- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03559998
Learning Process of Fourth Year Medical Students During a Doctor-patient Relationship Training (APTHERA)
Learning Process of Fourth Year Medical Students During an Obligatory Doctor-patient Relationship Training, Including Role Play, Simulated Consultation, Balint Group and Courses: a Mixed Method Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Methodology: Mixed method study with:
Qualitative : Grounded Theory analysis of :
- Semi-structured interview of learners and teachers
- Learning written traces of students
Quantitative features:
- Self-reported questionnaires on satisfaction
- Sociodemographical data and others questions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Paris, France, 75005
- Paris Descartes University, Sorbonne Paris City, Faculty of Medicine
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Undergraduate medical fourth-years student of Paris Descartes University. To diversify recruitment of students for semi-structured interview, investigators will conduct a drawing of lot, thanks to a computer programm, until data saturation.
Apprenticeship trace will also be drawn of lot, until data saturation.
Description
Inclusion Criteria:
- Age > to 18 years old
- Undergraduate medical fourth-year student of Paris Descartes University
- Taking part in an obligatory doctor-patient relationship training, including role play, simulated consultation, Balint group and courses
- Draw by lot
- French or English language
- Agreement
Exclusion Criteria:
- Refusal of agreement
- Undergraduate medical fourth-year student of Paris Descartes University who couldn't take part in an obligatory doctor-patient relationship training, including role play, simulated consultation, Balint group and courses
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Learning processes
Time Frame: 2 hours
|
Learning processes according to students and teachers' perspective evaluated by face-to-face semi-structured interviews, faced with analysis of students' written apprenticeship traces
|
2 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
supporting or preventing factors of learning
Time Frame: 2 hours
|
according to students and teachers' perspective evaluated by face-to-face semi-structured interviews, faced with analysis of students' written apprenticeship traces
|
2 hours
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Marie-Aude PIOT, MD, PhD, Paris Descartes University, France
- Study Chair: Bruno FALISSART, MD, PhD, Paris Saclay South University, Faculty of medicine, Orsay, France
- Study Chair: Antoine TESNIERE, Md, PhD, University of Paris 5 - Rene Descartes
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NI18026HLJ
- 2018-A00385-50 (REGISTRY: ID-RCB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
For data about satisfaction and sociodemographic, it will be collected on a commun and secured base so as to support confrontation of analysis.
For qualitative data, they will be kept on secured informatics interface (of Dr Marie-Aude Piot) of University Hospital Institute "Mutualiste Montsouris". The qualitative researchers will have access to this base for data quotation.
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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