Patient safety in coordinated primary care teams: testing a learning system to help MSPs

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study is a multi-method, multi-center, prospective evaluation conducted in the Pays de la Loire region of France. It describes patient safety incidents (PSIs) occurring in MSPs using the PISA classification framework and analyzes how professionals adopt a comprehensive risk-management approach. The project includes a sequential PSI analysis with training of coders, data collection through a web platform, and coding of PSIs by event type, contributing factors, outcomes, and harm severity. It also assesses the implementation of the learning system, including user acceptance, platform usage, and ownership by MSPs. The primary objective is to describe PSI occurrence over 18 months; secondary objectives focus on implementation and uptake of the learning system.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Characteristics of the MSPs included in the study:
* Located in the Pays de la Loire region;
* Having a contract with a health insurance (specifications and financing defined nationally) for at least 1 year;
* Agreeing to take part in the project;
* Having a quality representative or committing to appoint one when they join the project.

Characteristics of professionals working in MSPs included:

* All independent health professionals involved in the MSP: general practitioners and, depending on the MSP, nurses, pharmacists, podiatrists, physiotherapists, midwives, speech therapists, dentists, occupational therapists, psychomotor therapists, etc,)
* All professionals involved in MSP outside the health sector: (coordinators, medical assistants, independent psychologists, etc.),
* agree to take part in the project.

Exclusion Criteria:

Other group exercise modalities or other forms of coordinated exercise (other than MSP) do not have a quality representative on their team and will not be considered for inclusion.

Characteristics of MSPs not included in the research:

\- Where the members of the research team work.

Characteristics of professionals working in MSPs included:

\- Not included.

Where it's running

• Nantes Université
  Nantes, France, France Recruiting

Study contacts

• Study coordinator: Jean-Baptiste Amélineau, MD
• Email: jean-baptiste.amelineau@univ-nantes.fr
• Phone: 02 40 41 28 28

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.