N/A
N=985
Rural Interventions for Screening Effectiveness
Breast, Cervical or Colorectal Cancer Screening Needed
Bottom Line
View on ClinicalTrials.gov: NCT02795104 ↗Enrolled (actual)
985
Serious AEs
0.0%
Results posted
Oct 2023
Primary outcome: Primary: Percentage of Participants Who Received All Needed Screening and Any Needed Screening Across the Three Randomized Arms — 57; 118; 19; 110 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Educational Intervention via brochure (Behavioral); Educational Intervention via DVD (Behavioral); Educational Intervention-DVD & Telephone Based Navigation (Behavioral)
- Age
- Adult, Older Adult · 50+ yrs
- Sex
- Female
- Sponsor
- Ohio State University Comprehensive Cancer Center
- Primary completion
- Jul 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Participants Who Received All Needed Screening and Any Needed Screening Across the Three Randomized Arms |
57; 118; 19; 110; 189; 48 | — |
| SECONDARY Cost Effectiveness of Each Intervention |
14,462.64; 10,638.20; 0 | — |
| SECONDARY Cost of the Interventions |
326,012.29; 670,841.46; 0 | — |
Summary
This randomized clinical trial studies how well a tailored interactive digital versatile disc (DVD) with or without patient navigation works in improving screening rates in rural women for breast cancer, cervical cancer or colorectal cancer. A tailored interactive DVD and patient navigation may help rural women to learn more about cancer screening and to better understand the results.
Eligibility Criteria
Inclusion Criteria
- Be non-adherent to one or more recommended screenings for BC, CC, or CRC by Medical Record Review (MRR)
- Reside in one of 32 rural counties in Indiana (IN) or Ohio (OH)
- Provide informed consent
- Able to speak/read English
- Have access to a DVD player or computer that can play DVDs
Exclusion Criteria
- Have a personal or family history of any hereditary/genetic cancer syndrome such as BRCA1 and BRCA2 polymorphisms, hereditary nonpolyposis colon cancer, or familial adenomatous polyposis
- Have a personal history of inflammatory bowel disease (Crohn's disease or colitis), colon polyps, or a history of cancer except non-melanoma skin cancer
- Have a first degree relative with a history of breast or colorectal cancer
- Plan to move outside of the country within the next year
- Reside in a nursing home or other institution
- Are pregnant or intend to become pregnant during the study period
Data sourced from ClinicalTrials.gov (NCT02795104). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.