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Activating Collaborative CIS Support Via Targeted Provider Mailing

Not Applicable
Completed
Conditions
Precancerous Condition
Interventions
Other: Usual care mailing intervention
Other: CIS support mailing intervention
Registration Number
NCT00873288
Lead Sponsor
Northwestern University
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
254
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Usual Care mailing interventionUsual care mailing interventionroutine colposcopy reminder letter mailed
CIS support mailing interventionCIS support mailing interventionMailed reminder plus provider recommendation to call CIS and sample questions to ask
Primary Outcome Measures
NameTimeMethod
Patient Satisfaction in the 2 Interventionswithin 6 months of PAP

Patient satisfaction with provider-patient communication was assessed via administration of the Consumer Assessment of Health Plans Study (CAHPS) satisfaction questionnaire which rates satisfaction on a 1 to 3 scale. Scores are added together, with minimum score being 4 and the maximum score being 12, with a higher score indicating greater satisfaction.

CIS Experience of Patients in Arm II and the Effect of the Intervention on Their Follow-up Colposcopywithin 6 months of PAP
Secondary Outcome Measures
NameTimeMethod
Number of CIS Callers Who Provided the Specific Codes Listed in the Intervention LetterWITHIN 6 MONTHS OF PAP
Latency Between the Pap Test and the Colposcopy Appointmentwithin 6 months of PAP
Attendance at a Follow-up Colposcopy Appointment Within 6 Months of Their Pap Testwithin 6 months of PAP

Trial Locations

Locations (2)

Robert H. Lurie Comprehensive Cancer Center at Northwestern University

🇺🇸

Chicago, Illinois, United States

Erie Family Health Center

🇺🇸

Chicago, Illinois, United States

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