- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02071420
Efficacy of a Combined Ergonomic Health Promotion Intervention on Employee Health
Descripción general del estudio
Estado
Condiciones
Descripción detallada
Primary Aim: To compare the effects of providing sedentary employees with seated active workstations in combination with an ergonomic intervention and regular motivational emails (experimental group) against the ergonomic intervention and regular emails only (active control group) on occupational sedentary behavior over 16 weeks.
Hypothesis: The addition of a seated active workstation will result in significant reductions in daily occupational sedentary time compared to the active control group.
Secondary Aims: To compare the effects of the experimental group against the active control group on secondary measures of cardiometabolic disease risk factors, musculoskeletal discomfort, cognitive function and work productivity.
Hypothesis 1: The experimental group will result in reduced cardiometabolic disease risk, musculoskeletal discomfort and work limitations compared to the active control group.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Iowa
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Iowa City, Iowa, Estados Unidos, 52242
- University of Iowa
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- We will recruit overweight/obese (body mass index 25.0-40.0 kg/m2) adults (18-65 years) working in full-time (minimum 35 hours/week), sedentary (self-report sitting >75% work time) occupations at an independent work site.
Exclusion Criteria:
- Working in an office that will not meet the space or electrical requirements of the active workstation, acute or chronic illness not under treatment of a provider, orthopedic limitations that prohibit physical activity, current or planned pregnancy, hospitalization from a physical or mental disorder in the past six months and/or taking medication that may impair physical activity
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Experimental Group
This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
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Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.
Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
|
Comparador activo: Active Control
This group will receive the ergonomic intervention and email intervention only for 16 weeks.
This group will not receive a seated active workstation.
|
Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Change in Occupational Physical Activity From Baseline to 16 Weeks
Periodo de tiempo: Baseline and 16 weeks
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Occupational physical activity (primary outcome) will be measured objectively with the GENEActiv physical activity monitor.
The monitor will be worn on the right ankle and will be worn for 5 working days during all non-bathing hours.
The outcome measure will be change in occupational activity (average counts/work day) from baseline to 16 weeks.
The measure will be calculated as follows: 16 weeks value - baseline value.
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Baseline and 16 weeks
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Colaboradores e Investigadores
Patrocinador
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 201306711
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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