Cervical cancer Cervical cancer
Conditions
Interventions
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: 1: Age 30 years or above 2: Non-compliant with cervical cancer population screening (‘non-attenders’) with an invitation during one, two or theoretically three rounds (‘un- or under screened’) 3: Informed consent.
Exclusion criteria
Exclusion criteria: 1: Age <30 years 2: Attending cervical cancer population screening according to invitation 3: Recent (< 1 year) cervical PAP smear for other indication Midwives who participate in the study are also asked to guard logbook information and join focus groups. For this group, the only inclusion criterium is that the e-learning is successfully completed in advance.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measure screening participation among postpartum women by comparing those who received counselling with those who did not.Assess long-term effectiveness, cost-effectiveness, and feasibility of the counselling programme.Evaluate the impact of counselling on:Informed decision-makingScreening outcomes | — |
Secondary
| Measure | Time frame |
|---|---|
| Identify factors affecting compliance or non-compliance with colposcopy or follow-up care after an HPV-positive result.Track CIN2+ detection after participation.Evaluate barriers and feasibility of implementing the programme, including obstacles to participation.Assess the long-term impact of counselling on future screening attendance.Examine the programme's impact on cervical cancer incidence and mortality in the coming decades. | — |
Countries
Netherlands
Contacts
Public ContactR.L.O. Laar
Erasmus MC, Universitair Medisch Centrum Rotterdam
Outcome results
None listed