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Recruiting NCT07438080

Concordance and Acceptability of Self-screening Compared to Screening Carried Out by a Health Professional for HPV, a Risk Factor for Anal Cancer, by Swab in People Living With HIV. A Randomized Controlled Crossover Study

No phase Interventional HPV

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: Public health workshop in community.
Who it may be relevant to
Registry conditions: HPV. 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 →

Overview

Comunity health actions are set up in populations of women aged 30 to 65 in vulnerable situations living in the outlying areas of Reunion Island. The idea is to evaluate those action on health

Interventions

  • Other Public health workshop in community
    1\) Cervical cancer screening awareness workshops, conducted in small groups through focus groups. -2) Proposal for an HPV self-test (vaginal self-swab to detect high-risk HPV) as part of an individual consultation for participants who are not up-to-date with their cervical cancer screening.

Primary outcome measures

  • Rate of women who complete cervical cancer screening after the community health intervention, [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Aged 30 to 65,
  • In a vulnerable situation (beneficiary of a state or departmental social service, or referred by a charity),
  • Resident in one of the two municipalities targeted by the study,
  • Supported by the social services of one of the two municipalities targeted by the study,
  • Having agreed to participate in sexual health awareness meetings organized on site

Exclusion criteria

  • Refusing to participate in the study
  • Having had a hysterectomy

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

Healthy volunteers: No

Study design

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

Study locations

France · 2 centers
  • Cegidd Saint Paul — Saint-Paul
  • CegiDD Saint Pierre — Saint-Pierre

Identifiers

NCT: NCT07438080 · 2023/CHU/37 · 2023-A02588-37

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗