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Completed

NCT Number: NCT01289288

A Physician-Based Trial to Increase Colorectal Cancer Screening in Chinese

The objective of this study is to test whether a culturally-tailored in-office based intervention have impact on increasing Chinese physician's recommendation of colorectal cancer (CRC) screening to their nonadherent Chinese patients.

Special aims are to:

1. Evaluate the efficacy of a culturally-tailored physician intervention on increasing non-adherent Chinese American's patients' CRC screening rate. 2. Identify factors that mediate or moderate the intervention effects. For example, patients who hold an eastern cultural view or are less acculturated will be more likely to benefit from the intervention than patients who hold a western view or who are more acculturated.

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Key information

Age range

50 year–74 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Georgetown University, Washington D.C., District of Columbia, United States

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About this study

This study is a randomized controlled trial aiming to test the effect of the culturally-tailored in-office based intervention on physicians. A total of 24 Chinese physicians in the Washington DC and Philadelphia areas and a total of 24 eligible Chinese patients from each physician will be recruited for this study. Physicians and their patients are randomized into two groups: A and B. Physician in the intervention group (A) will receive mailed printed materials including a CRC physician guide, patient brochure, flip chart and a poster and two sessions of in-office training aimed to reinforce learning of the topic covered by the mailed materials and provide physicians with hands-on experience in using communication skills with standardized patients. Physicians in the control group (B) will receive nothing until the end of the study. Patients will be followed 12-month later after their completion of the baseline survey and their self-reported CRC screening status will be verified by chart audit.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

For Physicians

  • are Chinese American,
  • practice primary care,
  • have a least 75 Chinese patients aged 50 and older in their practice,
  • can communicate with patients in Chinese (Mandarin, Cantonese, etc.)

For Patients

  • visiting the participating physician at least once in the past 2 years,
  • are Chinese Americans,
  • are 50 years and older,
  • never had any CRC screening or are overdue for screening.

Exclusion criteria

For Patients:

  • have a colorectal polyp, CRC cancer, or a family history of CRC (first degree relative), and
  • had updated CRC screening (FOBT within one year, colonoscopy within 10 years, sigmoidoscopy within 5 years and double-contrast barium enema within 5 years).

Treatment and study plan

Mailed printed materials and in-office training

Behavioral
  • Mailed printed materials including CRC physician guide, patient brochure, flip chart and a poster
  • Two sessions of in-office training with two standardized patients

Primary outcomes

  1. Receipt of CRC screening

    Time frame: 12 months

    Nonadherent Chinese American patient's CRC screening rates.

Sponsors and collaborators

Lead sponsor

Georgetown University

Other

Collaborators

  • National Cancer Institute (NCI)
  • Temple University

Registry information

Acronym: CRC

Important dates

Study start
2007
Primary completion
2012
Study completion
2012
First posted
Feb 3, 2011
Registry last updated
May 21, 2013

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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