- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02001194
Way to Be Active I (Teams)
A Randomized Trial of Behavioral Economic Interventions to Improve Physical Activities: Team Incentives
Employers are increasingly looking for opportunities to motivate sedentary employees to become more physically active. Workplace walking programs have had mixed success and typically show most improvement among participants that are already fairly active at a baseline. The goal of this study is to determine whether a financial incentive program can motivate sedentary employees to increase the number of steps they walk per day to meet a minimum threshold.
Our primary outcome measure is the proportion of days a minimum activity of 7000 steps or more is achieved. We will assess outcomes each week for 3 months using incentives followed by 3 months of follow-up without incentives. Secondary outcomes will include the average steps walked per day.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- 1. We will use a minimum age of 18 to ensure all individuals are legally able to consent.
- 2. Participant will need an iPhone or Android smartphone to be able to use the Moves App for tracking steps
Exclusion Criteria:
- Conditions that would make participation infeasible: 1a. Inability to consent 1b. Illiteracy and/or inability to speak, read, and write English 1c. Participation in another research study 2. Conditions that would make participation unsafe: 2a. Current treatment for drug or alcohol use 2b. Consumption of at least 5 alcoholic drinks per day 2c. Myocardial infarction or stroke within the past 6 months 2d. Current addiction to prescription medicines or street drugs 2e. Serious psychiatric diagnoses (e.g., severe major depressive disorder, bipolar disorder, schizophrenia) 2f. Pregnant or currently breastfeeding 2g. Metastatic cancer 2h. Unstable medical conditions that would likely prevent the participant from completing the study
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Sin intervención: Control
Participants receive either an email or text message daily (based on the participant's preference) stating whether the participant achieved the 7000 step goal during the previous day.
Each participant will also be notified as to how many of their teammates reached the goal the previous day.
Control Arm will receive no financial incentive.
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Experimental: Individual
Participants receive either an email or text message daily (based on the participant's preference) stating whether the participant achieved the 7000 step goal during the previous day.
Each participant will also be notified as to how many of their teammates reached the goal the previous day.
Every day one team from the arm will be chosen at random as the winning team.
Each participant on the winning team receives $50 if that participant met the step goal during the prior day.
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|
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Experimental: Team
Participants receive either an email or text message daily (based on the participant's preference) stating whether the participant achieved the 7000 step goal during the previous day.
Each participant will also be notified as to how many of their teammates reached the goal the previous day.
Every day one team from the arm will be chosen at random as the winning team.
Each participant on the winning team receives $50 only if all four team members met the step goal during the prior day.
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Experimental: Individual Plus Team
Participants receive either an email or text message daily (based on the participant's preference) stating whether the participant achieved the 7000 step goal during the previous day.
Each participant will also be notified as to how many of their teammates reached the goal the previous day.
Every day one team from the arm will be chosen at random as the winning team.
Each participant on the winning team receives $20 if the participant met the step goal during the prior day the participants met their own goal.
Each participant will also receive an additional $10 for every one of the other three team members that also met the goal.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Proportion of Days a Minimum Activity of 7000 Steps or More is Achieved
Periodo de tiempo: End of study- 6 months of after enrollment
|
Our primary outcome measure is the proportion of days a minimum activity of 7000 steps or more is achieved.
We will assess outcomes for 3 months (13 weeks) with the interventions and 3 months (13 weeks) without intervention during the follow-up period.
We will use all available data and treat missing as true missing data points.
Secondary outcomes will include the average steps walked per day.
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End of study- 6 months of after enrollment
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Average Number of Steps Per Day During Intervention
Periodo de tiempo: End of study- 6 months after enrollment
|
Secondary outcomes include average number of steps per day during intervention period and the follow-up period.
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End of study- 6 months after enrollment
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
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
Palabras clave
Otros números de identificación del estudio
- 819101
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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