Learning Process of Fourth Year Medical Students During a Doctor-patient Relationship Training (APTHERA)

April 16, 2021 updated by: Assistance Publique - Hôpitaux de Paris

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

This study aims to explore learning process for undergraduate students in this doctor-patient relationship course. This study is one of the 3 studies included in a PhD on learning process during simulation training in psychiatry. The results of this 3 studies will aim at building a formative and summative assessment tool of competences specific to this pedagogic context.

Study Overview

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

Observational

Enrollment (Actual)

404

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Paris, France, 75005
        • Paris Descartes University, Sorbonne Paris City, Faculty of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

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

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

June 2, 2018

Primary Completion (ACTUAL)

June 30, 2018

Study Completion (ACTUAL)

June 30, 2018

Study Registration Dates

First Submitted

June 6, 2018

First Submitted That Met QC Criteria

June 6, 2018

First Posted (ACTUAL)

June 18, 2018

Study Record Updates

Last Update Posted (ACTUAL)

April 19, 2021

Last Update Submitted That Met QC Criteria

April 16, 2021

Last Verified

April 1, 2021

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)?

YES

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

From data collection (june-july 2018 to data saturation estimated at December 2018)

IPD Sharing Access Criteria

Only researchers involved in data analysis

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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