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Completed

NCT Number: NCT01351220

Community Dissemination of an Evidence-based Colorectal Cancer (CRC) Screening Intervention

Filipino Americans have lower rates of colorectal cancer (CRC) screening, later stage of diagnosis and poorer survival relative to other racial/ethnic groups. To address this disparity, the investigators developed a multi-component intervention to increase CRC screening and have determined its efficacy in a randomized trial (Maxwell,et. al., 2010). This study aims to determine how an intervention to increase CRC screening can best be integrated within the cultural norms and existing structures of churches and community based organizations (CBOs) with predominantly Filipino American membership to ensure broad dissemination to those in need of screening.

The investigators will provide our partner CBOs with resources and technical assistance, including training of community volunteers as health advisors, to enable them to promote CRC screening to their constituents. Using a scientifically rigorous research design, the investigators will compare two dissemination strategies: Basic dissemination which consists of a single kick-off event during which community health advisors will receive print materials and FOBT kits for distribution and training on how to conduct educational small-group sessions; and Organizational dissemination aimed at integrating CRC screening dissemination into organizational practices and processes that can be sustained after the end of the study. The study will be implemented in 20 CBOs and will train 100 community health advisors (CHAs). The impact of the two dissemination strategies will be comprehensively assessed by collecting data at the CBO level, from the CHAs and from 1000 Filipino American participants. The investigators will compare the proportion of Filipino American participants who obtain CRC screening by dissemination strategy, but the investigators will also assess how many are reached, if the intervention is implemented as planned, how CBOs support the screening efforts at their regular activities, and if CBOs and CHAs maintain their efforts over the 4 years of the study.

The investigators hypothesize that CBOs can implement evidence-based strategies to promote CRC screening and CHAs in the organizational dissemination arm will reach more participants and more screened participants than CHAs in the basic dissemination arm; and organizations in the organizational dissemination arm will adopt more CRC screening activities and maintain these better than organizations in the basic dissemination arm.

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Key information

Age range

50 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UCLA Division of Cancer and Prevention Research

Los Angeles, California, 90095-6900, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Filipino American
  • 50 to 75 years of age
  • Must not have been diagnosed with CRC
  • Must not be adherent to USPSTF CRC screening guidelines

Exclusion criteria

  • Not Filipino American
  • Younger than 50 or older than 75 years of age
  • Have been diagnosed with CRC
  • Adherent to USPSTF CRC screening guidelines

Treatment and study plan

Educational program and FOBT kits

Behavioral

Subjects will participate in a CRC small group educational program and receive FOBT kits from community health advisors who have received a one-time training session.

Educational program and FOBT kits, and technical assistance

Behavioral

In addition to subjects' receipt of a CRC small group educational program and FOBT kits, leadership training and technical support will be provided to the community health advisors and selected leaders and members of the organization.

Primary outcomes

  1. Change from Baseline in receipt of CRC screening at 6 months and 24 months

    Time frame: baseline, 6-month and 24-month post intervention

    Subjects will receive any one of the 3 recommended CRC screening tests namely, Fecal Occult Blood Test, Flexible sigmoidoscopy or Colonoscopy

Secondary outcomes

  1. Change from Baseline in intention to obtain screening at 6 months and 24 months

    Time frame: baseline, 6-months and 24-months after exposure to the intervention

  2. Change from Baseline in CRC screening knowledge at 6 months and 24 months

    Time frame: baseline, 6 months and 24 months after exposure to the educational program

  3. Change from Baseline in frequency of patient provider communication at 6 months and 24 months

    Time frame: baseline, 6 and 24 months after exposure to the intervention

Sponsors and collaborators

Lead sponsor

Jonsson Comprehensive Cancer Center

Other

Collaborators

  • American Cancer Society, Inc.

Registry information

Official study title

Community Dissemination of an Evidence-based CRC Screening Intervention

Important dates

Study start
2010
Primary completion
2014
Study completion
2015
First posted
May 10, 2011
Registry last updated
Aug 1, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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