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Unidas Por Vida y Salud: Increasing Breast and Cervical Cancer Screening in El Paso

Unidas Por Vida y Salud: Increasing Breast and Cervical Cancer Screening in El Paso

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04397744
Enrollment
660
Registered
2020-05-21
Start date
2015-01-16
Completion date
2017-10-17
Last updated
2020-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Cervical Cancer

Keywords

Mammogram, Pap test

Brief 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.

Interventions

BEHAVIORALUnidas 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.

Sponsors

Cancer Prevention Research Institute of Texas
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* overdue for a repeat mammogram * overdue for repeat cervical screening

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frame
Number of participants who uptake clinical breast exam (CBE)6 months
Number of participants who uptake mammography6 months
Number of participants who uptake pap test6 months
Number of participants who repeat mammography6 months
Number of participants who repeat pap test6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026