Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique
Interventionnel
Phase non listée
M D Anderson Cancer Center
Sponsor: M.D. Anderson Cancer Center
Dernière synchronisation : 4 novembre 2025 Avis - Les informations proviennent de registres publics et peuvent ne pas refléter les changements en temps réel sur le site local.
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
Critères d'exclusion
Aucun
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Détails de la conception
AllocationN/A
Modèle d'interventionSingle Group Assignment
MasquageNone (Open Label)
Nombre à inscrire14600
Bras et interventions
Bras
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
Mesures des résultats
Mesures des résultats primaires
Number of women who will undergo Cervical Cancer Screening by HPV testingthrough study completion, an average of 1 year
Mesures des résultats secondaires
Aucun
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