Cervical cancer Cancer Malignant neoplasm of cervix uteri
Conditions
Interventions
1. Pre-leaflet arm (Phase 1) - Surgeries will be cluster randomised with women either receiving the pre-leaflet in combination with a standard invitation letter or the standard invitation letter alone
Sponsors
University of Manchester (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women aged 25 in Manchester and 20 in Aberdeen who are due to receive their first invitation for cervical screening
Exclusion criteria
Exclusion criteria: 1. Women who are not aged 25 (20 in Aberdeen) and receiving their first invitation for screening will not be eligible to participate 2. Women who are pregnant 3. Women who do not have a cervix 4. Women who have made an informed decision not to participate in the cervical screening programme
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The uptake of cervical screening: 1.1. In response to the pre-leaflet (phase 1) 1.2. In response to the offer of each of the interventions (nurse navigator, self-sampling, timed appointments) (phase 2) 2. The uptake of internet booking (phase 1) Measured at 3, 12 and 30 months after the date the woman become eligible for cervical screening (i.e. her 25th or 20th birthday). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The differences between outcomes in Aberdeen between vaccinated and unvaccinated women 2. The differences between Aberdeen and Manchester 3. Cost-effectiveness of the interventions, individually and as packages of interventions | — |
Countries
England, United Kingdom
Outcome results
None listed