Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique

Running, not enrolling · Not applicable

Conditions studied: Cervical Cancer

In brief

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.

Key facts

Study ID

NCT05359016

Run by

M.D. Anderson Cancer Center

People needed

9014

Starts

2020-12-22

Expected to finish

2027-02-02

Last updated by the study team

2026-05-22

Who can join

Age: 30 and older, up to 49. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

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

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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