Facilitating Follow-Up Adherence for Abnormal Pap Smears (TC3)
Uterine Cervical Neoplasms
About this trial
This is an interventional prevention trial for Uterine Cervical Neoplasms focused on measuring cervical cancer, follow-up, Pap test, Medical management, Colposcopy
Eligibility Criteria
Inclusion Criteria:
- women 18 years old or older
- have recently received an abnormal Pap smear indicative of oncogenic HPV
- have been referred for initial colposcopic evaluation at the Women's Care Center at Temple University Hospital
- able to communicate with ease in English
Exclusion Criteria:
- unable to communicate readily in English
- do not have access to a telephone
- have a history of any malignancy
- display current evidence of positive invasive carcinoma of the cervix
- display presence of another life-threatening medical condition
- show evidence of dementia
- prior participation in research study
- HIV
Sites / Locations
- Fox Chase Cancer Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Cognitive-affective barriers counseling delivered by phone
cognitive-affective barriers counseling via brochure
standard care
Standard care plus cognitive-affective barriers counseling delivered by phone , i.e., culturally-relevant/sensitive barrier-specific messages drawn from a pre-developed library designed to counsel individuals regarding their specific barriers to adherence
Standard care plus cognitive-affective barriers counseling delivered via mail-home print material
Cognitive-affective barriers (CAB) assessment delivered via phone; receipt of a notification letter from physician regarding abnormal Pap test result, need to undergo colposcopy, appointment date and clinic contact numbers; telephone confirmation and post-card appointment reminder