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Colorectal Cancer Screening clinical trials

View clinical trials related to Colorectal Cancer Screening.

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NCT ID: NCT02419716 Completed - Colorectal Cancer Clinical Trials

A Study of Cologuard™ in an Average Risk Population Assessing a Three Year Test Interval

Start date: April 2015
Phase:
Study type: Observational

This is a prospective longitudinal study to assess the impact of repeat Cologuard testing at 3 years in average risk patients.

NCT ID: NCT02273206 Completed - Depression Clinical Trials

Collaborative Care to Reduce Depression and Increase Cancer Screening Among Low-Income Urban Women

PCM3
Start date: January 2014
Phase: N/A
Study type: Interventional

Bronx County, New York is the poorest urban county in the U.S.A., and residents are almost entirely Latino or African American. Cancer is the leading cause of premature death in the Bronx, with morality rates significantly higher than for New York City as a whole. Low-income/minority populations are more likely to be diagnosed with preventable and late-stage cancers than the general population, in part, due to lower screening rates. While research has addressed screening barriers in low-income/minority groups, depression, a common,potentially critical barrier, has received scant attention. Research suggests that depressed women are less likely to engage in cancer screening, especially mammography and Pap testing. The link between mental health and cancer screening is particularly important to address in the Bronx, which has the highest rates of self-reported serious psychological distress (a measure closely related to depression) in New York City. Depression affects almost 1 in 4 minority women, and while minorities often seek help for depression in primary care, primary care depression management often does not meet evidence-based standards. Drawing on the expertise and close collaboration of Bronx medical and social service providers and patient stakeholders, this study will determine whether a collaborative care intervention that addresses both depression and cancer screening needs simultaneously among women ages 50-64 is more effective at improving cancer screening and patient-reported outcomes for women with depression than an existing evidence-based cancer screening intervention alone. To achieve this, the investigators will compare the effectiveness of these two interventions using a randomized controlled trial (RCT). In partnership with six Bronx Federally Qualified Health Centers (FQHCs), the investigators will recruit approximately 800 women ages 50-64 who screen positive for depression and are non-adherent with recommended cervical, breast, and/or colorectal cancer screenings. The investigators specific aims are to: 1) compare the impact of the two interventions on patient-reported outcomes, including cancer screening knowledge and attitudes, self-efficacy, depression-related stigma, provider referrals, participation in mental health care, medication adherence, quality of life, satisfaction with care and treatment decisions, and depression; 2) compare the effectiveness of the two interventions in increasing breast, cervical, and colorectal cancer screening; 3) determine whether reducing depression increases the likelihood that low-income women 50-64 will receive cancer screening; 4) determine whether effectiveness of the two interventions in increasing cancer screening varies according to patient characteristics, such as duration of depression, presence of other chronic conditions, and obesity. This study is designed to increase the investigators understanding of how to enhance primary care systems' ability to improve a range of outcomes related to cancer screening and depression among low-income minority women, and how to best support this population in making cancer-screening decisions.

NCT ID: NCT02192034 Completed - Clinical trials for Colorectal Cancer Screening

Optimizing Navigation to Successful Colorectal Cancer Screening

Start date: March 2013
Phase: N/A
Study type: Interventional

Colorectal cancer is the second leading cause of death from cancer in the United States. Two major barriers to successful colorectal cancer screening are appointment keeping and proper bowel preparation. The purpose of this study is to test the efficacy of a patient navigation program to increase colorectal cancer screening at Rush University Medical Center. The investigators hypothesize that colorectal cancer screening will be improved for subjects who utilize a patient navigator.

NCT ID: NCT01885351 Completed - Clinical trials for Colorectal Cancer Screening

An Interactive Preventive Health Record to Increase Colorectal Cancer Screening

MyCRCS
Start date: March 1, 2013
Phase: N/A
Study type: Interventional

This study involves 3 phases that modifies current Interactive Preventative Health Record-Colorectal Cancer Screening (IPHR-CRCS) modules to address each patient's individual colorectal cancer screening (CRCS) knowledge, attitudes, preferences, and test-specific barriers. The study will engage patients, ages 50-75 years who are non-adherent to CRCS, to assess their CRCS test preferences and corresponding test-specific barriers in "real time". Based on patient characteristics (e.g. age, personal and family history, physician CRCS recommendation, CRCS test preferences, top test-specific barriers), tailored messages/videos will appear in the pop-up screens to address/reduce the top patient-reported, test-specific CRCS barriers while incorporating an action plan for CRCS adherence. The investigators hypothesize that modifying the IPHR-CRCS module to address each patient's individual CRCS knowledge, attitudes, preferences, and test-specific barriers will further increase CRCS.

NCT ID: NCT01569620 Completed - Clinical trials for Colorectal Cancer Screening

Improving Colorectal Cancer Screening for Diverse Hispanics in Urban Primary Care

Start date: April 2012
Phase: N/A
Study type: Interventional

The proposed study seeks to investigate the impact of a culturally targeted print educational intervention on rates of colorectal cancer (CRC) screening via colonoscopy among Hispanics. If, as expected, the addition of culturally targeted materials to best clinical practices as compared to a) best clinical practices plus standard materials or b) best clinical practices alone leads to higher rates of CRC screening via colonoscopy then the culturally targeted print educational materials can be easily disseminated among this rapidly growing minority group who have low rates of CRC screening and whose disease is detected at later, less curable stages.

NCT ID: NCT01555450 Completed - Clinical trials for Colorectal Cancer Screening

Study of Patient Navigation to Reduce Social Inequalities

PRADO
Start date: March 2011
Phase: N/A
Study type: Interventional

Variations in participation to the colorectal cancer screening seems to reveal social and geographical inequalities. Our study will investigate whether patient navigation could increase the participation to the colorectal cancer screening and in the same time, reduce the social inequalities.

NCT ID: NCT01534923 Completed - Clinical trials for Colorectal Cancer Screening

Doctor-Patient Communication About Colorectal Cancer Screening

Start date: February 7, 2012
Phase:
Study type: Observational

The purpose of this study is to learn more about doctor-patient communication about colon cancer screening. This study will also look to see if there are differences in those who get colon cancer screening based on the discussion the doctor had with the patient.

NCT ID: NCT01519999 Completed - Clinical trials for Colorectal Cancer Screening

Colorectal Cancer Screening With Improved Shared Decision Making

CRCS-WISDM
Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to increase colorectal cancer screening by implementing a community-wide shared decision-making (SDM) intervention, which embeds shared decision making within clinical practice and also uses an extensive community engagement campaign. The investigators hypothesize that colorectal cancer screening adherence will be higher in the intervention group (participating communities) compared to the usual care control group (non-participating comparison communities).

NCT ID: NCT01250015 Completed - Clinical trials for Colorectal Cancer Screening

Does Numerical And Pictorial Information On Risk And Benefit Affects The Uptake Of Colorectal Cancer Screening?

Start date: September 2007
Phase: N/A
Study type: Observational

To establish whether provision of numerical data, framed as event rates and illustrated by pictograms, and including figures for all-cause mortality, affects subjects' attitudes to colorectal cancer (CRC) screening. Design and Intervention. Randomised questionnaire and telephone study comparing the responses of a control group given the standard National Health Service (NHS) CRC screening information with the responses of an intervention group given the same information but enhanced with additional numerical and pictorial information. Setting

NCT ID: NCT01210235 Completed - Clinical trials for Colorectal Cancer Screening

FLU-FIT Program at Kaiser Permanente Northern California

Start date: October 2009
Phase: N/A
Study type: Interventional

The investigators overall goal is to develop, implement, test, and disseminate an intervention to increase colorectal cancer screening rates at Kaiser Permanente (KP) by providing home fecal immunochemical test kits (FIT) to eligible patients aged 50 and older who participate in annual influenza vaccination campaigns. The investigators hypothesis is that the FLU-FIT Program will be an effective method to increase colorectal cancer screening rates at Kaiser Permanente.