Human Papillomavirus (HPV) testing on self-collected samples to increase uptake of cervical screening in non-attenders
Not Applicable
Completed
- Conditions
- Topic: Primary Care Research Network for EnglandSubtopic: Not AssignedDisease: All DiseasesInfections and Infestations
- Registration Number
- ISRCTN35286331
- Lead Sponsor
- Queen Mary University of London (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Women aged 28-64 years who are eligible for cervical screening and are at least 6 months overdue (i.e. no cervical cytology recorded in the GP records in the past 3.5 years if aged 28-49 or 5.5 years if aged women 50-64)
Exclusion Criteria
1. Women unable to provide informed consent (e.g. because of learning difficulties)
2. Women whose command of English is not sufficient to obtain informed consent
3. Women in whom cervical screening is inappropriate, for example because they are pregnant or terminally ill
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of women who return a self-collected sample for HPV testing measured at the end of the study
- Secondary Outcome Measures
Name Time Method 1. Proportion of women who are found to have cervical intraepithelial neoplasia; Timepoint(s): End of study<br>2. Proportion of women who are found to test HPV positive; Timepoint(s): End of study