Self-Sampling in Women Who Do Not Undergo Routine Cervical Screening
Primary Purpose
Health Status Unknown, Precancerous Condition
Status
Completed
Phase
Locations
United Kingdom
Study Type
Observational
Intervention
compliance monitoring
cervical Papanicolaou test
educational intervention
screening questionnaire administration
survey administration
colposcopy
Sponsored by
About this trial
This is an observational trial for Health Status Unknown focused on measuring human papilloma virus infection, health status unknown
Eligibility 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
Sites / Locations
- Barts and the London School of Medicine
Outcomes
Primary Outcome Measures
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 Outcome Measures
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
Full Information
NCT ID
NCT00977392
First Posted
September 12, 2009
Last Updated
August 6, 2013
Sponsor
Barts and the London School of Medicine and Dentistry
1. Study Identification
Unique Protocol Identification Number
NCT00977392
Brief Title
Self-Sampling in Women Who Do Not Undergo Routine Cervical Screening
Official Title
The Potential Role of Self-sampling in Women Who do Not Attend for Cervical Screening - a Randomised Controlled Trial
Study Type
Observational
2. Study Status
Record Verification Date
September 2009
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
March 2011 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Barts and the London School of Medicine and Dentistry
4. Oversight
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Health Status Unknown, Precancerous Condition
Keywords
human papilloma virus infection, health status unknown
7. Study Design
Enrollment
3000 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
compliance monitoring
Intervention Type
Other
Intervention Name(s)
cervical Papanicolaou test
Intervention Type
Other
Intervention Name(s)
educational intervention
Intervention Type
Other
Intervention Name(s)
screening questionnaire administration
Intervention Type
Other
Intervention Name(s)
survey administration
Intervention Type
Procedure
Intervention Name(s)
colposcopy
Primary Outcome Measure Information:
Title
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 Outcome Measure Information:
Title
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)
Title
Response to the request to return a survey regarding demographic information and reasons for previous non-attendance for screening
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne Szarewski, MD
Organizational Affiliation
Queen Mary University of London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barts and the London School of Medicine
City
London
State/Province
England
ZIP/Postal Code
SW15 5PN
Country
United Kingdom
12. IPD Sharing Statement
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/21343937
Description
HPV self-sampling as an alternative strategy in non-attenders for cervical screening - a randomised controlled trial. Br J Cancer. 2011 Mar 15;104(6):915-20. doi: 10.1038/bjc.2011.48. Epub 2011 Feb 22.
Learn more about this trial
Self-Sampling in Women Who Do Not Undergo Routine Cervical Screening
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