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- Ensaio Clínico NCT03116451
Nurses' Foot Health and Work Well-being
Nurses' Foot Health and Work Well-being - Development and Testing of an Electronic Foot Health Program
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
An electronic Foot Health Promoting Program (FHPP) will be tested with nurses using quasi-experimental study design.
The participants will be assigned to experimental (N=130) and comparison (N=130) groups. The experimental group will receive an electronic intervention (Foot Health Promotion Program) for 8 weeks consisting of foot self-care guidance (skin and nail self-care), foot exercises, foot stretching and professional footwear guidance. Detailed components of the intervention will be produced on the bases of survey (part 1) results. The intervention (Figure 3) will be electronic via internet (Moodle platform) where a material package of foot health care will be delivered. Each participant will receive a user account to platform. The platform is divided into four main themes all related to foot health. Each theme consists of two topics of foot health. Each topic includes lectures (delivered via Adobe Presenter) and self-directed learning where participant will go through a list of links to websites (will be evaluated with certain criteria beforehand) and watch videos about foot self-care. In addition, the learning will be evaluated using four individual tasks related to foot self-care. By responding to task a participant will receive an example of the correct answer and using that he/she can evaluate own response and learn by that. Participants' use of different links (quantity) and their paths in the intervention platform will be calculated and analysed. The participants will be tested before the intervention (baseline) and one month (follow-up 1) and four (follow-up 2) months after the intervention. The primary outcome is foot health knowledge and secondary outcomes are foot health, musculoskeletal problems, work ability, health-related quality of life and work satisfaction. Hypothesis is: Increasing nurses' knowledge about foot health will improve their foot health and work ability. Ultimate goal is to develop tools for the occupational health care and improve the attention paid to feet as part of the work ability among nurses.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
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Turku, Finlândia, 20520
- University of Turku
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- nurses (registered nurses, licensed practical nurses, public health nurses) working in the operating theatre
Exclusion Criteria:
- other health care professionals
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Experimental: Foot Health Promoting Program
The experimental group will receive an electronic intervention (Foot Health Promotion Program, FHPP) for 8 weeks consisting of foot self-care guidance (skin and nail self-care), foot exercises, foot stretching and professional footwear guidance.
Each topic includes lectures (delivered via Adobe Presenter) and self-directed learning where participant will go through a list of links to websites and watch videos about foot self-care.
In addition, the learning will be evaluated using four individual tasks related to foot self-care.
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An electronic intervention for 8 weeks consisting of foot self-care guidance targeted to nurses.
Outros nomes:
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Sem intervenção: Comparison group
The comparison group will not receive any instructions or guidance for foot self-care but participant in the comparison group will complete the same measurement points than experimental group.
After the study, the comparison group will also receive the same intervention than experimental group (if effective).
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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 from Baseline Foot self-care knowledge at 4 and 12 weeks
Prazo: baseline, 4 weeks, 12 weeks
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Measured with Foot Self-Care Knowledge Questionnaire including 11 questions using a "true," "false," or "don't know" response options.
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baseline, 4 weeks, 12 weeks
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Change from Baseline Foot health at 4 and 12 weeks
Prazo: baseline, 4 weeks, 12 weeks
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Self-reported foot health questionnaire (SFHQ) will be modified for this study.
It will measure self-reported foot health consisting of five subscales: skin, nails, foot structure, foot pain and professional footwear.
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baseline, 4 weeks, 12 weeks
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Change from Baseline Musculoskeletal Disorders at 4 and 12 weeks
Prazo: baseline, 4 weeks, 12 weeks
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Nordic Questionnaire measures musculoskeletal disorders in neck, shoulders, upper back, elbows, low back, wrists/hands, hips/thighs, knees and ankles/feet.
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baseline, 4 weeks, 12 weeks
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Change from Baseline Foot health Status at 4 and 12 weeks
Prazo: baseline, 4 weeks, 12 weeks
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Foot Health Status Questionnaire measures foot health related to quality of life.
There are 4 subscales: foot pain (4 questions), foot function (4 questions), footwear (3 questions), and general foot health (2 questions).
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baseline, 4 weeks, 12 weeks
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Change from Baseline Work Ability Score at 4 and 12 weeks
Prazo: baseline, 4 weeks, 12 weeks
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Work Ability Score, assesses workers self-assessed work ability (one item with 0-10 scale)
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baseline, 4 weeks, 12 weeks
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Minna Stolt, PhD, University of Turku
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
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 (Real)
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
- 116464
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
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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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