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About
This pilot trial study uses a structural support program for adoption of cancer screening interventions at a rural community-based organization. Rural communities face unique barriers in implementation of evidence-based interventions due to a lack of infrastructure, community capacity, and expertise as academic and research centers are often clustered in urban areas. The support program may help a rural community-based organization select, adapt, and implement cancer prevention and control evidence-based interventions.
Full description
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Community-based organizations participate in the support program, consisting of 2 half-day training workshops over 2 weeks, and 30-minute bi-weekly consultations in order to adapt and implement the cancer screening intervention for community members.
After completion of study, participants are followed up at 3 months.
Enrollment
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Inclusion and exclusion criteria
Inclusion Criteria:
Objective II COMMUNITY-BASED ORGANIZATION: Located in the Yakima Valley of Washington State
Objective II COMMUNITY-BASED ORGANIZATION: Serve community members who are 18 and older
Objective II COMMUNITY-BASED ORGANIZATION: Willing to commit to the 6-month program
Objective II PARTICIPANTS: Receiving services from the recruited community-based organization
Objective III PARTICIPANTS: Not up-to-date for breast, cervical, and colorectal cancer screening according to current U.S. Preventive Services Tasks Force (USPSTF) guidelines. The current USPSTF recommendations for breast, cervical, and colorectal cancer are:
Objective III PARTICIPANTS: If the community-based organization selects breast cancer screening, we will recruit women ages 50-74.
Objective III PARTICIPANTS: If the community-based organization selects cervical cancer screening, we will recruit women ages 21-65.
Objective III PARTICIPANTS: If the community-based organization selects colorectal cancer screening, we will recruit women and men ages 50-75.
Objective III PARTICIPANTS: Average risk for breast, cervical, or colorectal cancer
Primary purpose
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35 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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