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.

Objectives:

The study objectives are outlined below:

1. To quantify the health impact of CCS&PT on the uptake of voluntary FP services.
2. To quantify the health impact of voluntary FP on the uptake of CCS&PT services.
3. To determine which promotional strategies are most effective to increase uptake of CCS&PT services.
4. To identify cost to deliver high quality CCS&PT services integrated into existing voluntary FP programs.
5. To determine client and provider acceptability of integrated CCS&PT and voluntary FP services using new screen and treat technologies.

Inclusion Criteria:

• 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.

Exclusion Criteria:

• Not meeting the inclusion criteria
• Physical or mental impairment that inhibits participation in the study
• Pregnant women