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Primary Prevention clinical trials

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NCT ID: NCT02984553 Active, not recruiting - Primary Prevention Clinical Trials

Objective Physical Activity Assesment in Postmenopausal Women

Start date: November 2015
Phase: N/A
Study type: Observational

The purpose of this study is to accurately assess weekly physical activity levels of postmenopausal women using lactate thresholds to individualize the accelerometer cut-points.

NCT ID: NCT02653586 Completed - Primary Prevention Clinical Trials

Prevention Program Promoting Self Resilience,Positive Self-Image and Body Image Among Adolescence Aged 15-17

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

The study was a group randomized controlled trial. Within each school Classes of high school students were allocated by randomization to the intervention or control group by a function Randomization in Excel program. Outcomes were measured by questionnaire at pre- intervention, post-intervention and 3-month follow-up. The study protocol was approved by Tel Hai college institutional review board. Parents of all participants, in the intervention and in the control group, received information about the program and the study and were choose whether to provided informed consent or not.

NCT ID: NCT02556112 Completed - Primary Prevention Clinical Trials

Effectiveness of a Group Lifestyle Balance Class in a Military Population

Start date: August 11, 2015
Phase: N/A
Study type: Interventional

With this study researchers will evaluate the effects of the GLB intervention on weight loss, chronic disease indicators and self-perceived function and well-being in an active duty population. The purpose of this study is to examine the effectiveness of the GLB program [compared with two currently available programs, the Fitness Improvement Program (FIP) and the Better Body Better Life (BBBL) program], on the following health indicators: improvement of individual physical fitness as measured by change in abdominal circumference, weight and physical activity; decrease in risk associated with chronic disease as measured by changes in lipid and HbA1c levels; and improvement in self-perceived function and well-being as measured by the RAND 36 Item Short Form Health Survey (RAND SF- 36). In addition, the researchers seek to obtain feedback about the programs from the participants.

NCT ID: NCT02487615 Completed - Primary Prevention Clinical Trials

Genetical, Anthropometrical and Biochemical Factors Influencing High Risk Subclinical Atherosclerosis

Start date: February 2010
Phase: N/A
Study type: Observational

Subclinical atherosclerosis is the atherosclerotic process identified before clinical symptoms and thus it can be a useful marker of future cardiovascular events. It can be evaluated by many methods. This study included the diagnosis of subclincal atherosclerosis by four different methods: coronary calcium score, carotid doppler ultrasound to quantify intima media thickness and carotid plaques, exercise stress test and ankle brachial index. Clinical data, anthropometric measures (body mass index, abdominal circumference), markers of inflammation (high sensitive - C reactive protein, TNF alfa and Lipoprotein Associated Phospholipase A2), fat tissue function (leptin, resistin and adiponectin), glucose metabolism (fasting plasma glucose, glycated hemoglobin and insulin) and genetics markers of atherosclerotic process were evaluated as biomarkers of subclinical atherosclerosis in a uneventful population.

NCT ID: NCT02461238 Completed - Primary Prevention Clinical Trials

Impact of Vouchers and Nutrition Education on the Consumption of Fruits and Vegetables Among Vulnerable Families (FLAM)

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

The purpose of this study is to assess whether fruit and vegetables vouchers combined with educational support may increase fruits and vegetables consumption of children aged 3 to 10 living in vulnerable families in Saint-Denis, France.

NCT ID: NCT01122706 Completed - Stress Clinical Trials

Efficacy of Taiji Training as a Program for Stress Prevention

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

Background: Excessive exposure to psychosocial stress can be a potent trigger for somatic diseases and psychological disorders, a cause for missing work, and eventually lead to high economic loss. Therefore, for health and economic reasons the assessment of effectiveness of stress preventive interventions is of high relevance. According to several clinical studies, Taiji, a Chinese form of mindful and gentle movements, can significantly reduce symptoms of somatic diseases and psychological disorders. Some recently conducted Taiji-studies with healthy subjects indicate a stress protective effect. However, the stress protective impact of Taiji regarding psychosocial stress has not yet been examined. Objective: To investigate the efficacy of a 12 week Taiji training as a stress prevention program by measuring psychosocial stress reactivity in a laboratory setting, as well as the subjective perception of stress and coping-resources in daily life of 70 healthy volunteers. Hypothesis: Healthy subjects attending a 12 week Taiji course (frequency: twice a week for 1h) will show significantly reduced psychobiological reactivity, decreased stress perception and increased coping-resources on a standardized psychosocial stress test compared with healthy subject of the waiting list.

NCT ID: NCT00934206 Completed - Primary Prevention Clinical Trials

Predictors of Individual Training Effectiveness in Preventive Exercise

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

Physical exercise elicits beneficial changes in the body. These concern physical performance but also improvements in virtually all known risk factors for cardiovascular disease. Yet, the extent of individual benefit differs considerably even within homogenous groups and the prediction of individual training effectiveness is not yet possible. This study aims to find predictors of individual training effectiveness.

NCT ID: NCT00619593 Completed - Clinical trials for Sudden Cardiac Death

Survival of Patients With Primary Prophylactic ICD Indication

SPIRIT-ICD
Start date: February 2008
Phase: Phase 4
Study type: Interventional

The MADIT-II trial has shown that patients with severely reduced left ventricular ejection fraction (LVEF) post myocardial infarction benefit from the implantable cardioverter-defibrillator (ICD). However, retrospective analyses of the MADIT-II data have revealed a significantly increased morbidity and mortality in patients with appropriate ICD therapy: Appropriate ICD therapy is associated with 3.3-fold increased all-cause mortality, and the risk of a first heart failure hospitalization is 90% higher after 1st appropriate ICD therapy. Hence, the 1st appropriate therapy might indicate the necessity and utility of further clinical diagnostics and therapy in these patients. This trial is designed to (i) improve the knowledge of the group characteristics of patients suffering from 1st appropriate ICD therapy, (ii) but moreover to take additional therapeutic steps to reduce the mortality of this patient population.

NCT ID: NCT00456911 Completed - Primary Prevention Clinical Trials

Family Dietary Coaching to Improve Nutritional Intakes and Body Weight Control

ELPAS
Start date: March 2005
Phase: N/A
Study type: Interventional

We hypothesize that Family Dietary Coaching for one school year will allow a nutritional shift towards following recommendations and improve health indicators in free-living children and adults.

NCT ID: NCT00213590 Completed - Clinical trials for Kidney Transplantation

Renal Function Evaluation After Reduction of Cyclosporine A Dose in Renal Transplant Patients

DICAM
Start date: April 2000
Phase: Phase 3
Study type: Interventional

The purpose of the study is to show the efficacy of reduction of cyclosporine A exposure measured by the area under the curve by Bayesian estimator on the primary prevention of degradation of the renal function in renal transplant recipients