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Work Injury Prevention in Law Enforcement Officials

1 de julio de 2015 actualizado por: University of the Pacific

Effectiveness of an Exercise-based Work Injury Prevention Program in Law Enforcement Officials

Law enforcement officials (LEOs) demonstrate an elevated risk for occupational injury. The effectiveness of exercise-based work injury prevention programs (WIPPs) to reduce the risk and costs associated with occupational injury has yet to be tested rigorously in LEOs. The accuracy of existing field tests of physical functioning to predict occupational injuries and related expenses remains unclear. The objectives of this study are to: (i) determine the effect of an exercise-based WIPP on occupational wellness and productivity in a cohort of LEOs, and (ii) to determine the accuracy of 2 common field assessments of physical function to predict lost work productivity and related expenses in a cohort of LEOs.

Descripción general del estudio

Estado

Suspendido

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

108

Fase

  • No aplica

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

    • California
      • Chico, California, Estados Unidos, 95928
        • Butte Premier Physical Therapy
      • Davis, California, Estados Unidos, 95618
        • Physical Edge
      • Lodi, California, Estados Unidos, 95240
        • PUMP Institute
      • Lodi, California, Estados Unidos, 95242
        • Lodi Physical Therapy
      • Stockton, California, Estados Unidos, 95211
        • University of the Pacific

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

18 años a 60 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Age between 18 and 60 years
  • Working full duty as a law enforcement official

Exclusion Criteria:

  • Current history of pathology or symptoms that preclude exercise
  • Medical or rehabilitative treatment for a work-related injury within the past year prior to enrollment in this study

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

  • Propósito principal: Prevención
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Exercise
Exercise will occur 3 times weekly for 6 months in 20-minute exercise sessions. Sessions will take place independently. Follow-up and progression of the home program will be completed in person or by video teleconferencing at regular intervals throughout the intervention phase.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of Work Injury Claims During the Study Period
Periodo de tiempo: One time, at one year following enrollment into the study
One time, at one year following enrollment into the study
Medical Expenditures Related to Work Injury Claims During the Study Period
Periodo de tiempo: One time, at one year following enrollment into the study
One time, at one year following enrollment into the study
Number of Missed Work Days Due to Illness or Injury
Periodo de tiempo: One time, at one year following enrollment into the study
One time, at one year following enrollment into the study
Work Productivity and Activity Impairment Questionnaire - General Health Subscale
Periodo de tiempo: Weekly, up to one year following enrollment into the study
The Work Productivity and Activity Impairment (WPAI) Questionnaire was developed to measure the personal and economic effects of lost workplace productivity in the context of clinical trials. In this study, the WPAI-General Health (GH) version will be used in order to assess lost productivity and wellness during the study period. The WPAI-GH is a 6-item scale that solicits the number of hours missed from work and level of functional impairment perceived at work during the previous week. Four scores are calculated from the WPAI-GH, including percentage of work time missed due to health, percentage impairment while working due to health, percentage activity impairment due to health, an overall percentage work impairment. Time series data will be collected to observe trends over time that may relate to independent variables in this study, as well as to examine for previously unknown and uncontrolled variation (ie, seasonal variability).
Weekly, up to one year following enrollment into the study

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Functional Movement Screen
Periodo de tiempo: One time, at 3 months following enrollment into the study
The purpose of the Functional Movement Screen (FMS) is to provide the clinician with a rapid triage for potentially problematic regions that can contribute to symptoms, disablement, or injury. As a triage tool, FMS is used to determine regions that require additional clinical investigation. The FMS is a battery of 7 tests that are intended as an integrated assessment for limitations in range of motion, weakness, and incoordination. FMS tests consider spine, upper extremity, and lower extremity movements in the context of their respective regional kinetic chain. Component tests of the FMS involve rating of performance by a standardized examiner on a 3-point scale, and specific criteria exist for each rating. A composite score for the FMS may be calculated by summing the item scores.
One time, at 3 months following enrollment into the study
Star Balance Excursion Test
Periodo de tiempo: One time, at 3 months following enrollment into the study
The Star Excursion Balance Test is a clinical test of dynamic balance. Subjects will assume unilateral stance in the center of a grid marked circumferentially in 45-degree increments. After a learning trial consisting of 6 repetitions in each of the 8 test directions, subjects will complete 3 repetitions of single limb squat reach. The evaluating therapist will record the distance achieved between the stance toe and heel of the reaching extremity in each of 3 repetitions in each direction.
One time, at 3 months following enrollment into the study

Colaboradores e Investigadores

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

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

1 de agosto de 2012

Finalización primaria (Anticipado)

1 de diciembre de 2015

Finalización del estudio (Anticipado)

1 de diciembre de 2015

Fechas de registro del estudio

Enviado por primera vez

3 de agosto de 2012

Primero enviado que cumplió con los criterios de control de calidad

11 de junio de 2013

Publicado por primera vez (Estimar)

14 de junio de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

2 de julio de 2015

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

1 de julio de 2015

Última verificación

1 de julio de 2015

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • UPacific_Davenport1

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. .

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