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Prevention Harmful Effects clinical trials

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NCT ID: NCT01896765 Completed - Clinical trials for Myocardial Infarction

Intensive Prevention Program After Myocardial Infarction

IPP
Start date: October 2013
Phase: N/A
Study type: Interventional

It is unknown, if a modern prevention program, including intense nurse-coordinated education sessions, regular telephone contacts and a telephone hotline for 12 months, significantly reduces cardiovascular risk factors, clinical events and quality of life in myocardial infarction patients compared to usual care. Furthermore, actually no data on the additional effects and the feasibility of longterm telemetric care of cardiovascular risk factors exist. The primary hypothesis to be tested is that an intensive longterm prevention program compared to the standard of medical care, will achieve better risk factor control and consecutively less clinical adverse events in patients after myocardial infarctions. The study endpoints will be evaluated after 12 months and during long-term course (after 24 months = one year after termination of the prevention program). In a substudy the effects of short reinterventions ("Prevention Boosts") during long-term course are tested (IPP Prevention Boost Study). Patients with at least one insufficiently controlled risk factor at 24-months visit are randomly assigned to a short (2-month) reintervention vs. no reintervention. The effects of the reinterventions on risk factor control are evaluated after 36 months. A further substudy focusing on young patients <= 45 years of age at time of MI (IPP-Y = IPP in the Young) was added after completion of the pilot IPP study. In this study we focus on the prevention program in young MI-patients. A retrospective analysis of individual genetic risk (assessed by genetic risk scores) in the young patients is included in this substudy.

NCT ID: NCT01707537 Completed - Clinical trials for Prevention Harmful Effects

To Determine the Safety and Immunogenicity of an Oral(Whole Cell) Euvichol Cholera Vaccine in Healthy Adult Men

OCV
Start date: September 2012
Phase: Phase 1
Study type: Interventional

To Determine the Safety and Immunogenicity of an Oral(Whole Cell) Euvichol Cholera Vaccine in Healthy Adult Men

NCT ID: NCT01619202 Completed - Clinical trials for Prevention Harmful Effects

Comparing Driving Performance Among Trained and Untrained Drivers Using a Driving Simulator

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

The purpose of this study is to examine differences in driving performance on a simulated driving assessment between novice teen drivers who receive the Risk Anticipation-Perception Training (RAPT) program and novice teen drivers who do not receive the training program.

NCT ID: NCT01482975 Completed - Clinical trials for Prevention Harmful Effects

Tailored Interventions to Prevent Substance Abuse

Project BEST
Start date: September 2007
Phase: N/A
Study type: Interventional

The overarching objective of this research is to prevent substance use in early adolescents through the use of innovative interactive interventions tailored to each individual's particular risk profile for using cigarettes and alcohol. The specific aims are: (1) To test the effectiveness of the computer-based profile-based tailored interventions to keep early adolescents smoke-free compared to a comparison group; (2) To test the effectiveness of the computer-based profile-based tailored interventions to keep early adolescents from using alcohol compared to a comparison group; and (3) To replicate findings that the tailored diet and physical activity interventions will be effective in reducing these two high risk behaviors as part of the comparison condition.

NCT ID: NCT01310829 Withdrawn - Cancer Clinical Trials

Virtual Reality Intervention in Cancer Genetics

Start date: February 2011
Phase: N/A
Study type: Observational

The goal of this study is to evaluate a virtual reality-based intervention for training health care providers who are not genetics specialists to effectively communicate with and counsel patients regarding cancer genetics.

NCT ID: NCT01195337 Active, not recruiting - Cancer Clinical Trials

Social Contextual Influences on Physical Activity

Start date: August 16, 2010
Phase:
Study type: Observational

The goal of this study is to learn why some black and Latino men and women choose not to exercise very often. Researchers also want to learn more about any social and environmental factors that may affect the way an exercise program is followed.