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Impact of Narrative Medicine (Workshop Reading Diaries)

Not Applicable
Completed
Conditions
Empathy
Interventions
Behavioral: critical reading
Registration Number
NCT01798290
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Objective: The aim of this study is to assess the impact of an educational program of Narrative Medicine "workshop reading diaries" dedicated to medical students on their empathy.

Design: Randomized Controlled Trial in 2 arms. Participants: Medical students (4th years) of the University Paris Descartes. Methods: participants will be randomized in 2 groups. The allocation of participants will be done by a computerized randomization list, the sequence will be created by an independent statistician. Participants will be blinded of the study hypothesis. Allocation concealment will be provided because only the statistician will have access to the randomization list.

A program of Narrative Medicine with lesson in small group of "workshop reading patients' diaries " vs "workshop reading literature".

Outcome: The primary endpoint will be a first measure of the empathy of the medical students. The secondary endpoints will be a second measure of the empathy of the medical student; satisfaction of the student relative to the educational program .

Potential interests: We believe that the workshop "reading patients' diaries" can develop the thinking of the student with respect to his behavior with the patient, and so the relation between student and patient.

Sample size expected: 200 participants.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
200
Inclusion Criteria
  • All students in the fourth year of medical
Exclusion Criteria
  • refuse to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Behavioral: critical readingcritical readingStudents allocated to the active comparator arm will follow 5 sessions in Class-led instruction of reading literature. They will be divided into eight subgroups of 12 students. The first and fifth sessions will be presential, and 2nd 3rd and 4th sessions will be homework to do on internet.
Primary Outcome Measures
NameTimeMethod
The Jefferson Scale of Physician Empathy5 months after randomization (i.e. 1 month after the end of the intervention)

self-administered questionnaire consisting of 20 items scored by a Likert-type scale (strongly agree = 7, strongly disagree = 1): 10 items are rated positively, others 10 items are rated negatively. The total score ranges from 20 to 140.

Secondary Outcome Measures
NameTimeMethod
The Interpersonal Reactivity Index5 months after randomization (i.e. 1 month after the end of the intervention)

self-administered questionnaire with 4 subscales (Perspective Taking, Empathic Concern, Fantasy, Personal Distress) each containing seven items (a total of 28 items). The items are scored by a Likert scale (0 = Does not describe me well to 4 = Describes me very well).

students' satisfaction4 months after randomization (i.e. 1 month after the end of the intervention)

measure on a numeric scale from 0 (without interest) to 10 (very interesting)

Trial Locations

Locations (1)

Centre d'épidémiologie clinique, Hôtel Dieu

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Paris, France

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