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Completed

NCT Number: NCT03137563

Acceptability of HPV-self Sampling

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

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Questionnaire

Other

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.

Other names: Distribution of an anonymous questionnaire

Primary outcomes

  1. accept HPV self-sampling for cervical cancer

    Time frame: 1 day

    Response " Yes " or " No " to the question " would you accept HPV self-sampling for cervical cancer screening ?

Secondary outcomes

  1. Socioeconomic determinants of the response

    Time frame: 1 day

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

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Collaborators

  • Adoc11 (Carcassonne - France)
  • Dépistages34 (Montpellier - France)
  • Maison médicale Paul Valéry - Union Languedoc Mutualité - (Montpellier -France)

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2017
Study completion
2019
First posted
May 2, 2017
Registry last updated
Dec 31, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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