Personalized Letter With Cancer Information Service Support or a Standard Reminder Letter in Women Scheduled for Colposcopy After an Abnormal Pap Test

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by National Cancer Institute (NCI).
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Information provided by:
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT00873288
First received: March 31, 2009
Last updated: January 27, 2010
Last verified: March 2009

March 31, 2009
January 27, 2010
October 2006
September 2009   (final data collection date for primary outcome measure)
  • Patient satisfaction in the 2 interventions [ Designated as safety issue: No ]
  • CIS experience of patients in arm II and the effect of the intervention on their follow-up colposcopy [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00873288 on ClinicalTrials.gov Archive Site
  • Attendance at a follow-up colposcopy appointment within 6 months of their Pap test [ Designated as safety issue: No ]
  • Latency between the Pap test and the colposcopy appointment [ Designated as safety issue: No ]
  • Number of CIS callers who provided the specific codes listed in the intervention letter [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Personalized Letter With Cancer Information Service Support or a Standard Reminder Letter in Women Scheduled for Colposcopy After an Abnormal Pap Test
Activating Collaborative CIS Support Via Targeted Provider Mailing

RATIONALE: Receiving a reminder letter from their doctor with questions to ask the Cancer Information Service may be more effective than a standard reminder letter in helping patients who have had an abnormal Pap test keep their follow-up colposcopy appointment.

PURPOSE: This randomized clinical trial is studying a personalized letter with Cancer Information Service support to see how well it works compared with a standard reminder letter in women scheduled for colposcopy after an abnormal Pap test.

OBJECTIVES:

  • Compare the effect of a usual care mailing intervention vs a Cancer Information Service (CIS) support mailing intervention on the likelihood that women with an abnormal Pap test will keep their medical follow-up appointments and be satisfied with how they talk to their provider.

OUTLINE: This is a multicenter study. Patients are randomized to 1 of 2 intervention arms.

  • Arm I (Usual-care mailing intervention): Patients receive a generic letter reminding them of their follow-up colposcopy appointment.
  • Arm II (Cancer Information Service [CIS] support mailing intervention): Patients receive a targeted letter reminding them of their follow-up colposcopy appointment, asking them or someone they designate to call the CIS, and suggesting some questions to ask the CIS about colposcopies and Pap tests.

At their follow-up appointments, all patients undergo an exit interview to compare patient satisfaction between the 2 interventions. Patients in arm II also answer questions about their CIS experience, and if the intervention made their follow-up visit less difficult.

Interventional
Not Provided
Allocation: Randomized
Primary Purpose: Health Services Research
Precancerous Condition
  • Other: informational intervention
  • Other: questionnaire administration
Not Provided
Cofta-Woerpel L, Randhawa V, McFadden HG, Fought A, Bullard E, Spring B. ACCISS study rationale and design: activating collaborative cancer information service support for cervical cancer screening. BMC Public Health. 2009 Dec 2;9:444.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
500
Not Provided
September 2009   (final data collection date for primary outcome measure)

DISEASE CHARACTERISTICS:

  • Received an abnormal Pap test result
  • Scheduled for a colposcopy within 6 months of their Pap test at either the Erie Family Health Center or the Prentice Ambulatory Clinic

PATIENT CHARACTERISTICS:

  • Able to communicate in either English or Spanish
  • Clinic staff will review patient charts to determine eligibility

PRIOR CONCURRENT THERAPY:

  • Not specified
Female
18 Years and older
No
Not Provided
United States
 
NCT00873288
CDR0000626557, NU-1719-007
Not Provided
Not Provided
Robert H. Lurie Cancer Center
National Cancer Institute (NCI)
Principal Investigator: Bonnie Spring, PhD Robert H. Lurie Cancer Center
National Cancer Institute (NCI)
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP