Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

ATI Evidence-based Guide Investigating Medical and Preventative Services

28 de abril de 2026 actualizado por: Natalie Myers, ATI Holdings, LLC

Utilization and Effectiveness of Sports Medicine Services

To use existing standard-of-care documentation in a sports medicine electronic medical record (EMR) to evaluate patient characteristics, interventions delivered, utilization management, and clinical outcomes in routine sports medicine care, in order to generate evidence to improve clinical effectiveness and quality of care.

Descripción general del estudio

Estado

Activo, no reclutando

Condiciones

Descripción detallada

Musculoskeletal (MSK) and sports related injuries are highly prevalent across active and athletic populations and represent a substantial source of healthcare utilization, time loss from participation and a limitation in performance. Often these injuries vary from mechanism, acuity, and severity, ranging from acute traumatic events to chronic overuse conditions. Effective management of these sports-related injuries requires a coordinated effort aimed at helping athletes restore function, minimize the risk of re-injury and facilitating a safe return to sport. Sports Medicine rehabilitation is a widely recognized as a key component of nonoperative care, with evidence that supports the role of athletic trainers to support athletes in improving patient related outcomes, functional performance and return to sport timelines. However, variability does exist in how care is delivered across the sports medicine setting, providers and injury types which may influence both outcomes and resource utilization, underscoring the need to understand how value is achieved within sports medicine rehabilitation.

To address these priorities, investigators from ATI and the University of South Carolina are interested in evaluating how standard-of-care within sports medicine is delivered and how variation in care delivery mechanisms relates to clinical outcomes, value and service utilization. In this retrospective study, The investigators will conduct secondary analyses of existing standard-of-care documentation within ATI's sports medicine EMR, without altering clinical care or interacting with patients. Key variables of interest include: (1) injury and patient characteristics (ie. body region, surgical v. non-surgical status, acuity); (2) functional and performance outcomes (ie. patient reported outcomes, return to sport status); (3) utilization metrics (ie. number of visits, duration of care and frequency); (4) care delivery characteristics (ie. interventions, neuromuscular training, manual therapy and modality use); and delivery care (ie. in clinic, hybrid). By examining how the above variables interact, this study aims to better characterize rehabilitation of athletes receiving sports medicine services and identifying opportunities to optimize outcomes and value.

Investigators have previously used ATI clinical outcomes resources to characterize care patterns, evaluate outcomes and measurement properties, and explore predictors of utilization behaviors such as canceled visits. The present protocol extends this work by leveraging existing standard-of-care EMR documentation to evaluate patient characteristics, interventions delivered, utilization management patterns, and clinical and objective/functional outcomes in routine outpatient care, producing evidence to inform clinical effectiveness, quality improvement, implementation efforts, and policy-relevant value questions.

Tipo de estudio

De observación

Inscripción (Estimado)

550000

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Illinois
      • Downers Grove, Illinois, Estados Unidos, 60515
        • ATI

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

12 años a 25 años (Niño, Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Método de muestreo

Muestra no probabilística

Población de estudio

Individuals receiving medical and/or preventative services when part of an organized sports team.

Descripción

Inclusion Criteria:

Care setting and timeframe: Received sports medicine services at ATI Physical Therapy, with documentation available in the ATI Sports Medicine EMR, on or after January 1, 2018, through the date of data extraction.

Age range: Sports participants including middle school, high school and collegiate aged including adolescents through young adults that have been documented in the EMR.

Record availability: Have an EMR record that includes the minimum data elements necessary to address the study objectives (e.g., episode identifiers/dates sufficient to define an episode of care, diagnosis/body region, utilization variables, and at least one routinely collected outcome measure when applicable to the specific analysis).

Standard-of-care data: Data were collected as part of routine clinical care/documentation prior to and independent of this research study.

Exclusion Criteria:

The record is outside the eligible timeframe or does not reflect sports medicine care at ATI.

The record is a duplicate or cannot be reliably linked within the data source to a single episode/patient for analysis.

The record lacks the minimum necessary variables required for the specific analysis (e.g., missing episode dates needed to define utilization metrics; missing baseline/discharge outcome for analyses requiring change scores).

The data are corrupted, internally inconsistent (e.g., impossible dates), or otherwise unsuitable for analysis after standard data cleaning.

The record cannot be adequately coded/de-identified for analysis and reporting under the study's privacy/confidentiality procedures.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Numerical Rating Scale (NRS)
Periodo de tiempo: Baseline (Day 1 at Evaluation), throughout patient's episode of care asked each visit, on average up to 12 weeks
Subjective; Patients rate pain on a scale from 0 (no pain) to 10 (worst pain imaginable).
Baseline (Day 1 at Evaluation), throughout patient's episode of care asked each visit, on average up to 12 weeks
Single Assessment Numeric Evaluation (SANE)
Periodo de tiempo: Administered at initial evaluation, and every 4th visit for the patient's episode of care (on average 12 weeks).
Subjective, Patient-perceived overall function or pain related to a specific condition compared to pre-injury. 0% (least possible) to 100% (most possible/normal)
Administered at initial evaluation, and every 4th visit for the patient's episode of care (on average 12 weeks).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Silla de estudio: Chris Stout, PsyD, ATI

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • Herring SA. The team physician and return-to-play issues: a consensus statement. Medicine & Science in Sports & Exercise. 2002;34(7):1212-1214.
  • Martin CL, Greene J, David RB, Kliethermes S, Naylor J, Kucera K. Athletic Trainers as Outpatient Rehabilitation Providers: An Analysis of Role, Value, and Insurance Reimbursement in a Large Academic Healthcare System. Journal of Athletic Training. 2025;1(aop)
  • Patel DR, Yamasaki A, Brown K. Epidemiology of sports-related musculoskeletal injuries in young athletes in United States. Translational pediatrics. 2017;6(3):160.
  • Brenner JS, Watson A. Overuse injuries, overtraining, and burnout in young athletes. Pediatrics. 2024;153(2):e2023065129.
  • Coronado VG, Haileyesus T, Cheng TA, et al. Trends in sports-and recreation-related traumatic brain injuries treated in US emergency departments: the National Electronic Injury Surveillance System-All Injury Program (NEISS-AIP) 2001-2012. The Journal of head trauma rehabilitation. 2015;30(3):185-197.
  • Rui P, Ashman JJ, Akinseye A. Emergency department visits for injuries sustained during sports and recreational activities by patients aged 5-24 years, 2010-2016. 2019

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

23 de abril de 2026

Finalización primaria (Estimado)

23 de abril de 2029

Finalización del estudio (Estimado)

23 de abril de 2029

Fechas de registro del estudio

Enviado por primera vez

5 de agosto de 2019

Primero enviado que cumplió con los criterios de control de calidad

7 de agosto de 2019

Publicado por primera vez (Actual)

8 de agosto de 2019

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Descripción del plan IPD

Aggregated non-Private Health Information and non-Health Insurance Portability and Accountability Act data may potentially be made available upon request.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir