Clinical trial · Interventional
Evaluating Innovative Technologies and Approaches to Addressing Cervical Cancer in Gaza and Maputo Cidade Provinces in Mozambique
NCT05359016CI-TRIAL-00112414active not recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| HPV testing of women for cervical cancer screening | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- HPV testing of women for cervical cancer screening
- 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.
- interventionNames
- Behavioral: HPV testing of women for cervical cancer screening
Primary outcomes (1)
- measure
- Number of women who will undergo Cervical Cancer Screening by HPV testing
- timeFrame
- through study completion, an average of 1 year
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 30 Years
- Maximum age
- 49 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.