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Human Papillomavirus (HPV) testing on self-collected samples to increase uptake of cervical screening in non-attenders

Human Papillomavirus (HPV) testing on self-collected samples to increase uptake of cervical screening in non-attenders: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35286331
Enrollment
200
Registered
2013-11-21
Start date
2013-12-22
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Topic: Primary Care Research Network for England

Interventions

Women aged 28-64 who are at least 6 months overdue their smear will be flagged in the EMIS electronic patient record system at GP surgeries. GPs, nurses and healthcare practitioners will be asked to o

Sponsors

Queen Mary University of London (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Proportion of women who return a self-collected sample for HPV testing measured at the end of the study

Secondary

MeasureTime frame
1. Proportion of women who are found to have cervical intraepithelial neoplasia; Timepoint(s): End of study 2. Proportion of women who are found to test HPV positive; Timepoint(s): End of study

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026