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| Sponsor: | University of Pittsburgh |
|---|---|
| Collaborators: |
Association of Schools of Public Health Centers for Disease Control and Prevention |
| Information provided by: | University of Pittsburgh |
| ClinicalTrials.gov Identifier: | NCT00327457 |
Purpose
The investigators aim to use a randomized design to test the effects of 1) tailored physician recommendations, relative to non-specific recommendations, and 2) coordinated physician office management systems on patient adherence to colorectal cancer screening recommendations.
| Condition | Intervention |
|---|---|
|
Preventive Health Services |
Behavioral: Help with physician office and patient management Behavioral: Tailored physician recommendation letter |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Factorial Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Coordinated Endoscopic Colorectal Cancer Screening |
| Enrollment: | 599 |
| Study Start Date: | June 2002 |
| Estimated Study Completion Date: | March 2005 |
The investigators aim to use a randomized design to test the effects of 1) tailored physician recommendations, relative to non-specific recommendations, and 2) coordinated physician office management systems on patient adherence to colorectal cancer screening recommendations.
To accomplish these aims, the investigators propose 1) to use existing physician practice-based computerized patient registration systems to define populations of 50 to 79 year-old pri-mary care patients, 2) to use mailed questionnaires to determine colorectal cancer risk factor status and prior colorectal cancer screening history, 3) to use responses from mailed questionnaires to identify persons not adhering to colorectal cancer screening guidelines, 4) to use computer driven algorithms to help physicians prepare and deliver individually tailored and written colorectal cancer screening recommendations, and 5) to develop, implement, and evaluate a centralized service for delivering high quality screening flexible sigmoidoscopy.
Eligibility| Ages Eligible for Study: | 50 Years to 79 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
-
Exclusion Criteria:
Contacts and Locations| United States, Pennsylvania | |
| University of Pittsburgh Cancer Institute | |
| Pittsburgh, Pennsylvania, United States, 15232 | |
| Principal Investigator: | Joel L. Weissfeld, MD MPH | University of Pittsburgh |
More Information
| ClinicalTrials.gov Identifier: | NCT00327457 History of Changes |
| Other Study ID Numbers: | S1796-21/23 (NCE) |
| Study First Received: | May 16, 2006 |
| Last Updated: | February 18, 2011 |
| Health Authority: | United States: Federal Government |
|
colorectal cancer screening sigmoidoscopy colonoscopy |
|
Colorectal Neoplasms Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms |
Digestive System Diseases Gastrointestinal Diseases Colonic Diseases Intestinal Diseases Rectal Diseases |