- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio 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.
Visão geral do estudo
Status
Condições
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Sem intervenção: 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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|
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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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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Proportion of Days a Minimum Activity of 7000 Steps or More is Achieved
Prazo: 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
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Average Number of Steps Per Day During Intervention
Prazo: End of study- 6 months after enrollment
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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
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- 819101
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
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