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Psychological Group Intervention to Reduce Stress and Burnout Among Cardiac Intensive Care Nurses

29 de agosto de 2011 actualizado por: Meir Medical Center

The Contribution of a Short-term Psychological Group Intervention to Reduce Stress and Burnout Among Cardiac Intensive Care Nurses: A Pilot Study

The study will examine the influence of a Cognitive Behavioral Therapy (CBT) short-term group intervention program on the levels of psychological stress and professional exhaustion experienced by the nursing staff in a cardiac department.

Descripción general del estudio

Estado

Desconocido

Condiciones

Descripción detallada

Exhaustion typifies a wide variety of professions, but it is especially evident in the service and aid professions (e.g., teaching and medicine), and nurses in particular are reported to be among the most exhausted. Exhaustion is described as nursing's "professional cancer", and stress is one of the major sources leading to it.

Articles and studies referring to stress among nurses in the years 1980-1996 mapped out six sources of stress stemming from inner sources related to the employee and those stemming from hospital organization: stress that stems from work patterns and overload (such as blurring, lack of clarity, lack of control and coping with death); interpersonal relationships at work (conflicts with other employees and with the medical staff); relationships with patients and their families (insufficient preparation for coping with the emotional needs of patients and their families); work organization and management (for example, lack of staff support and staff shortages); aspects related to the nursing profession (concerns regarding the treatment and care received by the patient), as well as concerns regarding the employee's practical knowledge and skills.

Since stress can lead, among other things, to functional exhaustion and dissatisfaction at work, and since studies have shown that stress has direct and indirect effects on the quality of patient care, it is important to find ways to decrease stress and the resulting exhaustion. Such efforts will increase nurses' efficiency at work and will also improve their quality of life, not to mention that of the patients. Therefore, the current study will examine the effectiveness of a short-term group intervention program for the nursing staff of a hospital's cardiac intensive-care unit.

There are a number of ways to decrease stress which vary both in the theory behind them ( the cognitive approach, for instance, explains the source of stress as stemming from cognitive and behavioral patterns acquired during one's life whereas the dynamic approach relates to deep and unconscious layers of the mind), and in their nature (the way in which they're facilitated). Researchers who have examined the relative efficacy of the different intervention programs in decreasing stress found that cognitive therapy is the most effective approach. Cognitive-behavioral therapy (CBT) can be applied both as individual therapy and as group therapy. According to the researchers, interventions in a group setting have several advantages over individual CBT: creating open relationships between staff members, giving participants an opportunity to get to know one another, providing a platform where employees can express their feelings, developing a sincere support group which proves crucial during stressful work situations, forging a feeling of belonging, and creative solving of shared conflicts and financial issues.

The current study will examine the influence of a CBT short-term group intervention program on the levels of psychological stress and professional exhaustion experienced by the nursing staff in a cardiac department.

The goal of the study:

The current study will examine the effectiveness of a short-term group intervention program for the nursing staff of a hospital's cardiac intensive-care unit. The intervention will include three aspects:

  1. Psycho-educational intervention: attending a lecture about stress and exhaustion.
  2. Techniques for decreasing stress: experiencing relaxation techniques and guided imagery.
  3. A BALINT style group: analyzing actual work cases and cognitive-behavioral focusing for reframing thoughts and making them more adaptive, expressing emotions and training for more appropriate behaviors.

The study, which includes three weekly sessions, assumes that the intervention program will help to significantly decrease the participants' levels of psychological stress and professional exhaustion in comparison with their state before participation in the program, and also in comparison with those who didn't take part in the program (i.e., the control group).

The hypotheses of the study:

  1. Participation in the intervention program will be related to decreased levels of psychological stress. The nursing staff in the program will demonstrate a lower level of negative psychological affect after participation. The level of stress will decrease significantly in comparison with the participants' state in the beginning of the program, and in comparison with professionals who didn't participate in the program (the control group).
  2. Participation in the program will be related to reduced exhaustion levels: the nursing staff members who participate in the program will report lower exhaustion levels than they reported before the program, and in comparison with the control group (members of the nursing staff who didn't participate in the intervention program).

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

24

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.

Estudio Contacto

Copia de seguridad de contactos de estudio

  • Nombre: Noa Vilchinsky, Ph.D
  • Número de teléfono: 972-3-531-8601
  • Correo electrónico: noav18@inter.net.il

Ubicaciones de estudio

      • Kefar Saba, Israel
        • Department of Cardiology, Meir Medical Center
        • Contacto:
        • Contacto:
          • Noa Vilchinsky, Ph.D
          • Número de teléfono: 972-3-531-8601
          • Correo electrónico: noav18@inter.net.il
        • Investigador principal:
          • Morris Mosseri, Professor

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

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Nurses from the cardiac intensive-care unit (CCU) of Meir Hospital, who consent to take part in the offered intervention program

Exclusion Criteria:

  • Refusal to participate

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: Cuidados de apoyo
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Psychological stress and exhaustion
Twenty four male and female nurses from the cardiac intensive-care unit (CCU) of Meir Hospital, who consent to take part in the offered intervention program, will participate in the study. The participants will be randomly assigned to an experiment group of 12 participants and a control group of 12 participants.

The intervention will include three aspects: Psycho-educational intervention: attending a lecture about stress and exhaustion; Techniques for decreasing stress: experiencing relaxation techniques and guided imagery and a BALINT style group:analyzing actual work cases and cognitive-behavioral focusing for reframing thoughts and making them more adaptive, expressing emotions and training for more appropriate behaviors.

The study includes three weekly sessions, Each session will be 90 minutes in duration.

Otros nombres:
  • intervention program
  • short-term group intervention

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Symptoms of psychological stress
Periodo de tiempo: 6 weeks
The Nursing Stress Scale (NSS) has been shown to be a valid and reliable instrument to assess occupational stressors among nurses.
6 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Exhaustion levels
Periodo de tiempo: 6 weeks
Nurse's burnout symptoms: The SMBS questionnaire (Shirom-Melamed Burnout), will be used.This questionnaire reflects the participant's exhaustion in their workplace.
6 weeks

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Morris Mosseri, Professor, Department of Cardiology, Meir Medical Center, Israel

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

1 de agosto de 2011

Finalización primaria (Anticipado)

1 de julio de 2012

Finalización del estudio (Anticipado)

1 de julio de 2012

Fechas de registro del estudio

Enviado por primera vez

2 de mayo de 2011

Primero enviado que cumplió con los criterios de control de calidad

7 de agosto de 2011

Publicado por primera vez (Estimar)

9 de agosto de 2011

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

30 de agosto de 2011

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

29 de agosto de 2011

Última verificación

1 de agosto de 2011

Más información

Términos relacionados con este estudio

Palabras clave

Otros números de identificación del estudio

  • MMC11XXX-XXCTIL

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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