M.D. Anderson Cancer Center
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.
Cervical Cancer
HPV testing of women for cervical cancer screening
NA
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.
| Study Type : | INTERVENTIONAL |
| Estimated Enrollment : | 14600 participants |
| Masking : | NONE |
| Primary Purpose : | SCREENING |
| Official Title : | Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique |
| Actual Study Start Date : | 2020-12-22 |
| Estimated Primary Completion Date : | 2027-02-02 |
| Estimated Study Completion Date : | 2027-02-02 |
Information not available for Arms and Intervention/treatment
| Ages Eligible for Study: | 30 Years to 49 Years |
| Sexes Eligible for Study: | FEMALE |
| Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
RECRUITING
M D Anderson Cancer Center
Houston, Texas, United States, 77030