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Mindful Living With Stress for Nurses Caring for HIV/AIDS Patients in China (MLWS)

27 de agosto de 2017 atualizado por: Chen Pan, Central South University

Effect of Mindful Living With Stress (MLWS) Intervention for Nurses Caring for HIV/AIDS Patients in China

The primary objective of this proposed one-year (January 01, 2017 to December 31,2017) project is to assess whether a mindfulness based intervention('Mindful Living With Stress') will be effective at helping nurses caring for HIV/AIDS patients in China to reduce stress. Based on the efficacy of previous studies in stress reduction, it is hypothesized that 'Mindful Living With Stress' will be an effective, feasible and affordable stress reduction program in China.

Visão geral do estudo

Status

Desconhecido

Condições

Descrição detalhada

Background: Considering the great stress in the nurses caring for HIV/AIDS patients, the situation of more serious nursing shortage in China, and the acceptability, feasibility and efficacy of mindfulness-based interventions for reducing stress in health care professionals, here investigators propose a study of "Effect of Mindful Living With Stress (MLWS) Intervention for nurses caring for HIV/AIDS patients in China".

Objectives: The primary objective of this proposed project is to assess whether a program of mindfulness-based stress reduction interventions developed based on Mindfulness Based Stress Reduction (MBSR), Mindful Awareness Practices(MAPs)and chinese culture will be effective at helping nurses caring for HIV/AIDS patients in China to reduce stress and burnout. Based on the efficacy of previous studies in reducing stress, investigators hypothesize that 'Mindful Living With Stress' will be an effective, feasible and affordable stress reduction program for nurses caring for HIV/AIDS patients in China.

Methods: Nurses working in the AIDS department of the First Hospital of Changsha, China will be recruited for the study. The two steps to be implemented include: 1) conducting focus groups with nurses for the purpose of finalizing the design of the MLWS Intervention: A convenience sample of 10 nurses will be recruited and the final sample is expected to include 6-8 participants who will attend two consecutive focus group sessions. The first focus group session will explore the experiences of nurses caring for HIV/AIDS patients and the second focus group session will discuss the design of the MLWS Intervention. The qualitative data will be analyzed after the focus group discussions and the findings will provide important information for development of the final manual for guiding the intervention, and 2) evaluating the effects of the MLWS Intervention in a group of nurses: A convenience sample of 23 nurses will be recruited and the final sample is expected to include 16-18 nurses. The quantitative data from 5 measures assessing stress, burnout, mindfulness, anxiety and depression will be collected and analyzed at pre- and post- intervention. The qualitative data from an in-depth interview will be collected and analyzed at post-intervention.

Implications: The results will provide valuable insights into the effect of MLWS Intervention on stress of nurses caring for HIV/AIDS patients in China. If the MLWS Intervention can be used effectively, it can also be popularized to many other health care professionals caring for HIV/AIDS in China in future.

Tipo de estudo

Intervencional

Inscrição (Antecipado)

18

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

    • Hunan
      • Changsha, Hunan, China, 410005
        • Recrutamento
        • The First Hospital of Changsha
        • Contato:
          • Chen Pan, M.D., Ph.D.
          • Número de telefone: 86-13357319516
          • E-mail: 758933968@qq.com

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

The first step of the study:focus group

Inclusion Criteria:

  1. having a license to practice as a nurse in the People's Republic of China.
  2. being employed as a nurse in the AIDS department of the First Hospital of Changsha for at least 1 year.
  3. Chinese speaking.
  4. being at least 18 years old.

Exclusion Criteria:

  1. being other types of health care providers such as doctors, pharmacists, social workers.
  2. being a nursing supervisor or manager.

The second step of the study: mindfulness intervention

Inclusion Criteria:

  1. having a license to practice as a nurse in the People's Republic of China.
  2. being employed as a nurse in the AIDS department of the First Hospital of Changsha for at least 1 year.
  3. Chinese speaking.
  4. being at least 18 years old.

Exclusion Criteria:

  1. being other types of health care providers such as doctors, pharmacists, social workers.
  2. being a nursing supervisor or manager.
  3. having attended in the focus group of this study.

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: Prevenção
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: mindfulness intervention

The proposed Mindful Living With Stress Intervention will be conducted weekly, 2 hours per session, 4-6 sessions, group based program in mindfulness.The proposed topics include: 1) mindfulness: dealing with stress in a new way, 2) mindful awareness of stress: listening to our body, 3) mindful working with thoughts, 4) mindful working with emotions, 5) mindful interactions, and 6) dealing with obstacles of mindful practices and wrap-up. Mindfulness practices embedded in the program will include mindfulness breathing meditation, sitting meditation, standing meditation, walking meditation, movement meditation (Taichi or Yoga), body scan meditation and daily life meditation.

Data will be collected at pre-intervention (one week before the first session) and post-intervention (one week after the last session) to assess stress, burnout, mindfulness, anxiety,depression,the feedback on the MLWS intervention and the feedback on the influence of MLWS intervention.

The proposed Mindful Living With Stress Intervention will be conducted weekly, 2 hours per session, 4-6 sessions, group based program in mindfulness.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
stress assessed with a self-administrated questionnaire (Chinese Version of Perceived Stress Scale)
Prazo: nine month
At the pre- and post-intervention assessment, participants will complete self-administrated questionnaire on stress.
nine month
stress assessed with an in-depth interview
Prazo: nine month
At the post-intervention assessment,participants will be invited to attend an in-depth interview to give the feedback on the influence of MLWS intervention on living with stress.
nine month

Medidas de resultados secundários

Medida de resultado
Prazo
burnout assessed with a self-administrated questionnaire (Chinese Version of Maslach Burnout Inventory)
Prazo: nine month
nine month
mindfulness assessed with a self-administrated questionnaire (Chinese Version of Five Facets Mindfulness Questionnaire)
Prazo: nine month
nine month
anxiety assessed with a self-administrated questionnaire (State-Trait Anxiety Inventory)
Prazo: nine month
nine month
depression assessed with a self-administrated questionnaire (Beck Depression Inventory)
Prazo: nine month
nine month

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Chen Pan, M.D., Ph.D., Central South University

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 (Real)

1 de janeiro de 2017

Conclusão Primária (Antecipado)

1 de setembro de 2017

Conclusão do estudo (Antecipado)

1 de dezembro de 2017

Datas de inscrição no estudo

Enviado pela primeira vez

13 de outubro de 2016

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de outubro de 2016

Primeira postagem (Estimativa)

18 de outubro de 2016

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de agosto de 2017

Última atualização enviada que atendeu aos critérios de controle de qualidade

27 de agosto de 2017

Última verificação

1 de agosto de 2017

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

data will be made available within 6 months of study completion

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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