ISRCTN39154605Completed未知
A pragmatic randomised controlled trial of response to an invitation to self-sampling for human papillomavirus (HPV) versus repeat invitation for cervical screening in persistent non-responders in Newcastle upon Tyne
Queen Mary University of London (UK)0 sites300 target enrollmentStarted: October 4, 2012Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 300
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- Female
Inclusion Criteria
- •Non-responders according to the North East Primary Care Services Agency (NEPCSA) recall process. They will have received their initial screening letter, plus a first reminder letter, plus at least two non-responder cards will have been sent to their General Practitioner, identified using the NEPCSA Exeter National Health Applications and Infrastructure Services (NHAISs) System.
Exclusion Criteria
- •1. Women who have written to the NEPCSA to document their refusal to take part in the NHSCSP
- •2. Women who contact the trial team and ask to be excluded from the trial
- •3. Pregnancy
- •4. Total abdominal hysterectomy
- •5. Never been sexually active
- •6. Women who are identified as becoming pregnant or undergoing hysterectomy following the initial test will be excluded from the analysis of data for secondary outcomes
- •7. HPV self-sample returned without a signed Informed Consent Form (ICF) (the Participant Information Leaflet (PIL) will state that samples returned without a signed consent form cannot be processed)
- •8. Informed Consent Form (ICF) returned with incomplete contact details whereby the test results cannot be sent
Investigators
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