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Assessment of a Multifaceted Risk Management Program in French Multiprofessional Offices in Primary Care (PRisM)

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Civil Hospices of Lyon

Status

Completed

Conditions

Patient Safety
Risk Management
Primary Health Care

Treatments

Other: PRisM

Study type

Observational

Funder types

Other

Identifiers

NCT02403388
69HCL14_0265

Details and patient eligibility

About

Avoidable care associated incidents are relatively frequent in primary care. In France for example, avoidable incidents rate is estimated to 22/1000 medical acts from general practitioners. Patient safety is now a growing issue in primary care. One tool to increase patient safety is incident reporting and analysis. It could reduce some important consequences for patients and could allow implementing substantial corrective actions.

The aim of the PRisM study is to assess and compare the efficiency of a multifaceted risk management program implemented in the french pluridisciplinary offices in primary care in association with a centralized incident reporting system, versus a centralized incident reporting system only.

Enrollment

50 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Voluntary multiprofessional primary care offices
  • With at least 10 Full Time Equivalent (FTE)
  • With at least general practitioners and 3 different occupations in care

Exclusion criteria

  • Monoprofessional primary care offices

Trial design

50 participants in 2 patient groups

Multiprofessional primary care offices with PRisM
Description:
25 multiprofessional primary care offices. Each professional of care of the offices (about 10 FTE / office) have to declare each adverse event that occurs in their office during 18 months.
Treatment:
Other: PRisM
Multiprofessional primary care offices without PRisM
Description:
25 multiprofessional primary care offices. Each professional of care of the offices (about 10 FTE / office) have to declare each adverse event that occurs in their office during 18 months.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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