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Interventions to increase participation in the cervical cancer screening program for non- attendees in Sweden

Participation in interventions and recommended follow-up for non-attendees in cervical cancer screening- taking the women's own preferred test method into account - a Swedish randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN78719765
Enrollment
10614
Registered
2020-01-23
Start date
2016-04-01
Completion date
Unknown
Last updated
2020-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical cancer and cervix dysplasia Cancer

Interventions

Non-attendees are defined as women who had not participated in the cervical cancer screening programme during the last six years if aged 30 - 49, and the last eight years if aged 50 - 64. This strateg

Sponsors

Linköping University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Non- attendees (defined as women who had not participated in the cervical cancer screening programme during the last six years if aged 30-49 and the last eight years if aged 50-64)

Exclusion criteria

Exclusion criteria: All women 30-64 years old that had participated after the last invitation as recommended in the cervical cancer screening program

Design outcomes

Primary

MeasureTime frame
Participation rate measured using patient records at six months after invitations were sent

Secondary

MeasureTime frame
1. Choice of intervention measured using patient records at the end of the study 2. Cytological diagnoses found in the index Pap smear at the time of analysis

Countries

Sweden

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026