Tailored Interactive Intervention to Increase CRCS (PCCaSO)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01084746|
Recruitment Status : Completed
First Posted : March 10, 2010
Last Update Posted : May 11, 2018
|Condition or disease||Intervention/treatment||Phase|
|Colorectal Cancer Screening||Behavioral: PC-based tailored intervention Behavioral: Printed educational materials||Not Applicable|
Specific Aim 1: Identify behavioral, social, and environmental factors associated with CRCS in male and female patients ages 50 to 64 years old in a primary care practice in Houston, Texas.
1.1. Update literature reviews of CRCS adherence. 1.2. Conduct secondary analysis of relevant data from other projects. 1.3. Conduct focus groups with primary care patients to determine their knowledge, attitudes, and beliefs about CRCS and to gather data to use for development of the educational intervention.
Specific Aim 2: Develop a personal computer (PC)-based tailored interactive intervention based on the transtheoretical (stages of change) model to increase CRCS in accordance with American Cancer Society (ACS) CRCS guidelines.
Specific Aim 3: Evaluate the effectiveness of the PC-based tailored interactive intervention for increasing CRCS through a randomized controlled trial.
Specific Aim 4: Analyze the relationship between a number of predictor variables and CRCS completion in order to develop a more complete conceptual framework for understanding screening adherence.
Specific Aim 5: Conduct a cost-effectiveness analysis of the PC-based tailored interactive intervention for increasing CRCS in a primary care setting.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||1224 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Care Provider)|
|Official Title:||Tailored Interactive Intervention to Increase CRCS|
|Study Start Date :||January 2005|
|Actual Primary Completion Date :||June 2008|
|Actual Study Completion Date :||June 2008|
|Active Comparator: PC-based tailored intervention||
Behavioral: PC-based tailored intervention
Patients will receive a tailored interactive PC-based intervention at a freestanding kiosk.
|Active Comparator: Printed educational materials||
Behavioral: Printed educational materials
Patients will receive generic printed educational materials about CRCS in the PEC when they arrive at the Main Campus for their appointment.
No Intervention: No patient intervention
Patients will not receive a patient-directed intervention.
- Increase patient completion of colorectal cancer screening (CRCS) among patients ages 50 to 64 years old. [ Time Frame: 6months, 12months, 24 months ]6, 12, and 24 months post intervention, medical charts were reviewed to validate self-reported CRCS behavior.
- Secondary goals are to increase understanding of factors that predict completion of CRCS and to assess the cost-effectiveness of the intervention. [ Time Frame: 6 months, 12 months, 24 months ]Survey data were collected at 6,12,and 24 months.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01084746
|United States, Texas|
|University of Texas Health Science Center at Houston School of Public Health|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Sally W Vernon, PhD||The University of Texas Health Science Center, Houston|