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Simulation Training vs Workplace-Based Supervision in Psychiatry (EPIC-OSkER)

6 de septiembre de 2011 actualizado por: King's College London

A Randomised Trial of Simulation Training vs Workplace-Based Supervision for Junior Doctors in Psychiatry

The purpose of this study is to evaluate and compare the effectiveness of two forms of clinical skills training for teaching emergency psychiatry skills to doctors who have just started to work in psychiatry

Descripción general del estudio

Descripción detallada

Junior doctors starting work in psychiatry soon encounter a number of situations in the workplace for which they have had little or no preparation either at medical school or from work in other specialities. They will encounter clinically complex situations such as rapid tranquillisation, crisis presentations of self-harm, suicide risk assessment, overseeing supervised confinement and making decisions to admit or discharge mentally ill patients. Furthermore, many of these situations occur out of hours when there is little direct senior supervision available. The traditional induction programme is delivered in a didactic format, which does not encourage effective learning, nor does it allow any opportunity to practise or acquire hands-on skills or non-technical skills such as interprofessional communication, leadership and situational awareness. In the interests of patient safety and improving the quality of care and patient's experience, there is an urgent need to identify ways of improving induction and quickly equipping junior doctors with the clinical skills necessary to practise safely in psychiatry. We propose to evaluate and compare two approached to improved skills training in psychiatry: 1. workplace-based observation and feedback; 2. simulation training.

All new junior doctors starting work in the South London and Maudsley NHS Foundation Trust, London, UK, in August 2011 will be invited to take part in a randomised controlled trial of training in addition to the standard induction. Following a day of lectures on relevant clinical topics, participants will be randomly allocated to receive either observed workplace-based training by a more senior doctor during their on-call duties, or a two-day simulation-based training course. Before and after the training, assessments of participants' clinical skills and attitudes will be carried out by questionnaires and by observations of simulated clinical encounters. Changes in performance will be compared between the two groups. Longer term evaluation will be carried out by means of qualitative interviews and simulated clinical encounters once participants have been working for several months.

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

48

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

      • London, Reino Unido, SE5 9RJ
        • Institute of Psychiatry, King's College London

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

22 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Junior doctors starting work at the South London and Maudsley NHS Foundation Trust in August 2011 in any of the following grades: 1. Core Psychiatric Training; 2. Foundation Training; 3. General Practice Vocational Training; 4. Core Trainee 1-3 equivalent posts, e.g. long-term locums

Exclusion Criteria:

  • Unwillingness to participate in the study
  • Inability to attend the training programme or participate in the evaluation

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

  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: OSkER
"Observed SKills in the Emergency Room" - workplace-based supervision.
For four weeks, participants will be accompanied by a senior psychiatric registrar or consultant psychiatrist, who has received training in giving feedback, during their on-call duties. Each participant will receive between 8-12 hours of 1:1 training.
Experimental: EPIC
"Emergency Psychiatry Immersion Course" - simulation-based training.
A two-day simulation-based training course covering assessment of self-harm, capacity, managing aggression, working with the emergency team and medical emergencies in the psychiatric hospital

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in global clinical skills
Periodo de tiempo: Baseline; 4 weeks; 16 weeks
Participants will participate in a single simulated clinical encounter. Encounters will be video-recorded and then rated by observers, who are blind to the allocation status and time point of each video, using a global rating scale.
Baseline; 4 weeks; 16 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in technical clinical skills
Periodo de tiempo: Baseline; 4 weeks; 16 weeks
Participants will participate in a single simulated clinical encounter. Encounters will be video-recorded and then rated by observers, who are blind to the allocation status and time point of each video, using a checklist-based rating scale.
Baseline; 4 weeks; 16 weeks
Change in attitudes towards teamworking
Periodo de tiempo: Baseline; 4 weeks; 16 weeks
The Operating Room Management Attitudes Questionnaire will be modified to be appropriate for working in psychiatry.
Baseline; 4 weeks; 16 weeks
Change in attitudes towards self-harm
Periodo de tiempo: Baseline; 4 weeks; 16 weeks
The Attitudes to Deliberate Self-Harm Questionnaire
Baseline; 4 weeks; 16 weeks
Self-reported views on usefulness and acceptability of the training programmes
Periodo de tiempo: 4 weeks
Post-course feedback questionnaire
4 weeks
Qualitative evaluation
Periodo de tiempo: 8 - 12 weeks
Focus groups will be conducted to evaluate how participants have learned to manage psychiatric emergencies, and the contribution of the courses to their learning.
8 - 12 weeks

Colaboradores e Investigadores

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

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 septiembre de 2011

Finalización del estudio (Anticipado)

1 de diciembre de 2011

Fechas de registro del estudio

Enviado por primera vez

12 de agosto de 2011

Primero enviado que cumplió con los criterios de control de calidad

12 de agosto de 2011

Publicado por primera vez (Estimar)

15 de agosto de 2011

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

7 de septiembre de 2011

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

6 de septiembre de 2011

Última verificación

1 de agosto de 2011

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2011/051

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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