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

NCT07438080 | Recruiting

• 2 other identifiers: 2023/CHU/372023-A02588-37
• Study Type: interventional
• Target: 300
• Locations: 1 country
• Sites: 2

Brief Summary

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

Conditions

HPV

Outcome Measures

Primary Outcomes (1)

• Rate of women who complete cervical cancer screening after the community health intervention,

  Rate of women aged 30 to 65 years living in vulnerable areas of Reunion Island who complete cervical cancer screening (HPV test or Pap smear) within 3months after the community health intervention, as documented in medical records or screening databases.

  3 months

Study Arms (1)

participant

EXPERIMENTAL

1. Awareness workshops on uterine cancer screening - small group workshops conducted in the form of discussion groups 2. Proposal for an HPV self-test (vaginal self-swab to detect high-risk HPV) as part of an individual consultation for participants whose CC screening is not up to date

Other: Public health workshop in community

Interventions

Public health workshop in community OTHER

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.

participant

Eligibility Criteria

• Age: 30 Years - 65 Years
• Gender Eligibility Details: people with uterus
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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

You may not qualify if:

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

Sponsors & Collaborators

• Centre Hospitalier Universitaire de la Réunion: lead

Study Sites (2)

Cegidd Saint Paul

Saint-Paul, France

RECRUITING

CegiDD Saint Pierre

Saint-Pierre, France

RECRUITING

MeSH Terms

Interventions

Residence Characteristics

Intervention Hierarchy (Ancestors)

Demography; Population Characteristics; Epidemiologic Measurements; Public Health; Environment and Public Health

Central Study Contacts

Emmanuelle THORE, dr

CONTACT

+262 262 74 23 80; direction@chor.re

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 7, 2025
• First Posted: February 27, 2026
• Study Start: April 9, 2025
• Primary Completion (Estimated): March 1, 2027
• Study Completion (Estimated): March 1, 2028
• Last Updated: February 27, 2026

Record last verified: 2025-08

Locations

FR (2)