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Evaluating the Impact of Different Methods of HPV DNA Testing for Cervical Cancer Screening in Primary Care Settings

RecruitingNAAges 30 Years - 69 YearsFemaleNational Healthcare Group Polyclinics
NCT06528184 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Primary objective of the study is to determine the extent that offering of self-sampling in addition to clinician-sampling Human Papillomavirus (HPV) DNA testing will increase detection of HPV DNA through an increase in uptake rates of cervical cancer screening as compared to offering clinician-sampling HPV DNA testing alone. The hypothesis is that offering additional self-sampling will increase the detection of high-risk HPV DNA by at least 7.7%.

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📋 Eligibility rules (as published)
Inclusion Criteria: * 30-69 years old female Singapore citizens * Due for cervical cancer screening * Engaged in sexual intercourse before * Able to give informed consent * Able to read and communicate in English, Chinese or Malay Exclusion Criteria: * Virgo intacta * Pregnancy * History of cervical cancer, precancerous cervical lesions and total hysterectomy
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What it tests

  • Self-sampled HPV DNA testing
  • Clinician-sampled HPV DNA test
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Where

1 site
National Healthcare Group Polyclinics
Singapore, Singapore
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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