UNC Project-Malawi
Lilongwe, Malawi
NCT Number: NCT04286243
The purpose of the study is to determine the acceptability, appropriateness, and feasibility of implementing new strategies to screen and treat eligible women for cervical cancer through a cluster randomized trial of two different models. Both models offer the same screening and treatment algorithm, but one will be based in Voluntary Family Planning (VFP) or other clinics and the second will be based in the community. Participants will be recruited from two districts in Malawi with the highest HIV prevalence in the country: Lilongwe in the Central Region and Zomba in the Southern Region.
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Notify Me15 year–50 year
Female
Interventional
Not applicable
Lilongwe, Malawi
Cervical cancer is largely preventable through screening and preventive therapy. This is a cluster randomized trial that will integrate a novel cervical cancer screen-and-treat algorithm into voluntary family planning (VFP) services via two different models aimed at reducing barriers to screening and treatment in resource limited settings. Model 1 involves: 1) cervico-vaginal self-sampling for high-risk HPV (hr-HPV) while waiting for appointments at the VFP clinic or other clinics, 2) same-day visual inspection with acetic acid (VIA) for those women found to be hr-HPV-positive by rapid GeneXpert HPV testing, and 3) same-day thermocoagulation treatment for HPV-positive women who are eligible for ablative therapy by VIA. Model 2 will offer women the same services as in Model 1, but they will also be given the option to perform cervico-vaginal self-sampling in the community via Heath Surveillance Assistants (HSAs) who will bring their HPV sample to the clinic and notify them to return to the clinic for VIA and possible same-day thermocoagulation if their hr-HPV test is positive. Participants will be recruited from 16 high HIV-prevalence clinics in either Lilongwe in the Central Region or Zomba in the Southern Region. The broad objective of the project is to compare the effectiveness and budget impact of these two models for averting potential cervical cancer cases and to evaluate the implementation and acceptability of the models in multiple different health care facility settings.
A systematic Implementation Evaluation will be conducted throughout implementation of the assigned models at the study health facilities to determine the success/failure in the delivery of intervention packages. The study team will employ the following mixed method data collection assessments:
Finally, an Endline Household Survey will be completed among a random sample of women selected from all of the facilities' catchment areas (N= approximately 8,000). This survey will ask questions about basic demographic information, reproductive health information, HIV status, distance to the nearest health facility, prior VFP use, VFP use during project implementation, prior cervical cancer screening and preventive therapy (CCSPT) services received, and any CCSPT services received during project implementation.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Health care providers In-Depth Interviews (IDIs) and Focus Group Discussions:
Client In-Depth Interviews:
Client Exit Surveys:
Endline Household survey:
Exclusion criteria
Endline Household survey:
Offering HPV self-collection for cervical cancer screening in the community
Offering HPV self-collection for cervical cancer screening in the clinic
Time frame: 12 months after model implementation
Effectiveness of community-based cervical cancer screening as measured through Endline Household Surveys
Time frame: 12 months after model implementation
Effectiveness of integrating community-based cervical cancer screening into family planning services as measured through Endline Household Surveys
Time frame: 12 months after model implementation
Acceptability and feasibility of service provision as measured through routine assessments
Time frame: 12 months after model implementation
Acceptability and feasibility of service provision as measured through routine assessments
Time frame: 12 months after model implementation
Acceptability and feasibility of cervical cancer screening and preventive therapy as measured through client exit surveys
Time frame: 12 months after model implementation
Acceptability of family planning services as measured through client exit surveys
Time frame: 12 months after model implementation
The cost per client of adding cervical cancer screening and preventive therapy to voluntary family planning services in each model as measured through routine assessments and client exit surveys
University of North Carolina, Chapel Hill
Other
UNCPM 21904 - Prevention of Cervical Cancer Through an HPV-based Screen-and-treat Strategy in Malawi: a Cluster Randomized Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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