Health Care Appropriateness Assessment and Support Programme at a University Hospital Centre (CHU) in Bordeaux

NCT ID: NCT04908501

Last Updated: 2023-02-24

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 6 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-10-07
• Study Completion Date: 2023-06-30

Brief Summary

Non-appropriateness of care is a common and serious phenomenon that affects healthcare institutions in France. Appropriateness in health care is about adequacy of any type of health care with patient's needs. Relying on structuring innovative tools, the hospital university centre of Bordeaux is implementing a health care appropriateness assessment and support programme ("sPREAd pertinence").

By using a mixed method, the project's main objective is to evaluate programme effectiveness on the improvement of care appropriateness in hospital university centre of Bordeaux. Other assessments are considering impact on: specific care appropriateness indicators, care related adverse events frequency, organizational climate, and work life satisfaction. The economic impact of this program in terms of induced costs and avoided costs will be evaluated. A qualitative approach will be used to identify the programme transferability conditions with a view to produce an Operational Model for the Implementation of Appropriateness at a Healthcare Institution.

Detailed Description

Non-appropriateness of care is a common and serious phenomenon that affects healthcare institutions in France. Appropriateness in health care is about adequacy of any type of health care with patient's needs. It means that a health care is necessary and relevant, given a specific indication, with regard to updated practice recommendations or justifications of experts.

The hospital university centre of Bordeaux is making Health care appropriateness a policy priority. Relying on structuring innovative tools, it is implementing a health care appropriateness assessment and support programme ("sPREAd pertinence"). This programme comprises two parts, one regarding interventional aspects and the other concerning assessments.

sPREAd-Pertinence programme's objectives Project's primary objective is to evaluate programme effectiveness on the improvement of care appropriateness in hospital university centre of Bordeaux.

Project's secondary objectives are :

• to assess impact on specific care appropriateness indicators, care related adverse events frequency, organizational climate and work life satisfaction.
• to evaluate the actual use of GAP.
• to measure the costs of implementing the sPREAD Perti program and to identify the additional costs incurred in comparison with the mobilization and support approach to care appropriateness already existing at the Bordeaux University Hospital;
• to compare the costs of the program with the consequences observed in terms of specific care appropriateness improvement, changes in serious adverse events frequency, organizational work climate and work life satisfaction;
• to estimate, if necessary, in terms of avoided costs, the reduction of serious adverse events frequency.
• to identify, using a qualitative approach:

• The determinants of programme acceptability and efficiency
• The appropriation by professionals of the mobilization and support program
• The impact of the program on professional practices: changes in practices and perceived effectiveness
• The conditions for programme transferability with a view to producing an Operational Model for the Implementation of Appropriateness at a Healthcare Institution Study design The project is based on a mixed method approach. Study design for the quantitative part is a Stepped-Wedge cluster randomized controlled trial, completed by a control group not receiving the intervention. The clusters are the clinical services of the Bordeaux University Hospital. Up to six volunteer clinical services will be randomly selected to determine the order in which they will start the implementation of the intervention. A control group will be made up of clinical services that meet the inclusion criteria and do not belong to the group of six participating services. The control group will receive the usual support for improving the appropriateness of care.

Qualitative section of the project will analyse the mechanisms of program effectiveness using an exploratory approach based on semi-structured interviews and direct observations of PAG.

Global proportion of patient stays appropriate regarding health cares concerned with feedback indicators available at the start of the trial.

Conditions

Any Conditions

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: RETROSPECTIVE

Study Groups

Intervention group

Services of the non-transversal clinical departments of the Bordeaux University Hospital willing to participate to the programme.

Intervention

Intervention Type: OTHER

The program intervention has three focuses : the prioritization of appropriateness indicators, the automation and visualization of the prioritized indicators, and support for practice analysis groups (PAG) based on e-feedback from automated indicators

Control group

Services of the non-transversal clinical departments of the Bordeaux University Hospital not willing to participate to the programme.

No interventions assigned to this group

Interventions

Intervention

The program intervention has three focuses : the prioritization of appropriateness indicators, the automation and visualization of the prioritized indicators, and support for practice analysis groups (PAG) based on e-feedback from automated indicators

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Services: services of the non-transversal clinical departments of the Bordeaux University Hospital.
• Health professionals: Medical and paramedical professionals working during the day or night in the participating services for at least one month and at least one day per week.
• Patients: Stays of patients hospitalized at the Bordeaux University Hospital benefiting from care targeted by the automated indicators and made available by the feedback system at the start of the trial.

Exclusion Criteria

• Services of the transversal and medico-technical departments (Medical Imaging department, Biology and Pathology department, Health Products department, Public Health department and Anesthesia-Intensive care department) and department with specific activity.
• Professionals: planning to be absent during the data collection period.
• Patients: none

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Bordeaux

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU de Bordeaux

Bordeaux, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Florence SAILLOUR-GLENISSON, Dr

Role: CONTACT

florence.saillour@chu-bordeaux.fr

05 57 57 46 40

Facility Contacts

Florence SAILLOUR, Dr

Role: primary

florence.saillour@chu-bordeaux.fr

05 57 57 46 40

Other Identifiers

CHUBX 2019/65

Identifier Type: -

Identifier Source: org_study_id