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

6 september 2011 bijgewerkt door: 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

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Verwacht)

48

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • London, Verenigd Koninkrijk, SE5 9RJ
        • Institute of Psychiatry, King's College London

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

22 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.
Experimenteel: 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

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in global clinical skills
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in technical clinical skills
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 4 weeks
Post-course feedback questionnaire
4 weeks
Qualitative evaluation
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 augustus 2011

Primaire voltooiing (Verwacht)

1 september 2011

Studie voltooiing (Verwacht)

1 december 2011

Studieregistratiedata

Eerst ingediend

12 augustus 2011

Eerst ingediend dat voldeed aan de QC-criteria

12 augustus 2011

Eerst geplaatst (Schatting)

15 augustus 2011

Updates van studierecords

Laatste update geplaatst (Schatting)

7 september 2011

Laatste update ingediend die voldeed aan QC-criteria

6 september 2011

Laatst geverifieerd

1 augustus 2011

Meer informatie

Termen gerelateerd aan deze studie

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