- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03285828
Motivational Interviewing Training for Medical Students: a Pilot Pre-post Study (FEMEM)
Optimising the Relationship Between Medical Students and Patients Through a Motivational Interviewing Training Programme: a Pilot Pre-post Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Design: A pilot pre-post study in 20 students by comparing students' performance before and after MI training session.
Setting: Bicêtre Hospital, Assistance Publique Hôpitaux de Paris, France.
Interventions: Students received three four-hour sessions of a basic MI training over a one week period. The students interviewed for 15 minutes a caregiver playing the role of a patient, six weeks before and three weeks after the training.
Main outcome measures: Global scores by two independent raters who used the Motivational Interviewing Treatment Integrity (MITI) 3.1.1 code, perception of student's empathy by the caregivers (CARE questionnaire), self-efficacy of students to engage in a patient-centred relationship (SEPCQ score), and student's satisfaction with the odds of achieving the target goal.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Students in clinical internships (fourth or fifth year of medical courses) in the Immunology-Infection-Inflammation-Endocrinology Division of Bicêtre Hospital, Assistance Publique Hôpitaux de Paris.
- signed consent
Exclusion Criteria:
- participation refused
- prior training in motivational interviewing
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: First group
Students received three four-hour sessions of a basic motivationnal interviewing training over a one week period.
The students interviewed for 15 minutes a caregiver playing the role of a patient, six weeks before and three weeks after the training.
|
The students received three four-hour sessions of basic motivationnal interviewing training :
|
Other: Second group
Students received three four-hour sessions of a basic motivationnal interviewing training over a one week period.
The students interviewed for 15 minutes a caregiver playing the role of a patient, six weeks before and three weeks after the training.
|
The students received three four-hour sessions of basic motivationnal interviewing training :
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
GLOBAL MITI scores (MITI = Motivational Interviewing Treatment Integrity version 3.1.1)
Time Frame: 15 mn
|
Global scores by two independent raters who used the Motivational Interviewing Treatment Integrity (MITI) 3.1.1
code
|
15 mn
|
perception of student's empathy by the caregivers
Time Frame: 15 mn
|
CARE questionnaire (CARE = The Consultation And Relational Empathy questionnaire)
|
15 mn
|
self-efficacy of students to engage in a patient-centred relationship
Time Frame: 15 mn
|
SEPCQ score (SEPCQ = The self-efficacy in patient-centeredness score)
|
15 mn
|
student's satisfaction with the odds of achieving the target goal.
Time Frame: 15 mn
|
specific questionnary (Analog scale of satisfaction from 1 (not satisfied) to 10 (very statisfied))
|
15 mn
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: ANTOINE CHERET, Bicetre Hospital
Publications and helpful links
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
- FEMEM
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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