those:

  • 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

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,000 participants in 2 patient groups

Intervention group
Experimental group
Description:
Women randomized to this group will be sent screening reminder letters to perform HPV self-sampling test, with access to a decision aid tool tailored to those with low education levels. This tool will be available via Chatbot platforms.
Treatment:
Behavioral: Decision aid tailored to women with lower educational attainment,accessible via artificial intelligence-based Chatbot platforms
Control group
No Intervention group
Description:
Women randomized to this group will be sent screening reminder letters to perform HPV self-sampling test (Standard care)

Trial contacts and locations

1

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Central trial contact

Farida Selmouni, Dr

Data sourced from clinicaltrials.gov

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