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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04397744
Other study ID # HSC-SPH-12-0677
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2015
Est. completion date October 17, 2017

Study information

Verified date May 2020
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop, implement and evaluate a comprehensive breast and cervical cancer screening program designed to increase uptake of breast and cervical cancer screening among rarely and never-screened low-income women in El Paso County and to increase repeat screening among those currently overdue.


Recruitment information / eligibility

Status Completed
Enrollment 660
Est. completion date October 17, 2017
Est. primary completion date October 17, 2017
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 64 Years
Eligibility Inclusion Criteria:

- overdue for a repeat mammogram

- overdue for repeat cervical screening

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Unidas por Vida y Salud prevention program
The Unidas por Vida y Salud (United for Life and Health) prevention program is led by the El Paso Cancer and Chronic Disease Consortium (CCDC), the only Breast and Cervical Cancer Services (BCCS) provider in El Paso. This prevention program will use a well-integrated network of community organizations and health service providers to connect medically underserved women to services. To reach the most underserved women and increase preventive cancer screening and timely follow-up, diagnosis, and treatment, the multi-method approach uses evidence-based strategies, including face-to-face educational sessions led by promotoras (community health workers), client reminders, and provision of community-based navigation services to affordable and free screening services. The program also includes clinic-based navigation for those requiring diagnostics or treatment delivered by trained nurses and case workers.

Locations

Country Name City State
United States The University of Texas Health Science Center at Houston Houston Texas

Sponsors (2)

Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston Cancer Prevention Research Institute of Texas

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants who uptake clinical breast exam (CBE) 6 months
Primary Number of participants who uptake mammography 6 months
Primary Number of participants who uptake pap test 6 months
Primary Number of participants who repeat mammography 6 months
Primary Number of participants who repeat pap test 6 months
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