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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00476970
Other study ID # 2006P 002254
Secondary ID
Status Completed
Phase N/A
First received May 21, 2007
Last updated September 20, 2016
Start date September 2007
Est. completion date September 2008

Study information

Verified date September 2016
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The goal of this study is to implement and in a controlled randomised trial test a program to identify and overcome barriers to CRC screening and thus improve CRC screening rates at MGH Chelsea HC.

Our hypothesis is that a bilingual navigator program, enhanced by using trained interpreting staff will improve CRC screening rates at MGH Chelsea HC overall, and decrease disparities between patients with limited English proficiency and English speakers


Description:

We developed a training program for five health center interpreters fluent in eight different languages. Patients randomly assigned to the study intervention receive an introductory letter in their native language. During the initial contact the navigator educates patients about CRC screening and explores patients' barriers to CRC screening. Based on results from a qualitative study conducted at in 2006, we developed interventions to overcome individual barriers to CRC screening tailored to each individual patient. Specific interventions include elucidation of culturally-specific health beliefs; teaching about cancer risk, colonoscopy, and colon prep administration; and help with appointment-making and transport.


Recruitment information / eligibility

Status Completed
Enrollment 1223
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 52 Years to 79 Years
Eligibility Inclusion Criteria:

- Between 52-79 years of age

- Have not had a colonoscopy within the last 10 years

- Have not had a sigmoidoscopy/barium enema within the past 5 years

- Have not had a home fecal occult blood testing within the past year.

Exclusion Criteria:

- Acutely ill

- Dementia

- Metastatic cancer

- Schizophrenia

- Any end stage disease

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


Intervention

Behavioral:
Patient Navigation
Patient navigators will perform an initial interview with participants to identify and explore barriers, work with patients to overcome barriers, educate patients about CRC screening, motivate and coach patients, and schedule and accompany patients to colonoscopy testing

Locations

Country Name City State
United States MGH Chelsea Health Center Chelsea Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Eligible Patients In Study and Control Groups Who Undergo CRC Screening 18 Months No
Secondary Type of CRC Screening Test Performed in Study vs Control Groups 18 Months No
Secondary Number of Polyps and Cancers per 100 Patients in the Study vs Control Group 18 Months No
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