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

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Georgetown University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Colorectal Cancer

Treatments

Behavioral: Mailed printed materials and in-office training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01289288
2007-297
R01CA121023 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full description

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.

Enrollment

480 patients

Sex

All

Ages

50 to 74 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For Physicians

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

For Patients

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

Exclusion criteria

For Patients:

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

480 participants in 2 patient groups

Mailed printed materials and in-office training
Experimental group
Treatment:
Behavioral: Mailed printed materials and in-office training
Control
No Intervention group
Description:
Usual care

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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