Access to a Sit-stand Computer Workstation and Back Pain
6 de outubro de 2017 atualizado por: Kathleen Horst, Stanford University
Evaluating Change in Back Pain From Access to a Sit-stand Workstation
The purpose of the study is to evaluate the changes in back pain from access to a sit-stand workstation.
Other muscle and joint pain and/or discomfort will also be evaluated.
We hypothesize that access to a sit-stand workstation will allow one to experience postural variation and reduce back pain.
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Real)
57
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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California
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Stanford, California, Estados Unidos, 94305
- Stanford University
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
18 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
- Back pain lasting ≥3 months and reported at a minimum of 4 out of 10 on the pain scale.
- Sits >6 hours out of an 8-hour work day for work purposes
- Able and willing to fill out a daily survey for the first week prior to randomization
- Participants must be >18 years of age. There are no gender/race-ethnic restrictions.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Unable to stand for at least 10 minutes.
- Currently using a sit-stand desk
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Sem intervenção: Control
Did not receive an intervention during the active portion of the study (i.e. 12 weeks).
After the active portion of the study, this group was given a sit-stand computer workstation.
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Experimental: Sit-stand computer workstation
Given a sit-stand computer workstation to use at their place of work
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A sit-stand computer workstation allows one to sit or stand throughout the day while maintaining continued use of one's computer.
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
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Change in Back Pain
Prazo: Baseline (Week 1) and Follow-Up (Week 18)
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The Roland-Morris Disability Questionnaire is designed to assess self-rated physical disability caused by low back pain.
The patient is asked to agree or disagree with 24 different statements related to their back pain.
The end score is the sum of the agreed statements.
The score ranges from 0 (no disability) to 24 (maximum disability).
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Baseline (Week 1) and Follow-Up (Week 18)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Pain in Other Body Parts
Prazo: At the conclusion of each work day for 12 weeks and 8 weeks later
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The Brief Pain Inventory (BPI) allows patients to rate the severity of their pain and the degree to which their pain interferes with common dimensions of feeling and function.
This data was not analyzed due to the focus of the project on lower back pain.
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At the conclusion of each work day for 12 weeks and 8 weeks later
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Kathleen C Horst, MD, Stanford University
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
Publicações Gerais
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Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo
1 de abril de 2013
Conclusão Primária (Real)
1 de dezembro de 2013
Conclusão do estudo (Real)
1 de março de 2014
Datas de inscrição no estudo
Enviado pela primeira vez
21 de maio de 2014
Enviado pela primeira vez que atendeu aos critérios de CQ
21 de maio de 2014
Primeira postagem (Estimativa)
23 de maio de 2014
Atualizações de registro de estudo
Última Atualização Postada (Real)
6 de novembro de 2017
Última atualização enviada que atendeu aos critérios de controle de qualidade
6 de outubro de 2017
Última verificação
1 de outubro de 2017
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- SSCWStanford
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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