We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01773980
First Posted: January 23, 2013
Last Update Posted: May 22, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
National Institutes of Health (NIH)
Information provided by (Responsible Party):
OHSU Knight Cancer Institute
  Purpose
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.

Condition Intervention
Breast Cancer Cervical Cancer Colorectal Cancer Other: Clinic Intervention Other: Patient Intervention

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Prospective
Official Title: Activating Rural Clinics and Women With Disabilities to Improve Cancer Screening

Resource links provided by NLM:


Further study details as provided by OHSU Knight Cancer Institute:

Primary Outcome Measures:
  • Number of participants with improved cancer screening [ Time Frame: Duration of the study; Up to 1 year ]
    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).


Enrollment: 1570
Study Start Date: August 2013
Study Completion Date: April 2015
Primary Completion Date: April 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
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.

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.
Other: Patient Intervention
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.
Other: Patient Intervention
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.
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.
Neither Clinic nor Patient Intervention
Consists of no intervention

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   50 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Primary care clinics
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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01773980


Locations
United States, Oregon
OHSU Knight Cancer Institute
Portland, Oregon, United States, 97239
Sponsors and Collaborators
OHSU Knight Cancer Institute
National Institutes of Health (NIH)
Investigators
Principal Investigator: David Buckley, MD Oregon Health and Science University
  More Information

Responsible Party: OHSU Knight Cancer Institute
ClinicalTrials.gov Identifier: NCT01773980     History of Changes
Other Study ID Numbers: IRB00009030
First Submitted: January 18, 2013
First Posted: January 23, 2013
Last Update Posted: May 22, 2015
Last Verified: May 2015

Additional relevant MeSH terms:
Colorectal Neoplasms
Uterine Cervical Neoplasms
Intestinal Neoplasms
Gastrointestinal Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Neoplasms
Uterine Neoplasms
Genital Neoplasms, Female
Urogenital Neoplasms
Genital Diseases, Female
Digestive System Diseases
Gastrointestinal Diseases
Colonic Diseases
Intestinal Diseases
Rectal Diseases
Uterine Cervical Diseases
Uterine Diseases