Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 30
Maximum Age: 49
Healthy Volunteers: f
View:
• 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.
Locations
United States
Texas
M D Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Mila Salecedo, MD, PHD
mpsalcedo@mdanderson.org
832-696-6794
Time Frame
Start Date: 2020-12-22
Estimated Completion Date: 2027-02-02
Participants
Target number of participants: 14600
Treatments
Experimental: HPV testing of women for cervical cancer screening
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.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center
Collaborators: William Marsh Rice University, Population Services International, Eduardo Mondlane University