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Participant Satisfaction With Two Different Summative Assessment Methods - a Mixed Method Questionnaire Study

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ClinicalTrials.gov Identifier: NCT03381443
Recruitment Status : Recruiting
First Posted : December 22, 2017
Last Update Posted : July 30, 2019
Sponsor:
Information provided by (Responsible Party):
University Hospital Inselspital, Berne

Brief Summary:
Participants of Immediate Life Support and Advanced Life Support Courses, where two different summative assessment methods were used are asked about their satisfaction with the assessment method using a questionnaire. Both quantitative questions using an 11-point-Likert scale as well as open-ended qualitative questions will be asked. The primary aim of this study is to find out which variant of summative assessment is perceived by course participants as testing their leadership competency best, immediately after the comparison as well as 1 year later to identify any long-term effects on the students.

Condition or disease Intervention/treatment
Assessment Evaluation Other: different assessments

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Study Type : Observational
Estimated Enrollment : 240 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Participant Satisfaction With Two Different Summative Assessment Methods - a Mixed Method Questionnaire Study
Actual Study Start Date : December 2, 2017
Estimated Primary Completion Date : December 30, 2019
Estimated Study Completion Date : December 31, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Health Checkup

Group/Cohort Intervention/treatment
ERC
all students assessed by the methods used by the European Resuscitation Council
Other: different assessments
coded survey about NTS and assessment

AHA
all students assessed by the methods used by the American Heart Association
Other: different assessments
coded survey about NTS and assessment




Primary Outcome Measures :
  1. Participant satisfaction with summative assessment methods during Life Support Courses [ Time Frame: directly after assessment and 1 year later ]
    evaluation of NTS assessed by assessment



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Sampling Method:   Probability Sample
Study Population
All 5th and 6th year medical students at the University of Bern, Switzerland, study year 2017/2018 and 2018/2019
Criteria

Inclusion Criteria:

  • All 5th and 6th year medical students at the University of Bern, Switzerland, study year 2017/2018 and 2018/2019

Exclusion Criteria:

  • Refusal to participate

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03381443


Contacts
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Contact: Sabine Nabecker, M.D. +31 632 3965 sabine.nabecker@insel.ch

Locations
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Switzerland
University of Bern Recruiting
Bern, Switzerland
Contact: Sabine Nabecker, M.D.         
Sponsors and Collaborators
University Hospital Inselspital, Berne
Investigators
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Study Chair: Robert Greif, Prof. University of Bern

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Responsible Party: University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier: NCT03381443     History of Changes
Other Study ID Numbers: ILS_assessment_2017/2018
First Posted: December 22, 2017    Key Record Dates
Last Update Posted: July 30, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No