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Clinical Research Directory

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2 clinical studies listed.

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Orthopaedic Injuries

Tundra lists 2 Orthopaedic Injuries clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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ACTIVE NOT RECRUITING

NCT07006051

The TCU Division I Collegiate Athlete Study

The overall objective of this study is to identify risk factors for two of the most common types of injuries in collegiate athletics - orthopedic injuries and concussion injuries. Aim 1 of this study is to investigate risk factors for orthopedic injuries from a brief testing battery developed by the research team. Aim 2 of this study is to investigate risk factors for concussion injuries and subsequent sequelae after returning to play from concussion from the same brief testing battery developed by the research team. Additionally, we will examine the relationships between orthopedic injuries and concussion injuries in the collegiate athlete. Participants will participate in a pre-season battery of tests that include: * Balance assessment * Jump testing * Strength testing * Neurocognitive testing Subjects who sustain an injury will undergo repeat testing for comparison to baseline measures. Further, retrospective chart reviews of past medical history and prospective injury tracking will be collected on all subjects.

Gender: All

Ages: 17 Years - 30 Years

Updated: 2025-06-05

1 state

Orthopaedic Injuries
Concussion (Diagnosis)
RECRUITING

NCT06932224

This Study Aims to Measure the Effect of Acute Hospitalisation on the Physical and Cognitive Functioning of Older Orthopaedic Patients (Aged 65 or Above).

This study aims to investigate the impact of hospitalisation on physical and cognitive performance in patients aged 65 and older admitted with an orthopaedic injury. This will be achieved by asking patients to participate in a series of physical and cognitive performance questionnaires and tests. These questionnaires and tests will be performed by the patients as close to their admission as possible and then again at day 7 of hospitalisation (or discharge if earlier) and at 4-6 weeks after discharge. However, if a patient's hospital stay lasts more than 30 days, they will be asked to take part in the interim data collection timepoint. To summarize, patients will be assessed at least 3 times, 4 if your hospital stay is longer than 30 days. The first and second assessments will be in the hospital, and the third will be 4-6 weeks after discharge at you home (or where is appropriate). Additionally, patients will be asked to wear an activity watch between the first and second assessment. The study will also explore patients experiences of their hospital stay and opinions on deconditioning, including the views and opinions of hospital staff. This information will be gathered by having interviews with a sample of the patients who took part in the questionnaires and tests and by having interviews with hospital staff. The interview will be conducted by the main researcher, Thomas Cartledge, and will take place either over the phone, online or in-person, depending on your preference. The interviews will be audio and/or video recorded, however the recordings will be deleted immediately once transcription is completed. The duration of the interview will last approximately 30-60 mins.

Gender: All

Ages: 65 Years - Any

Updated: 2025-04-27

1 state

Deconditioning
Orthopedic Fractures
Hospital Associated Deconditioning
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