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

NCT ID: NCT01773980

Last Updated: 2015-05-22

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 1570 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-08-31
• Study Completion Date: 2015-04-30

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.

Conditions

Breast Cancer; Cervical Cancer; Colorectal Cancer

Study Design

• Observational Model Type: ECOLOGIC_OR_COMMUNITY
• Study Time Perspective: PROSPECTIVE

Study Groups

Patient and Clinic Intervention

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

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.

Clinic Intervention

Intervention Type: OTHER

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

Intervention Type: OTHER

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

Patient Intervention Only

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

Patient Intervention

Intervention Type: OTHER

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

Clinic Intervention Only

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.

Clinic Intervention

Intervention Type: OTHER

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.

Neither Clinic nor Patient Intervention

Consists of no intervention

No interventions assigned to this group

Interventions

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.

Intervention Type: OTHER

Patient Intervention

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

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

OHSU Knight Cancer Institute

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David Buckley, MD

Role: PRINCIPAL_INVESTIGATOR

Oregon Health and Science University

Locations

OHSU Knight Cancer Institute

Portland, Oregon, United States

Countries

United States

Other Identifiers

IRB00009030

Identifier Type: -

Identifier Source: org_study_id