Skip to content

CROSSROAD II: Activating Rural Clinics and Women With Disabilities to Improve Cancer Screening

Activating Rural Clinics and Women With Disabilities to Improve Cancer Screening

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01773980
Enrollment
1570
Registered
2013-01-23
Start date
2013-08-31
Completion date
2015-04-30
Last updated
2015-05-22

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

Conditions

Breast Cancer, Cervical Cancer, Colorectal Cancer

Brief summary

The goal of this project is to develop and pilot test an innovative approach for overcoming barriers to cancer screening among women with physical disabilities (WWD) in rural Oregon. Many studies have shown that people with disabilities receive fewer indicated cancer screening services and are more likely to have poor cancer-related outcomes, such as late stage at diagnosis, compared to those without disabilities.

Interventions

OTHERClinic Intervention

The Clinic intervention consists of an educational video, an interactive meeting with clinicians and clinic staff, and a facilitated follow-up meeting with clinic staff.

The patient intervention consists of a single 90-minute interactive in-person session.

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
OHSU Knight Cancer Institute
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Female * Aged 50-75 at time of screening * No personal history of breast, cervical or colorectal cancer * Not being up-to-date with at least one screening test for breast, cervical, and/or colorectal cancer * Meets the study definition of disability per screening survey OR * Be a woman who does not meet the definition of disability per screening survey, but has been matched to a participant who does (observation group).

Exclusion criteria

* Non female * Personal history of breast, cervical, or colorectal cancer * Coming into clinic for an urgent care issue

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with improved cancer screeningDuration of the study; Up to 1 yearA 2 x 2 factorial study design will be used to explore individual and combined effects of a clinic-based intervention AND a patient-based intervention on improving breast, cervical and colorectal cancer screening among rural women with physical disabilities (WWD).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026