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Injuries clinical trials

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NCT ID: NCT06003504 Active, not recruiting - Emergencies Clinical Trials

The Impact of First Aid Blended Learning Training on Learning Outcomes and Helping Behaviour of Adult Laypeople in Rwanda

Start date: August 7, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to assess the impact of a first aid training delivered through a blended learning approach on learning outcomes and helping behaviour in adult laypeople in Rwanda. Participants will be randomly assigned to either: - a first aid training with blended learning approach; - a first aid training with conventional face-to-face approach; - no first aid training. All participants will be asked before, immediately after, and 6 months after the first aid trainings to complete - a questionnaire on first aid-related knowledge, self-efficacy, and willingness to help; - a practical test on first aid-related skills. The helping behaviour of the participants will be surveyed before and 6 months after the first aid trainings have been completed. Researchers will compare the effects in learning outcomes and helping behaviour after 6 months between: - the first aid training with blended learning approach and no first aid training; - the first aid training with blended learning approach and first aid training with conventional face-to-face approach.

NCT ID: NCT05629156 Active, not recruiting - Injuries Clinical Trials

Injury and Illness Surveillance at the FIFA World Cup Qatar 2022TM

IISFWC22
Start date: November 9, 2022
Phase:
Study type: Observational

The project aims to provide an overview of injury and illnesses during the FIFA World Cup Qatar 2022. All teams are invited to participate and record details on time-loss injury and illness occurrence and training and match exposure during the tournament. In order to assess the severity of injuries (based on the length of time a player is unable to play for), all injuries are to be monitored until they are fully rehabilitated, even if this is after the end of the tournament. This information will be recorded by the team physicians and provided on daily report forms to the research team. Data will be encrypted before analysis and only anonymized data will be published. Descriptive statistics are used to provide an overview of the participant demographics and injury and illness occurrence. Injury incidence is calculated as number of injuries per 1000 hours of exposure, and injury burden is calculated as time-loss days per 1000 hours of exposure. Injury incidence and burden will be reported for training and match injuries separately. Illness incidence is calculated per 365 exposure days.

NCT ID: NCT04469036 Active, not recruiting - Trauma Clinical Trials

Improving Family-Centered Pediatric Trauma Care: The Standard of Care Versus the Virtual Pediatric Trauma Center

Start date: November 30, 2020
Phase: N/A
Study type: Interventional

More than 41 million children, or 55 percent of all children in the United States, live more than 30 minutes away from a pediatric trauma center. The management of pediatric trauma requires medical expertise that is only available at Level I pediatric trauma centers, which are specialized pediatric referral hospitals located in large urban cities. Smaller hospitals lack pediatric trauma expertise and resources to properly care for these children. When a small hospital receives a child with trauma, the standard of care is to conduct a telephone consultation to a pediatric trauma specialist, err on the side of safety, and transfer the child to the regional Level I pediatric trauma center. A newer model of care, the Virtual Pediatric Trauma Center (VPTC), uses live video, or telemedicine, to bring the expertise of a Level I pediatric trauma center virtually to patients at any hospital emergency department. While the VPTC model is being used more frequently, the advantages and disadvantages of these two systems of care remain unknown, particularly with regard to parent/family-centered outcomes. The goal of this study is to optimize the patient and family experience and to minimize distress, healthcare utilization, and out-of-pocket costs following the injury of a child. The results of this project will help to optimize communication, confidence, and shared decision making between parents/families and clinical staff from both the transferring and receiving hospitals.

NCT ID: NCT04129606 Active, not recruiting - Bladder Cancer Clinical Trials

Bladder Perforation Post-TURBT: Definition, Incidence and Natural HistoryStudy

TURBT-BP
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

In view of sparse data of precise definition, risk factors, natural history and management of bladder perforation following Transurethral resection of bladder tumour (TURBT). We aim to correlate the relation between the site, depth and extent of resection with bladder perforation. Also, correlation between vertical depth, horizontal extent of resection and recurrence and progression of tumor

NCT ID: NCT03991806 Active, not recruiting - Frailty Clinical Trials

Association of Centre of Excellence Self- Administered Questionnaire Score and Frailty Levels

Start date: May 31, 2020
Phase:
Study type: Observational

This study evaluates the frailty and the health adverse events in the population of the Canadian Longitudinal Study on Aging. It will be used the Centre of Excellence Self-Administered questionnaire (CESAM) which assesses frailty of older adults by providing a score and a of frailty in 4 levels.

NCT ID: NCT03360539 Active, not recruiting - Preterm Birth Clinical Trials

Nurse-Family Partnership Impact Evaluation in South Carolina

NFP
Start date: April 1, 2016
Phase: N/A
Study type: Interventional

This study evaluates the effects of the Nurse Family Partnership (NFP), an established home-visiting program, using a scientifically rigorous individual-level randomized controlled trial. The study will be based in South Carolina, where a Medicaid waiver in combination with a pay-for-success contract will allow expansion of the program to women on Medicaid. The study plans to enroll 4000 low-income, first time mothers and their children into the intervention group, and another 2000 into the control group. The study will evaluate the program's impacts on outcomes using administrative records. This study aims to yield new evidence on the effect of NFP in a modern context, applied to a new population, across a broad range of outcomes, and financed by a novel public-private partnership based on accountability for outcomes.

NCT ID: NCT03184779 Active, not recruiting - Clinical trials for Knowledge, Attitudes, Practice

The Effect of a Safety Video on Ski and Snowboard School Program Participants in Calgary, Alberta

Start date: July 26, 2016
Phase: N/A
Study type: Interventional

The main objective of the study is to investigate if a video intervention can help increase knowledge, decrease risky behaviours on the hill, and reduce injury risk in students who participate in ski and snowboard school programs. The study design is a cluster randomized controlled trial where participating schools will be randomized into either an intervention or control group. The intervention video will contain an injury prevention and safety promotion component for skiing or snowboarding. The control group will receive the standard orientation video that many schools typically provide for students prior to their ski/snowboard outings in previous years.

NCT ID: NCT00852085 Active, not recruiting - Injuries Clinical Trials

Reducing Youthful Dangerous Driving

RYDD
Start date: October 2005
Phase: Phase 1/Phase 2
Study type: Interventional

To examine the effectiveness of four motivational counseling groups and a directed observational experience in the emergency room in comparison to education and community volunteering only, in reducing high risk driving behaviors