Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique
Interventional
Phase not listed
M D Anderson Cancer Center
Sponsor: M.D. Anderson Cancer Center
Last Updated: November 4, 2025 Notice- Information is sourced from public registries and may not reflect real-time changes at the local site.
The goal of this operational research study is to develop, implement and test integrated CCS&PT and voluntary FP service delivery models to evaluate whether integrated service delivery can optimize uptake and health impact of both services. The study objectives and learning questions are listed below, along with key outcomes that will be measured.
* Women 30 - 49 years or all women living with HIV
* Not currently pregnant
* Patients with a cervix (women who have undergone a total hysterectomy with removal of the cervix are not eligible)
* Living in Maputo or Gaza
* Willing and able to provide informed consent for services.
* Physical or mental impairment that inhibits participation in the study
* Pregnant women
Exclusion Criteria
None
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Design Details
AllocationN/A
Intervention ModelSingle Group Assignment
MaskingNone (Open Label)
Number to Enroll14600
Arms & Interventions
Arms
Interventions
Type: Experimental
Description: Women enrolled in this study will receive HPV testing for cervical cancer screening. They will be offered self-sampling. And also they will be offered voluntary Family Planning services, as appropriate.
Interventions:
HPV testing of women for cervical cancer screening
Outcome Measures
Primary Outcome Measures
Number of women who will undergo Cervical Cancer Screening by HPV testingthrough study completion, an average of 1 year