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Self-Sampling in Women Who Do Not Undergo Routine Cervical Screening

The Potential Role of Self-sampling in Women Who do Not Attend for Cervical Screening - a Randomised Controlled Trial

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00977392
Enrollment
3000
Registered
2009-09-15
Start date
2009-06-30
Completion date
2011-03-31
Last updated
2013-08-07

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

Conditions

Health Status Unknown, Precancerous Condition

Keywords

human papilloma virus infection, health status unknown

Brief summary

RATIONALE: Women who do not undergo routine cervical screening may be more likely to collect a self-sample for human papillomavirus testing. PURPOSE: This randomized clinical trial is studying self-sampling in women who do not undergo routine cervical screening.

Detailed description

OBJECTIVES: * To ascertain whether women who do not attend for cervical screening are more likely to respond to the opportunity to collect a self-sample for human papillomavirus (HPV) testing, or to respond to a further invitation to undergo a cervical smear. * To ascertain whether such women will attend for further investigation if they have a positive screening test (HPV test or cervical smear). OUTLINE: Patients are randomized to 1 of 2 arms. * Control: Patients receive an invitation for a routine cervical smear and a cervical screening survey. Information regarding attendance for smear or colposcopy is collected at the Primary Care Trust. * Study (self-sampling kit): Patients receive an explanatory letter, an information sheet about the study, a consent form, information about human papillomavirus (HPV) and HPV testing, a self-sampling test kit, and an invitation to take their own HPV sample and return it to the research group for processing. Patients also receive a cervical screening survey. Patients who attend for further investigation following a positive HPV result go to St. Mary's Hospital Colposcopy Unit, Paddington. During this visit cervical smear tests are performed and women are offered immediate colposcopy so that they would not need to return for colposcopic examination if their smear test is abnormal. This study is peer reviewed and funded or endorsed by cancer research UK.

Interventions

OTHEReducational intervention
OTHERsurvey administration
PROCEDUREcolposcopy

Sponsors

Barts and the London School of Medicine and Dentistry
Lead SponsorOTHER

Eligibility

Sex/Gender
FEMALE
Age
25 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

DISEASE CHARACTERISTICS: * Women in Westminster Primary Care Trust (PCT) area eligible for routine cervical screening who have not responded to two invitations to attend for smears * No women who have written to the PCT to document their refusal to take part in the National Health Service Cervical Screening Program (NHSCSP) * No women who are not due for routine screening as part of the NHSCSP PATIENT CHARACTERISTICS: * Not pregnant * Have been sexually active PRIOR CONCURRENT THERAPY: * No prior total abdominal hysterectomy

Design outcomes

Primary

MeasureTime frame
Comparison of the percentages of women responding to the invitation to return a self-sampling kit vs responding to an invitation for a cervical smear

Secondary

MeasureTime frame
Response to the invitation for further investigation following a positive test result (colposcopy for women with a smear showing mild dyskaryosis or above, smear +/- colposcopy for those with a positive HPV test)
Response to the request to return a survey regarding demographic information and reasons for previous non-attendance for screening

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026