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NCT06640075Active, not recruiting

Community Co-produced Action for Improved Access to Cervical Cancer Screening in Cameroon

Co-produced Community Action for Improved Access to Cervical Cancer Screening (Act4CC): a Mixed-methods Study in Rural Areas of the Mifi Health District

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

Background - The burden of cervical cancer is unequally distributed globally, with over 90% of deaths occurring in low- and middle-income countries (LMICs), mainly due to insufficient uptake of preventive measures such as screening. In 2020, the World Health Organization launched a global initiative for the worldwide elimination of cervical cancer as a public health issue, setting a target of 70% of women screened with a high-performance test. In Cameroon, this target is far from being reached, and rural communities are disproportionately affected by low uptake of screening services. Recently, a new cervical cancer screening program has launched in the Bafoussam Regional Hospital, in the capital of the Mifi Health District, as part of a larger research project. To develop a context-specific strategy improving access to screening for women living in rural areas of the district, the active participation of community members for the co-development and implementation of local strategies for cervical cancer screening may be key to improving population screening coverage. Objective - The aim of this study is to evaluate the use of community co-produced action (CCA) for the development and implementation of HPV-based cervical cancer screening strategies compared to a traditional hospital-based approach in rural areas of the Mifi Health District in Cameroon. Methods - Using a cluster-randomized study design, participatory workshops with community members will be led in 7 rural health areas assigned to the intervention arm, with the aim of codeveloping local strategies for HPV-based cervical cancer screening adapted to the setting. The co-produced strategies may include raising awareness among eligible women (aged 30-49 years, or 25-49 years if HIV-positive), as well as facilitating access to screening tests, results and follow-up. Women living in one of the 7 health areas assigned to the control arm will be invited by community health workers to undergo screening at the Bafoussam Regional Hospital. In both study arms, screened women will be included in the GENOVA study, a cervical cancer screening trial offering free-of- charge HPV testing followed by triage by visual inspection or genotyping for HPV-positive women, and free treatment according to triage results. CCA will be evaluated by assessing its effectiveness for screening uptake. Screening coverage among eligible women will be estimated during one year after implementation of screening strategies in both study arms, based on population statistics provided by the Mifi health district for each health area. Expected results - Developing context-sensitive solutions to cervical cancer screening through a community-based participatory approach in rural areas of the Mifi health district is expected to improve screening participation rate.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
800 (estimated)
First submitted
10 Oct 2024
Start date
13 Apr 2024
Primary completion date
21 May 2026
Lead sponsor
Prof. Patrick Petignat
NCT number
NCT06640075

What you commit to

  • Study type: Interventional
  • Planned participants: 800
  • From 13 Apr 2024 to the primary completion date, 21 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • previous hysterectomy

Other illness

  • known cervical cancer
  • symptoms compatible with cervical cancer
  • terminal disease other than cervical cancer
  • cervical cancer screening test in the last 5 years (3 years if HIV-positive)

Other

  • pregnancy at the time of screening
  • lack of discernment capacity

Who the study is looking for

  • Women aged 30-49 years old (25-49 years old if HIV-positive)
  • Residency in one of the 14 rural health areas of Mifi health district
  • Ability to give signed informed consent

Age in the registry: 25 years to 49 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bafoussam Regional Hospital
Coordinator of this site? Confirm its status
BafoussamCameroonUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.