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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01117467
Other study ID # 10/H0501/7
Secondary ID
Status Completed
Phase N/A
First received May 4, 2010
Last updated June 18, 2012
Start date May 2010
Est. completion date December 2010

Study information

Verified date June 2012
Source University of Oxford
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

Simulation is used to teach undergraduate and postgraduate healthcare professionals, however it is not known how best to use this resource. Using qualitative methods, this study aims to investigate how medical students learn during simulation scenarios and will compare students who are paired with peers with those who are solo during their scenarios. Video and audio data from simulations will be collected and analysed with anxiety and empathy questionnaire data and semi-structured interviews.


Description:

Medical students attending a simulation day will either perform their simulation paired with another student from the group or solo. Video data from the scenario and audio data from the feedback session will be retained. One week later students will perform a second scenario and the feedback following this will be retained. Students will also have a semi-structured interview and complete anxiety and empathy questionnaires.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- All final year medical students at the study university who are allocated to attend the anaesthesia special study module

Exclusion Criteria:

- Non-English speakers

- Visiting students who will be unable to complete the study

- Students who refuse to participate

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
Simulation scenario
Students performing their scenario will be paired, not solo
Simulation scenario
Students will perform their simulation scenario solo and receive feedback within the group

Locations

Country Name City State
United Kingdom University of Oxford Oxford Oxfordshire

Sponsors (1)

Lead Sponsor Collaborator
University of Oxford

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Learning during simulation scenario as measured qualitatively 2 years No
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