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Colorectal Cancer Screening clinical trials

View clinical trials related to Colorectal Cancer Screening.

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NCT ID: NCT04131946 Completed - Clinical trials for Colorectal Cancer Screening

Cancer Screening; Access; Awareness; Navigation

Start date: November 12, 2019
Phase: N/A
Study type: Interventional

To assess the feasibility and efficacy of community-based Colorectal Cancer (CRC) screening intervention in increasing CRC screening rates To evaluate individual-level knowledge related to CRC screening and risk factors To characterize individual -level facilitators and barriers to engaging in CRC screening and related diagnostic tests and treatment when applicable.

NCT ID: NCT03974542 Not yet recruiting - Clinical trials for Colorectal Cancer Screening

Telephone Outreach by Navigators to Improve Repeat Fecal Occult Blood Testing

Start date: October 2019
Phase: N/A
Study type: Interventional

To conduct a randomised control trial to test the effectiveness of telephone outreach programme to improve the uptake rate of repeat fecal occult blood test in colorectal cancer screening programme.

NCT ID: NCT03959696 Active, not recruiting - Clinical trials for Colorectal Cancer Screening

Promoting Informed Decisions About Cancer Screening in Older Adults

PRIMED
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

This project aims to examine the impact of different interventions designed to help individualize colorectal cancer (CRC) screening decisions in adults aged 76-85. Clinicians will be assigned by chance to one of two arms. In the Intervention arm, clinician participants will complete a training course and will also be notified of patients in the target age group who are due for a discussion about CRC screening. In the Comparator arm, clinician participants will be notified of their patients in the target age group with an upcoming visit who are due for a discussion about CRC screening. The investigators expect that patients seen by clinicians in the intervention arm will report more involvement in the decision making process, be more knowledgeable about the risks and benefits of CRC screening, and will have better quality decisions. Further, the investigators expect that the physicians in the intervention arm will have greater confidence in and demonstrate more skills for conducting shared decision making conversations as compared to those in the control arm.

NCT ID: NCT03244787 Completed - Clinical trials for ColoRectal Cancer Screening

Patient Navigation for Colorectal Cancer Screening for Patients With Mental Illness and/or Substance Use Disorder

Start date: January 2017
Phase: N/A
Study type: Interventional

The investigators propose to develop, implement, and evaluate a novel Colorectal (CRC) screening patient navigator program for patients with Mental Health (MH) and /or Substance Use Disorder (SUD) receiving care at Massachusetts General Hospital Charlestown. The study will involve randomly assigning eligible patients to early intervention or usual care/delayed intervention groups. The investigators believe this random assignment is ethical because Patient Navigation (PN) is an extremely limited resource, and all patients identified as eligible could not be contacted by the navigators in a short period of time. Thus the investigators will randomly assign access to PN during the study period, and then allow all patients to be navigated and screened after the study period is over. As a result, all eligible patients will be referred for PN, but the timing of the referral will be randomly assigned.

NCT ID: NCT03225560 Completed - Colonoscopy Clinical Trials

Smart Phone App for COLOnoscopic PREParation

COLOPREP
Start date: November 21, 2018
Phase: N/A
Study type: Interventional

This is a randomized controlled trial designed to assess the efficacy of a novel smartphone application as an automated reminder tool in improving the quality of bowel preparation for patients undergoing outpatient colonoscopies. The investigators will be comparing the smartphone application to traditional instructions for bowel preparation. The quality of bowel preparation will be assessed using the Ottawa and Aronchick bowel preparation scales.

NCT ID: NCT03208283 Completed - Clinical trials for Colorectal Cancer Screening

Evaluation of the Impact of Water Method During Insertion Phase of Flexible Sigmoidoscopy in Training

FSW
Start date: October 28, 2014
Phase: N/A
Study type: Interventional

Colonoscopy is a sedated procedure traditionally performed using air insufflation during the insertion phase of the procedure. Recently, the use of water method (eg, water infusion or water exchange techniques) during the insertion phase of colonoscopy has been reported to increase the proportion of patients in whom complete unsedated colonoscopy could be achieved, reduce patient recovery time burdens, decrease abdominal discomfort during and after colonoscopy, enhance cecal intubation, and increase willingness to repeat an unsedated colonoscopy. However, there has been no study on the use of water method during the training of primary care doctors or nurse endoscopists in flexible sigmoidoscopy for colorectal cancer screening. In unsedated endoscopic procedure such as FS, endoscope insertion techniques that can potentially reduce patient discomfort and increase the rate of achieving an adequate depth of scope insertion are desirable. Our current study aims to evaluate the impact of water method during insertion phase of FS in the training of primary care doctors or nurse endoscopists for colorectal cancer screening.

NCT ID: NCT03176082 Completed - Colorectal Cancer Clinical Trials

Mailed Reminders Plus Fecal Immunochemical Testing

MFIT
Start date: October 2016
Phase: N/A
Study type: Interventional

Purpose: The investigators propose to test the effectiveness, feasibility, and cost-effectiveness of a mailed reminder with and without FIT kits in a population of Medicaid enrollees in Mecklenburg County.

NCT ID: NCT02754661 Completed - Clinical trials for Colorectal Cancer Screening

Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in the Identification of Colonic Polyps in a Screening Population.

TOPAZ
Start date: September 2016
Phase: N/A
Study type: Interventional

The primary objective of this multicenter, prospective, randomized study is to assess the diagnostic yield of Colon Capsule Endoscopy (CCE) versus Computed Tomographic Colonography (CTC) in a screening population.

NCT ID: NCT02481219 Active, not recruiting - Clinical trials for Colorectal Cancer Screening

Optimization of the Bowel Preparation Regimen for the PillCam COLON 2 Capsule Endoscopy Procedure

Start date: May 2015
Phase: N/A
Study type: Interventional

This study is designed to determine the optimal bowel preparation regimen for PillCam® COLON 2 Capsule Endoscopy System (CCE) procedures in average risk patients. Patients will be randomized to receive one of two bowel preparation regimens prior to PillCam CCE.

NCT ID: NCT02477553 Completed - Clinical trials for Colorectal Cancer Screening

Information With or Without Numbers For Optimizing Reasoning About Medical Decisions

INFORM
Start date: June 2015
Phase: N/A
Study type: Interventional

Experts believe that increasing the low uptake of screening for colorectal cancer (CRC) requires educating patients about all approved tests and helping them choose one that fits their preferences. As one motto puts it: "The best test is the one that gets done." Screening tests range from more invasive and very sensitive for polyps and cancer (colonoscopy) to less invasive and less sensitive (e.g., fecal immunochemical testing (FIT)). But it is unclear how best to educate patients about the options and the tradeoffs involved. Some guidelines recommend that decision aids, a promising tool in this area, provide patients with detailed quantitative information, including baseline risk, risk reduction, and chance of negative outcomes. But this sort of "comparative effectiveness" data can confuse patients, especially those with limited mathematical ability. Previous studies have not measured the effect of providing quantitative information to patients with varying levels of ability or interest or asked them whether such data is essential for their decision-making. The investigators will conduct a clinical trial to determine the impact on patients who view a decision aid (DA) that includes quantitative information versus a DA without such data. The investigators will also seek to determine whether numeracy moderates the effect of quantitative information.