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Not yet recruiting NCT06656611

Mobile Outreach Screening of High-Risk Human Papillomavirus Infection in Women with Limited Access to Health Services in Seine-Saint-Denis (greater Paris Area, France)

No phase Interventional Women's Health: Cervical Neoplasm

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: HPV self sampling.
Who it may be relevant to
Registry conditions: Women's Health: Cervical Neoplasm. Basic parameters: 30 years — 65 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

PAPMOBILE: Mobile Outreach Screening of High-Risk Human Papillomavirus Infection in Women with Limited Access to Health Services in Seine-Saint-Denis (greater Paris Area, France)

Overview

The study is a prospective cervical cancer screening intervention in the nonclinical setting of a mobile testing unit in a vehicle, using point-of-care HPV PCR tests with self-collected vaginal swabs. It is designed for women with limited access to healthcare and prevention in underprivileged municipalities in the greater Paris area (Seine-Saint-Denis department, detailed in Annexe 3). HPV positive participants will receive counseiling and guidance to help them find a healthcare professional to take care of their needs

Interventions

  • Other HPV self sampling
    Selected women will perform a vaginal self-sampling using a swab

Primary outcome measures

  • Total number and proportion of eligible women (age 30 to 65, unscreened for cervical cancer for 3 to 5 years) who had an HPV PCR test on a self-collected vaginal sample when offered in a nonclinical setting by the Bus Santé de Seine-Saint-Denis [Time frame: Day 0]
Secondary outcome measures (12)
  • Declined to participate: number and why [Time frame: Day 0]
  • Description of the barriers to cervical cancer screening in the target population [Time frame: Day 0]
  • Proportion of complete HPV-HR PCRs run onboard the Bus and proportion with same-day results available to the participants [Time frame: Day 0]
  • Frequency of positive HPV-HR tests and of invalid HPV-HR tests using SCVS samples [Time frame: Day 0]
  • Description of HPV types in the participant population [Time frame: Day 0]
  • Comparison of HPV-HR negative and HPV-HR positive participants [Time frame: Day 0]
  • Proportion of secondary pelvic examination and cervical PAP smears in HPV-positive participants ; in Step 1 (laboratory-based PCR) and Step 2 (PCR aboard the Bus with same-day results) [Time frame: Day 0]
  • Proportion of Chlamydiae trachomatis and Neisseria gonorrhoea STIs [Time frame: Day 0]
  • Number and frequency of cytological abnormalities and cervical lesions in participants who had a PAP smear following a positive HPV-HR test ; in Step 1 (laboratory-based PCR) and Step 2 (PCR aboard the Bus with same-day results) [Time frame: Day 0]
  • Proportion of valid self-collected vaginal swabs (cellular density, valid HPV PCR) [Time frame: Day 0]
  • Unavailability of point-of-care HPV-HR PCR: number of days and why (reagent shortage, instrument of power failure, environmental conditions, short-staffing…) [Time frame: Day 0]
  • Reliability of vaginal self-sampling in a nonclinical setting: proportion of valid samples, types of non-conformity [Time frame: Day 0]

Eligibility criteria

Inclusion criteria

  • \- Women from 30 to 65 years of age presenting to the " Bus Santé " nonclinical testing unit, eligible to cervical cancer screening by an HPV-HR test
  • Women affiliated to the French social security or immigrants benefiting from the state medical aid program for undocumented immigrants (Aide Médicale d'Etat). The inclusion of people not affiliated to a social security system is an exception and depends on the decision of the Personal Protection Committee, if it is based on an expected benefit for these people of a nature to justify the foreseeable risk incurred.
  • The intervention is designed for vulnerable women with limited access to healthcare, including but not limited to:
  • Women living in shelters and hostels, women living in the streets, in squats, hot-bedding arrangements, emergency social housing;
  • Recent immigrants, documented or undocumented;
  • Young adults from priority neighbourhoods,
  • Isolated or marginalized women
  • Free, informed, written consent, signed by the person and the investigator at the latest on the day of inclusion and before any sampling carried out as part of the trial (article L1122-1-1 of the Public Health Code)

The Bus will operate in underprivileged neighbourhoods in the greater Paris area (eastern Seine-Saint-Denis department.

Exclusion criteria

  • Screened for cervical cancer by a PAP smear in the last 3 years or by an HPV test in the last 5 years,
  • Women on their period (haemoglobin inhibits PCRs)
  • Pregnancy in the 2nd and 3rd trimesters
  • Total hysterectomy; absence of a vagina
  • Women under guardianship/tutelage

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Screening

Study locations

France · 1 center
  • Hopital Avicenne — Bobigny

Publications

  • Rahib D. Place de l'auto-prélèvement " à domicile " dans les stratégies de dépistage du VIH et des autres infections sexuellement transmissibles chez les hommes ayant des relations sexuelles avec des hommes en France. 2022; Available at: https://theses.fr/api/v1/document/2022SORUS219
  • Reques L, Rolland C, Lallemand A, Lahmidi N, Aranda-Fernandez E, Lazzarino A, Bottero J, Hamers F, Bergeron C, Haguenoer K, Launoy G, Luhmann N. Comparison of cervical cancer screening by self-sampling papillomavirus test versus pap-smear in underprivileged women in France. BMC Womens Health. 2021 May 26;21(1):221. doi: 10.1186/s12905-021-01356-8. PMID 34039341
  • Pretsch PK, Spees LP, Brewer NT, Hudgens MG, Sanusi B, Rohner E, Miller E, Jackson SL, Barclay L, Carter A, Wheeler SB, Smith JS. Effect of HPV self-collection kits on cervical cancer screening uptake among under-screened women from low-income US backgrounds (MBMT-3): a phase 3, open-label, randomised controlled trial. Lancet Public Health. 2023 Jun;8(6):e411-e421. doi: 10.1016/S2468-2667(23)00076 PMID 37182529
  • CNR HPV. Trousses de détection des HPV ayant bénéficié d'une validation clinique pour le dépistage du cancer du col de l'utérus. 2023; Available at: https://cnr-hpv.fr/wp-content/uploads/2023/03/Liste-des-trousses-de-detection-et-de-genotypage-des-HPV-validees-par-les-fabricants-de-milieux-v11.pdf.
  • Institut National du Cancer, CNR HPV, France. Référentiel national - Dépistage du cancer du col de l'utérus - cadre et modalités de recours aux autoprélèvements vaginaux. 2022; Available at: https://www.e-cancer.fr/Expertises-et-publications/Catalogue-des-publications/Referentiel-national-Depistage-du-cancer-du-col-de-l-uterus-cadre-et-modalites-de-recours-aux-autoprelevements-vaginaux.
  • Dourgnon P, Jusot F, Sermet C, Silva J. La santé perçue des immigrés en France. 2008; Available at: https://www.irdes.fr/Publications/Qes/Qes133.pdf.

Identifiers

NCT: NCT06656611 · IMEA 072

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗