Injuries

9

Review clinical trials related to Injuries. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Medical Team Perspectives on Hand and Wrist Injuries in Elite Male and Female Ice Hockey Players

This is a cross-sectional survey study investigating how medical team staff in elite Swedish ice hockey perceive hand and wrist injuries in male and female players. Hand and wrist injuries are common in ice hockey and can affect both performance and participation. While injury registries describe how often these injuries occur, less is known about how they are managed and prioritised in daily clinical practice, or whether there are differences in perception between medical teams working in male and female elite leagues. In this study, physiotherapists and team physicians working in Swedish elite ice hockey (including SHL, HockeyAllsvenskan, and SDHL) will complete a structured questionnaire. The survey examines perceptions of injury frequency, underreporting, functional impact, clinical management strategies, and return-to-play decision-making related to hand and wrist injuries. The aim is to better understand how medical teams experience and manage these injuries in real-world elite sport settings, and to identify potential gaps between epidemiological data and clinical practice. The study may help inform future injury prevention strategies, improve clinical decision-making, and support the development of more standardized management approaches in elite ice hockey. No interventions or treatments are performed in this study.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dalarna County Council, SwedenUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Physiotherapists working with elite ice hockey teams in Sweden (SHL, HockeyAllsv... [+5]

Refusal to participate [+1]

Status: Recruiting

Driver Education Research Study

This study will test the effectiveness of different types of driver training interventions for reducing young new driver crash risk early after licensure.

Participants needed: 1,300
Trial details
Age: 16-17Biological sex: AllType: InterventionalSponsor: Children's Hospital of PhiladelphiaUpdated: Apr 6, 2026Locations: 1
Eligibility criteria

Adolescents ages 16-17 years old who reside in Pennsylvania [+10]

Non-Pennsylvania resident [+2]

Status: Recruiting

The Mother in Norway Study

The Norwegian government is implementing the Nurse Family Partnership program (NFP) to combat child abuse and social inequality. This study will examine NFP with an individually randomized controlled parallel-group trial. The study will enroll 700 mothers over three years, with half receiving NFP services and the other half receiving standard care. The primary outcome is violence towards mothers and their children, assessed through questionnaires and observation tests. The study will also evaluate the program's effects on various health-related outcomes using administrative data. Cost-effectiveness analyses will be conducted to compare NFP to existing services and improve its delivery efficiency.

Participants needed: 700
Trial details
Age: 16+Biological sex: FemaleType: InterventionalSponsor: Oslo Metropolitan UniversityUpdated: Aug 11, 2025Locations: 5
Eligibility criteria

Not listed

Status: Recruiting

Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents

Generation Victoria (GenV) is a longitudinal, population-based study of Victorian children and their parents that will bring together data on a wide range of conditions ,exposures and outcomes. GenV blends study-collected, study-enhanced and linked data. It will be multi-purpose, supporting observational, interventional, health services and policy research within the same cohort. It is designed to address physical, mental and social issues experienced during childhood, as well as the antecedents of a wide range of diseases of ageing. It seeks to generate translatable evidence (prediction, prevention, treatments, services) to improve future wellbeing and reduce the future disease burden of children and adults. The GenV Cohort 2020s is open to all children born over a two-year period, and their parents, residing in the state of Victoria Australia. The GenV Cohort 2020s is preceded by an Advance Cohort of children born between 5 Dec 2020 and 3 October 2021, and their parents. This comprises all families recruited at GenV's Vanguard hospital (Joan Kirner Women's and Children's) and at birthing hospitals throughout Victoria as GenV scaled up to commence recruiting for the GenV Cohort 2020s. The Advance Cohort have ongoing and full participation in GenV for their lifetime unless they withdraw but may have less complete data and biosamples.

Participants needed: 150,000
Trial details
Age: 1+Biological sex: AllType: ObservationalSponsor: Murdoch Childrens Research InstituteUpdated: Aug 3, 2025Locations: 1
Eligibility criteria

Birth date between 4th October 2021 and 3rd October 2023 [+5]

Children who are deceased at the time of recruitment (i.e. still born or died af... [+1]

Status: Recruiting

Arabic Version of Marx Activity Rating and Knee Stability in Sports/Cutting-Pivoting Ability Scales

Anterior cruciate ligament (ACL) injuries are among the most common knee ligament injuries, causing joint instability and impairments. Besides being challenging, this type of injury greatly affects the athlete's passion and wellbeing, and it is associated with several risk factors. Injuries to the ACL are estimated to occur within 80,000 to 250,000 young, active and healthy athletes each year. This cross-sectional observational study aimed at translating, adapting cross-culturally, and investigating the psychometric properties of the Marx Activity Rating Scale (MARS) and the Knee Stability in Sports/Cutting-Pivoting Ability (KSS/CPA) scale in Saudi patients with anterior cruciate ligament injuries. For this study, a convenient sample size of 100 athletes with ACL injuries and healthy participants will be selected from different Saudi hospitals and clubs. Study participants will be informed about the study and a consent form will be obtained before they participate. A number of scales will be used as outcome measures, including the MARS, KSS/CPA scale, Knee Injury, and Osteoarthritis Outcome Score, Lysholm Knee Score, and International Knee Documentation Committee Subjective Knee Form. Internal consistency of both the MARS and KSS/CPA scales will be tested using Cronbach's alpha. A construct's validity will be measured by Spearman's correlation coefficient. Content validity can be determined by examining whether there are floor and ceiling effects. A significance level of 0.05 will be used to determine whether the data is significant. Ultimately, the study will help patients with ACL injuries to make informed decisions about their treatment, empower healthcare professionals to understand patients' concerns, and facilitate research.

Participants needed: 150
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Imam Abdulrahman Bin Faisal UniversityUpdated: May 14, 2025Locations: 1
Eligibility criteria

An athlete with an orthopedic diagnosis of unilateral ACL injury [+3]

1 Patients with other lower limbs or different musculoskeletal injuries such as...

Status: Not yet recruiting

A Study of Child Injury Based on Data Mining

A comprehensive pediatric injury burden assessment is an essential foundation for formulating injury prevention strategies and improving emergency care for injured children. Although the hospital-based passive surveillance of national injury surveillance system of medical and health institutions has been well-established in China, the monitoring points of hospitals were not stratified according to children's hospital. Aim of the project is to collect epidemiological and clinical data to describe causes, clinical features and outcomes of pediatric injuries at a Children's Hospital in Shanghai, China. The project intends to establish a method for collecting and analyzing high quality data of child injury using data mining based on the hospital information system.

Participants needed: 10,762
Trial details
Age: 0-18Biological sex: AllType: ObservationalSponsor: Children's Hospital of Fudan UniversityUpdated: Feb 18, 2025
Eligibility criteria

Not listed

Status: Recruiting

Characteristics of Injury Claims by Chronic Pain Patients

Chronic pain is associated with injuries and disabilities. This prospective observational study explores the injury or disability claims made by chronic pain patients. It evaluates the socio-demographics of the patient population. It explores the impact of pain clinic services on the patients' injury rehabilitation, insurance claim outcome, and socioeconomic situation.

Participants needed: 1,000
Trial details
Age: 20-99Biological sex: AllType: ObservationalSponsor: Salem Anaesthesia Pain ClinicUpdated: Jan 27, 2025Locations: 1
Eligibility criteria

adult chronic pain patients [+1]

pediatric patients [+1]

Status: Not yet recruiting

The Safety Integration Stakeholders (SAINTS) Program to Integrate Worker and Patient Safety in Oregon Rural Hospitals

The safety integration stakeholders (saints) program to integrate worker and patient safety in Oregon rural hospitals. The rationale is that the saints program will positively impact outcomes by identifying and training peer leaders on strategies to optimize environmental, administrative, and educational components to become a saint and regularly collaborate with safety stakeholders/administrative leaders at each site through continuous improvement cycles (e.g. plan-do-study-act).

Participants needed: 240
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Mar 22, 2024
Eligibility criteria

Employed at participating sites (critical-access hospitals in rural Oregon) [+1]

Non-clinical staff (e.g. clerical, janitorial) [+1]

Status: Recruiting

Prospective Urban Rural Epidemiology Study

To examine the impact of health determinants at the individual (e.g. health related behaviors) and societal level (e.g. environmental factors, health related policy, quality of health systems) on health outcomes (e.g. death, non-communicable disease development) across a range of socioeconomic and health resource settings. Additional components of this study will examine genetic factors for non-communicable diseases. This will be examined both through a cross sectional component, and prospectively (cohort component).

Participants needed: 200,000
Trial details
Age: 35-70Biological sex: AllType: ObservationalSponsor: Population Health Research InstituteUpdated: Jan 31, 2024Locations: 34
Eligibility criteria

consenting adults between 35-70 years of age

none