Impact of IPE in Multidisciplinary Primary Care Centres on Collaborative Competency of Healthcare Students (FLIRT-MSP) (FLIRT-MSP)

January 17, 2025 updated by: Rennes University Hospital

Impact of Interprofessional Education in Multidisciplinary Primary Care Centres on Collaborative Competency of Healthcare Students - Quasi-experimental Study

The aim of our study is to evaluate the impact of interprofessional education program (IPEP) for healthcare students in clinical placement in MPCC on interprofessional collaboration (IPC), comparing the acquisition of interprofessional collaboration skills in students receiving IPEP during their MPCC placement with those in their MPCC placements without this IPEP.

The IPEP will be delivered by trainers (health professionnals from the MPCC) who receive a train the trainer program.

Study Overview

Status

Not yet recruiting

Detailed Description

For the intervention group, 12 MPCC will be recruited. 3 professionals from each MPCC will be trained and will be responsible for implementing the IPEP for their students.

For the control group, 12 MPCC will be recruited. Students will carry out their clinical placement as usual.

Study method : A multimodal study with a quasi experimental multisite study before and after the IPEP and a qualitative study to explore students' perceptions of the IPC will be conducted.

Study Type

Observational

Enrollment (Estimated)

96

Contacts and Locations

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

Study Contact

Study Contact Backup

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Participants in this study will be :

  • General medicine internship students in Level 1 (7th year) who complete 6-month internships with GPs.
  • Midwifery students doing internships with independent midwives.
  • Occupational therapy students who do internships with occupational therapists in private practice.
  • Pharmacy students (6th year), who complete 6-month internships in community pharmacies.
  • Other students doing clinical placements in MPCCs. A minimum of 48 students are expected to complete internships in MSPs as part of the intervention group.

An equivalent number of at least 48 MSP students in the control group is planned.

Students will be informed of the FLIRT study (intervention and control arms) when they receive the questionnaire, and will agree to take part.

Description

Inclusion Criteria :

MPCC signatories to the interprofessional conventional agreement with the French national health insurance system.

Volunteer to take part in the FLIRT MSP Study. MPCC with GPs who are habilitated to supervise internship family medicine students.

MPCC volunteer to receive healthcare students from different professions including at least one GP intern.

Volunteer to form an interprofessional training team.

Exclusion Criteria:

MPCC who are unable to form an internship training team or to commit to IPE as stipulated in the protocol will not be included in the MSP intervention group.

For the qualitative study, students who do not volunteer or are unavailable for interview will not be included in the FLIRT qualitative component.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
MPCC participating in intervention group
  • MPCC signatories to the interprofessional conventional agreement with the French national health insurance system
  • volunteer to take part in the FLIRT MSP Study
  • volunteer to form an interprofessional training team
  • MPCC with GPs who are habilitated to supervise internship family medicine students
  • MPCC volunteer to receive healthcare students from different professions including at least one GP intern.
The intervention will consist on a train the trainer program. 3 professionals from each MPCC will be trained by an educational team. They will then have to implement an IPEP (knowledge of the MPCC, participation in interprofessional MPCC activities, etc.) for students on placement in their MPCC.
MPCC participating in control group
  • MPCC signatories to the interprofessional conventional agreement with the French national health insurance system
  • volunteer to take part in the FLIRT MSP Study
  • MPCC with GPs who receive internship family medicine students
  • MPCC volunteer to receive healthcare students from different professions including at least one GP intern.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Comparison of changes in student scores on the ICCAS (Interprofessional Collaborative Competency Attainment Survey) before and after the MPCC placement in the intervention and control groups.
Time Frame: 18 months
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of changes in student scores on the ICCAS for each of the 6 IPC dimensions in the intervention and control groups
Time Frame: 18 months
18 months
Comparison of changes in student scores on the ICCAS for each healthcare profession in the intervention and the control groups
Time Frame: 18 months
18 months
Analysis of the experience and feelings of students who have benefited from the IPEP on placement concerning their training and their vision of interprofessional collaboration (qualitative study).
Time Frame: 24 months
The aim will be to understand how the placement changed their view of IPC, how they integrated into the MPCC, how they perceived interprofessional work and how they perceived their professional role within an MPCC.
24 months
Analysis of the feelings of students who did not benefit from IPEP on placement in relation to their education and their view of interprofessional collaboration (qualitative study).
Time Frame: 24 months
The aim will be to understand how the placement changed their view of IPC, how they integrated into the MPCC, how they perceived interprofessional work and how they perceived their professional role within an MPCC.
24 months

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Estimated)

January 1, 2025

Primary Completion (Estimated)

April 1, 2025

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

January 17, 2025

First Submitted That Met QC Criteria

January 17, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 17, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 35RC22_8980_FLIRT-MSP

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plan to make IPD available to other researchers

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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