Classification of Patient Therapeutic Education Programs Components : Etude CONCErTo

Chronic Disease Clinical Trial

— CONCErTo  

Official title:

Development of a Classification of the Components of Patient Therapeutic Education Interventions That Can Impact Their Results and Can Ensure Their Continued Existence CONCErTo Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02717182
• Other study ID #: PREPS1439089
• Status: Recruiting
• Start date: April 2016
• Est. completion date: December 2019

Study information

• Verified date: May 2019
• Source: Central Hospital, Nancy, France
• Contact: Anne-Christine Rat, MD, PhD
• Phone: +33383153196
• Email: ac.rat[@]chu-nancy.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Interest in patient therapeutic education (PTE) is increasing: in France PTE was included within the 2009 "Hospital, Patient, Health and Territory" law as an essential component of the patient healthcare pathway.

PTE is a complex intervention: its delivery is variable and may vary according to its content, functioning, providers, targeted patients, environment and even its objectives. These differences impact the expected results and make difficult the evaluation of PTE interventions. To overcome this difficulty, it is essential to describe precisely the intervention, the processes and the implementation of PTE that are usually not known. PTE interventions need today a global understanding of their mechanisms constituting their complexity.

CONCErTo study aims at developing a classification of the different elements composing a PTE intervention that can impact their results and can ensure their continued existence.

Mechanisms implemented during PTE interventions will be analyzed by a qualitative research. The investigators wish to identify organizational, pedagogical, psychosocial, medical or contextual elements that can impact the results, the patients' participation and the continuity of the program.

The perspective of this research is to improve the understanding of PTE by providing thorough description of the interventions. This work will help stakeholders to better interpret the results of their interventions, to improve the transferability, the implementation and finally to determine which are the elements able to improve patients' health status.

Description:

This research is an observational study with no intervention. It uses qualitative methods.

The development of the classification consists in 3 phases: a preliminary phase of literature review, an investigation phase and a phase of elaboration of the classification.

Preliminary phase To deepen the questioning of the research, a literature review will be realized on concepts and models as well as on tools and methods used in the published PTE interventions.

Investigation phase

This step uses qualitative methods with 3 types of data collection:

• Semi structured interviews: individual interview will be realized with health care professionals and Therapeutic Patient Education stakeholders (trainers, professional network, decisions makers..). Focus groups will be organized with patients after completion of a therapeutic patient education program.

• In situ observations of the sessions

• Analysis of the documents surrounding the implementation of the interventions: reports, grey literature, applications; the objective is to capture the environment supervising the programs

The investigators plan to include up to 15 programs. However, this number will be adjusted according to the principle of data saturation.

Programs will be selected to ensure variability: the investigators will include hospital based or community based programs, programs led by general practitioners or specialists, with or without patients' implication, recent or experimented programs.

For each program, at least 3 health care professionals and one focus group with patients will be conducted. It will be completed by observation of education sessions.

Other actors (patients' proxies, associations playing a role in the conception or animation of the programs, designers, coordinators, general practitioners, experts of French territorial organization, trainers..;) will complete the data.

The aim of this step is not only to describe the practices but also to interview the experts on the elements they think can impact the results of PTE interventions.

Phase of elaboration of the classification Thematic and content data analyses are scheduled. Concept mapping method will be used to develop the classification.

The classification will be reviewed by experts having not participated to the previous steps.

Validation of the classification :

Applicability and relevance of the classification will be tested with 15 programs in various medical domains.

The classification will then be used in a cohort of patients before and after PTE intervention.

With this classification (or list), recommendations to describe PTE programs will be published.

Eventually, the aim of the recommendations, is to improve the understanding of PTE by providing thorough description of the interventions. This work will help stakeholders to better interpret the results of their interventions, to improve the transferability, the implementation and finally to determine which are the elements able to improve patients' health status.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: December 2019
• Est. primary completion date: December 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• patients following a patient education program

• professionals involved in a patients education program

Exclusion Criteria:

-

Related Conditions & MeSH terms

• Chronic Disease

Intervention

Other:
• interviews
interviews

Locations

Country	Name	City	State
France	Rat Anne-Christine	Nancy

Sponsors (2)

Lead Sponsor	Collaborator
Central Hospital, Nancy, France	Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient-reported elements of patient therapeutic education	Focus groups of patients	2 years
Primary	Heath care professionals-reported elements of patient therapeutic education	Individual Interviews of health care professionals	2 years