Skip to content

Acceptability of HPV-self Sampling

Evaluation of the Acceptability of HPV Self-sampling Among French Women Eligible for Cervical Cancer Screening

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03137563
Enrollment
356
Registered
2017-05-02
Start date
2017-05-15
Completion date
2019-07-30
Last updated
2020-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer

Keywords

Women, 25-65 years

Brief summary

This trial aimed at evaluating the acceptability of HPV self-sampling among french women eligible for cervical cancer screening (25 - 65 years old) in the region of Occitanie, in the south of France. Acceptability will be evaluated using an anonymous questionnaire and the main outcome of the study will be the response acceptability yes or no for HPV self-sampling. Secondary outcome will be analysis of socioeconomic determinants for the acceptability of HPV self-sampling. These data will help to propose new strategies for cervical cancer screening in France, particularly to taget non-attenting populations

Detailed description

Women will be recruted in 8 centers located in 2 departments , Aude and Herault (in the Region of Occitanie in the south of France).The questionnaire will be proposed to the women attending one of these eight centers by an investigator, who will verify the inclusion and exclusion criteria. The same person will collect the filled questionnaire. The questionnaire is anonymous and is composed of 15 questions evaluating the acceptability of HPV self-sampling and socio-economic determinants. These questionnaires will be collected and statistical analysis will be performed using appropriate tools. This study will bring informations on the acceptibility of HPV self sampling among french women eligible for cervical cancer screening in 2 Departements of the South of France. Self-sampling acceptability will be linked to socio-economic determinants. These data will be important to propose and evaluate new strategies to improve screening coverage, particularly of the context of the organized cervical cancer screening that will take place in France in 2018.

Interventions

OTHERquestionnaire

The questionnaire will be distributed and collected by the same investigator in one of the eight centers involved in the study. The investigator will verify the inclusion criteria and the absence of exclusion criteria.

Sponsors

Dépistages34 (Montpellier - France)
CollaboratorUNKNOWN
Adoc11 (Carcassonne - France)
CollaboratorUNKNOWN
Maison médicale Paul Valéry - Union Languedoc Mutualité - (Montpellier -France)
CollaboratorUNKNOWN
University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Women 25-65 years old * Living in the Aude or Herault departments * Informed patient

Exclusion criteria

* Virgins * Previous hysterectomy * Present or previous cervical pathology * Patient under guardianship or tutorship

Design outcomes

Primary

MeasureTime frameDescription
accept HPV self-sampling for cervical cancer1 dayResponse Yes or No to the question would you accept HPV self-sampling for cervical cancer screening ?

Secondary

MeasureTime frameDescription
Socioeconomic determinants of the response1 daySocioeconomic determinants of the response yes or no to the question would you accept HPV self-sampling for cervical cancer screening ?

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026