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

27 de agosto de 2017 actualizado 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.

Descripción general del estudio

Estado

Desconocido

Condiciones

Intervención / Tratamiento

Descripción detallada

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 estudio

Intervencionista

Inscripción (Anticipado)

18

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Porcelana
    • Hunan
      • Changsha, Hunan, Porcelana, 410005
        • Reclutamiento
        • The First Hospital of Changsha
        • Contacto:
          • Chen Pan, M.D., Ph.D.
          • Número de teléfono: 86-13357319516
          • Correo electrónico: 758933968@qq.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.
Conductual: Mindful Living With Stress
The proposed Mindful Living With Stress Intervention will be conducted weekly, 2 hours per session, 4-6 sessions, group based program in mindfulness.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
stress assessed with a self-administrated questionnaire （Chinese Version of Perceived Stress Scale）
Periodo de tiempo: 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
Periodo de tiempo: 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 resultado secundarias

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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Central South University

Colaboradores

University of California, Los Angeles

Investigadores

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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de enero de 2017

Finalización primaria (Anticipado)

1 de septiembre de 2017

Finalización del estudio (Anticipado)

1 de diciembre de 2017

Fechas de registro del estudio

Enviado por primera vez

13 de octubre de 2016

Primero enviado que cumplió con los criterios de control de calidad

14 de octubre de 2016

Publicado por primera vez (Estimar)

18 de octubre de 2016

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

29 de agosto de 2017

Última actualización enviada que cumplió con los criterios de control de calidad

27 de agosto de 2017

Última verificación

1 de agosto de 2017

Más información

Términos relacionados con este estudio

Palabras clave

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • 16-001305

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

data will be made available within 6 months of study completion

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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