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

Breast Cancer Clinical Trial

Official title:

Activating Rural Clinics and Women With Disabilities to Improve Cancer Screening

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01773980
• Other study ID #: IRB00009030
• Status: Completed
• Phase: N/A
• First received: January 18, 2013
• Last updated: May 20, 2015
• Start date: August 2013
• Est. completion date: April 2015

Study information

• Verified date: May 2015
• Source: OHSU Knight Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1570
• Est. completion date: April 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 50 Years to 75 Years

Eligibility

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

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective

Related Conditions & MeSH terms

• Breast Cancer
• Cervical Cancer
• Colorectal Cancer
• Uterine Cervical Neoplasms

Intervention

Other:
• Clinic 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.
• Patient Intervention
The patient intervention consists of a single 90-minute interactive in-person session.

Locations

Country	Name	City	State
United States	OHSU Knight Cancer Institute	Portland	Oregon

Sponsors (2)

Lead Sponsor	Collaborator
OHSU Knight Cancer Institute	National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with improved cancer screening	A 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).	Duration of the study; Up to 1 year	No