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Screening clinical trials

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NCT ID: NCT01427829 Completed - Screening Clinical Trials

Computer-assisted Psychosocial Risk Assessment (CaPRA) for Refugee Health and Settlement

CaPRA
Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study was to examine preliminary effect of Computer-assisted Psychosocial Risk Assessment tool (CaPRA) among Afghan refugees visiting medical professionals (family physicians or nurse practitioners) at a Community Health Center. The investigators examined the tool's acceptability among patients and its impact on patient satisfaction and patient intention to visit a psychosocial counselor as a proxy of potential to integrate medical and social care.

NCT ID: NCT01375530 Recruiting - Screening Clinical Trials

Screening Volunteers for Clinical Trials

Start date: August 16, 2011
Phase:
Study type: Observational

Background: - The National Institute of Allergy and Infectious Diseases (NIAID) at the National Institutes of Health needs healthy volunteers for vaccine clinical trials. This is a screening study that is used to identify healthy volunteers who may be eligible to participate in other clinical trials at the Vaccine Research Center that evaluate investigational vaccines, monoclonal antibodies, and injection devices. The VRC conducts studies that will allow researchers to better understand the immune system and how vaccines and monoclonal antibodies work. Objectives: - To screen healthy volunteers for clinical trials at the NIAID VRC. Eligibility: - Healthy people between 18 and 60 years of age. They must be available to take part in clinical trials and be able to provide blood for research studies. Design: - Screening for healthy volunteers to participate in clinical trials is an ongoing process. - Volunteers will be asked about their medical history, including sexual activity and drug use, and a detailed physical exam will be performed. - Blood and urine samples may be collected, and possibly other tests as needed to evaluate the volunteer's health status. - Volunteers will not receive any investigational product in this screening protocol....

NCT ID: NCT01183156 Unknown status - Colorectal Cancer Clinical Trials

Re-invitation to Screening Colonoscopy: a Randomized Study

REINVITE
Start date: August 2010
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of reminding letter and educational intervention on attendance to screening colonoscopy in nonresponders to initial invitation to screening colonoscopy.

NCT ID: NCT01182922 Completed - Colorectal Cancer Clinical Trials

Information About a Doctor or a Possibility of Choosing Doctor's Gender and Attendance to Screening Colonoscopy

Start date: August 2010
Phase: Phase 0
Study type: Interventional

The purpose of the study is to investigate whether the information about a doctor or possibility to choose doctor's gender included in invitation letter is associated with attendance rate to screening colonoscopy.

NCT ID: NCT01140022 Completed - Chlamydia Clinical Trials

Leveraging Technology as a Clinician Extender to Screen Culturally Diverse Young Women for Chlamydia

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

The purpose of this study is to conduct a quality improvement intervention to improve the ability of health care providers to deliver an important preventive health service (CT screening) in order to meet the goal of universal CT screening for young women age 25 or younger as recommended by the CDC and virtually all major health organizations. This novel approach utilizes a bilingual (English-Spanish) computer kiosk module to deliver education about CT and allow patients to request a CT screening test. This module should significantly increase CT screening among at risk women (18-25yo) attending urgent care clinics and emergency departments.

NCT ID: NCT00981019 Completed - Screening Clinical Trials

Doctors' Understanding of Survival Statistics

MPIB
Start date: December 2009
Phase: N/A
Study type: Observational

The probably most commonly used measure for expressing the pay-offs of early detection and treatment are survival rates. Yet, over time and groups this metric comes with several biases and thus, is not reliable for judging such benefits. Epidemiologists recommend using reduction of disease-specific mortality rates instead, which is unbiased. The purpose of the study is to investigate how primary care physicians understand and use different survival measures for determining the benefit of cancer screening tests.

NCT ID: NCT00941538 Active, not recruiting - Morality Clinical Trials

Cluster Randomized Controlled Screening Trial for NPC

CRCSTNPC
Start date: January 2008
Phase: N/A
Study type: Interventional

This study is aimed to estimate the effectiveness of an Epstein-Barr virus (EBV) serology-based screening program to reduce nasopharyngeal carcinoma (NPC) mortality in a cluster randomized controlled trial in an NPC high-risk population. Sixteen towns in Sihui and Zhongshan Cities, China will be selected, with eight allocated to the screening group and eight to the control group. Cantonese residents aged 30-69 years with no history of NPC will be included. Residents in the screening towns will be invited to undergo serum EBV VCA/EBNA1 IgA antibody tests.

NCT ID: NCT00582829 Completed - Cancer Clinical Trials

Colorectal Cancer Screening Intervention for Family Members of Colorectal Cancer Patients

Start date: June 2003
Phase: Phase 0
Study type: Observational

This proposed study will use previous study results to guide the development and evaluation of interventions to improve CRC screening acceptance. The proposed study will evaluate the impact of three interventions to promote CRC screening among siblings in this increased-risk group, who are not currently compliant with CRC screening guidelines: 1) a generic print intervention; 2) a tailored print intervention, and; 3) a tailored print plus tailored telephone counseling intervention.

NCT ID: NCT00115557 Completed - Screening Clinical Trials

Delivery of Preventive Services in Primary Care

Start date: October 2004
Phase: N/A
Study type: Interventional

The major goal of this project is to determine the effectiveness of a multi-component intervention designed to help primary care practices implement three office system strategies known to increase delivery of immunizations and other preventive services. This two-year study will contribute to our understanding of multi-component translational interventions in primary care, and particularly within practice-based research networks.