Reducing Urban Cervical Cancer Disparities

Recruiting N/A Interventional Study
Cervical Cancer Papilloma Viral Infection
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 90
Sex
Female
Study type
Interventional
Purpose
Screening
Participants needed
546 (estimated)
Sponsor
Fox Chase Cancer Center · Other
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About This Trial

This study uses a hybrid Type 1 effectiveness-implementation trial to operationalize and assess the efficacy of the Health Enhancement Resource System (HERS) intervention. HERS aims to increase patient follow-up after abnormal test results through text message-based barriers counseling for women and supplemental telephone-based Health Coaching for women who miss their appointment.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 18 to 90 years of age (screening is still recommended for some women over 65-depending on screening and medical history and proceeds until age 90 in the study's clinic recruitment sites), * referral for colposcopic evaluation at the clinic sites, * able to communicate with eas…
Contacts

Suzanne M Miller, PhD

215-728-4069

suzanne.miller@fccc.edu

CONTACT

Erin K Tagai, PhD, MPH

215-728-5621

erin.tagai@fccc.edu

CONTACT