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Injury clinical trials

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NCT ID: NCT01993056 Completed - Injury Clinical Trials

The Influence of 11+ on Injury Incidence and FMS-Score in Veteran Soccer Players

Start date: August 2011
Phase: N/A
Study type: Interventional

According to available data the injury rate in male veteran soccer is high. Interventions to prevent injuries are requested. The 11+ warm-up program was developed by FIFA-experts and consists of several exercises with an overall-length of about 20 min. This study shall investigate the influence of 11+ on injury incidence and Functional Movement Screen (FMS)-Score in male veteran soccer players. Additionally it is to be examined if there is a relationship between FMS-Score and injury incidence. For this purpose the 11+-program is accomplished under supervised conditions over one regular season in a randomized-controlled study design. Injuries are documented via questionnaires in accordance with the FIFA-consensus-statement. FMS-Score is evaluated before and after the interventional period.

NCT ID: NCT01459978 Completed - Injury Clinical Trials

Impact of Monitoring Quality Indicators in Maternity Departments on Mother and Infant Health

MATICUS
Start date: September 2012
Phase: N/A
Study type: Observational

Hypothesis: Continuously monitor quality indicators with a specific method (CUSUM: Cumulative Sum) will increase the awareness of health care staff in maternity and permit rapid detection of a small dip in performance in order to enable prompt investigations and corrective measures when necessary , which decrease maternal and neonatal mortality and morbidity. Objective: To assess the impact of Cumulative Sum (CUSUM) charts used as a maternity dashboard to decreases maternal and neonatal mortality and morbidity. Design: Step-wedge cluster-randomized trial with prospective analyses of collected data. Setting: ten Maternity departments in France. Population: Data from 60 000 women and infants could be collected over 2 year's period. Method: Cumulative sum (CUSUM) charts were used to monitor the rate of quality indicators previously selected by Delphi method. Main Outcome Measures: Composite outcome that considers multiple clinical events : mortality, adverse outcomes for women and newborn.

NCT ID: NCT01444170 Completed - Inflammation Clinical Trials

Nutritional Supplement, Eccentric Exercise and Recovery

Start date: July 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The objectives of this study are to assess the effectiveness of a nutritional supplement on muscle functional recovery following induced muscle damage from high intensity resistance exercise. The investigators hypothesize that a short-term dietary supplementation will significantly improve muscle functional recovery following an intense bout of eccentric exercise compared to a placebo.

NCT ID: NCT01148784 Completed - Injury Clinical Trials

Comparison of Doubled Quadrupled Versus Quadrupled Allograft Tissue Constructs for Anterior Cruciate Ligament (ACL) Reconstruction

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

The purpose of this study is to compare two different soft tissue allografts, double bundle tibialis anterior allograft or quadruple bundle hamstring allograft, used in repairing a torn anterior cruciate ligament (ACL) of the knee.

NCT ID: NCT01084590 Completed - Obesity Clinical Trials

Healthy Homes/Healthy Kids_5-9

HHHK_5-9
Start date: March 2010
Phase: N/A
Study type: Interventional

The pediatric primary care setting is a relatively untapped resource for addressing obesity prevention. The main goal of this study is to evaluate the efficacy of a relatively low cost pediatric primary-care based obesity prevention intervention. The intervention will consist of brief pediatrician counseling as well as phone coaching for parents with overweight children who are between the ages of five and nine. We propose to enroll and randomize 425 parent-child dyads with children who have a measured body mass index (BMI) the 75th and 95th percentile. They will be randomized one of into two groups, the (a) Healthy Eating/Physical Activity Intervention, or the (b) General Healthy/Safety/Injury Prevention Contact Control Intervention. Both groups will receive brief pediatrician counseling regarding their child's current BMI percentile status and recommendations for home environmental changes to achieve a healthy weight gain trajectory and to improve home safety and reduce injury risk. This will be paired with a 12 month home-based program delivered via phone by health behavior specialists to help parents make environmental changes specific to their group assignment.

NCT ID: NCT01044953 Completed - Injury Clinical Trials

Injury Incidence in Professional Soccer

Start date: January 2009
Phase: N/A
Study type: Observational

The winter break within the German Professional Football Leagues will be shortened as for the season 2009/2010 from 6.5 to 3.5 weeks. That might have repercussions on injury incidence in either way, positive or negative. On the one hand, recovery time during the winter will be shorter, which might lead to an increased risk of injury. On the other hand, it will allow a better spread of games in the second round, thus reducing the amount of the so-called "English weeks", which in turn could reduce the number of injuries. This study compares injury incidence between the season 2008/2009 (long winter break) and the season 2009/2010(short winter break) via questionnaires in accordance with UEFA/FIFA injury evaluation criteria.

NCT ID: NCT01027104 Completed - Training Clinical Trials

Evaluation of a Resident Curriculum in Firearm Injury Prevention

Start date: December 2007
Phase: N/A
Study type: Interventional

The purpose of this project is to evaluate the efficacy of a web-based curriculum designed to teach pediatric practitioners how to provide injury prevention anticipatory guidance, emphasizing firearm injury prevention in a clinic setting. Data will be collected regarding the curriculum's effectiveness using a web-based questionnaire which will be administered to pediatric residents prior to, immediately post, and six months following completion of the curriculum. Pre- and post-test questionnaires will be compared. Residents will also be asked to evaluate the curriculum by completing a survey. We hypothesize that the curriculum will improve residents' knowledge, attitudes and beliefs, and self-efficacy regarding firearm injury prevention anticipatory guidance.

NCT ID: NCT00935428 Completed - Injury Clinical Trials

Causes and Circumstances of Horse Related Injuries and Impact on Quality of Life

Start date: June 2009
Phase:
Study type: Observational

Horse-related activity can be risky. Horses are the leading cause of animal-related fatalities in Oregon and Oregon's annual death rate from animals is 45% higher than the national rate. By interviewing injured equestrians, the investigators may be able to determine patterns of decision-making and behavior from their collective experience and develop useful safety recommendations. The investigators will also determine the impact that the injury has had on quality of life. The long-term goal of the investigators research is to develop safety and prevention recommendations and a horse-related injury prevention program to reduce the number of horse related injuries.

NCT ID: NCT00920049 Completed - Injury Clinical Trials

Preventing Motor Vehicle Crashes Among Young Drivers: Evaluation of the Checkpoints Program Presented by the American Automobile Association

Start date: June 5, 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Background: - Automobile crash risks are highest right after licensure and decline rapidly for about 6 months and then gradually for years, regardless of the amount of supervised practice driving or age at licensure. The only approaches to this problem that have demonstrated effectiveness are Graduated Driver Licensing (GDL) and parental management. - The Checkpoints Program consists of persuasive messages and materials designed to increase adoption of the Checkpoints Parent-Teen Driving Agreement and to improve parents' ability to set limits on higher-risk driving privileges for novice drivers. Researchers are interested in determining whether expanding the Checkpoints Program to an online version (instead of through the mail) can help improve parent limit-setting in connection with the program. Objectives: - To determine the feasibility and effectiveness of conducting an online version of the Checkpoints Program through American Automobile Association (AAA) clubs. - To test rates of parental intervention and limit-setting after participation in the Checkpoints Program. Eligibility: - Parents whose teenage children are enrolled in AAA-affiliated driving schools. Design: - Parents with children at the permit stage of driver's education will be recruited through AAA clubs and will be asked to visit a designated Web site to sign up for the program. - Parents will provide consent and complete the baseline survey, and will be assigned to random groups to test different versions of the Checkpoints Program (the intervention or a control group Web site). - The intervention program will contain videos, regular e-mails, and newsletters on setting parental limits and information on specific teen driving risks. The control program will provide information on various topics related to the licensing procedure and safe driving, but no specific information on teen driving risks. - A follow-up assessment will be conducted 1 month after the teenager receives his or her license.

NCT ID: NCT00738504 Completed - Injury Clinical Trials

Intensive Insulin Therapy and Acute Kidney Injury. Analysis Using RIFLE Criteria.

Start date: June 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine if intensive insulin therapy really reduces the incidence of acute kidney injury in critically ill patients, using for analysis the RIFLE criteria for definition of AKI.