- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01745406
Benefits of the Involvement of Nurses in Meetings Between Physicians and the Families of Patients in the ICU. (NEWS)
When a patient is admitted to the ICU this often happens so suddenly that this can create a significant amount of stress and anxiety for family members for several reasons. Firstly, the family does not have a pre existing relationship with the ICU team. Secondly, the urgency of the situation and the technic it requires is often such that minimal information can be given to family members. And finally, as a result of the unpredictability of each patient's condition, it can be difficult to predict outcome for family members. Together, these factors compound the stress and anxiety of family members. This anxiety is natural and it is important for health caregivers to be able to offer the best support possible. A high quality communication provided by structured information given by physicians and nurses as well could improve support to the families and lead to greater satisfaction.
Giving information to families during meetings is crucial at 3 moments: at the first day when the patient is admitted, at day 3, weekly and each time important news is given (surgery, deterioration in condition, end-of-life).
The purpose of this project is to evaluate if the involvement of nurses during those meetings could improve quality in communication which is assessed by mixed methods. Families and healthcare workers satisfaction will be assessed by qualitative methodology. Family peritraumatic stress, symptoms of anxiety and depression and PTSD will be assessed using validated scales.
Training of healthcare workers will be done by role play. Information to the families is delivered using a framework for physicians and nurses. All the meetings of the study will be audited by a psychologist.
Visão geral do estudo
Status
Descrição detalhada
-Randomized trial with two arms: arm 1: information is delivered by a team (physician and nurse) arm 2: information is delivered by the physician alone
-During the different meetings of the study: at day 1, at day 3, weekly and in case of deterioration of the patient condition.
The other days, family information is delivered as usually in both arms.
Tipo de estudo
Inscrição (Real)
Contactos e Locais
Locais de estudo
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Paris, França, 75014
- Groupe Hospitalier Paris Saint Joseph - Service de Réanimation Polyvalente
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
Inclusion Criteria:
- patient : adult, 1 relative at minimum, mechanically ventilated at least 48 hours; and
- family : french-speaking, adult;
Exclusion Criteria:
- Conflict, organ donor, refusal to participate.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Modelos de observação: Coorte
- Perspectivas de Tempo: Prospectivo
Coortes e Intervenções
Grupo / Coorte |
|---|
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Doctor and nurse
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Doctor without nurse
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Family satisfaction assessed by qualitative approach
Prazo: Patient's ICU discharge day (up to 3 months after Day 1)
|
Patient's ICU discharge day (up to 3 months after Day 1)
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Healthcaregivers' satifaction assessed by qualitative approach
Prazo: End of the study (up to 2 years)
|
End of the study (up to 2 years)
|
Outras medidas de resultado
Medida de resultado |
Prazo |
|---|---|
|
Family PTSD
Prazo: 3 months after patient's ICU discharge (up to 6 months after Day 1)
|
3 months after patient's ICU discharge (up to 6 months after Day 1)
|
|
Family HADS
Prazo: 3 months after patient's ICU discharge (up to 6 months after Day 1)
|
3 months after patient's ICU discharge (up to 6 months after Day 1)
|
|
Family peri-traumatic dissociation
Prazo: Patient's ICU discharge (up to 3 months after Day 1)
|
Patient's ICU discharge (up to 3 months after Day 1)
|
Colaboradores e Investigadores
Patrocinador
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 (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- CPP/107-11
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