Experience and Acceptance of a New Organisational Model i... | NCT07632807

Studies
Experience and Acceptance of a New Organisational Model in Primary Care: Participatory Multi-professional Health Centres

NCT07632807

Sponsor

Assistance Publique Hopitaux De Marseille

Status

Completed

Last Update Posted

Jun 8, 2026Actual

Enrollment

48Actual

Phase

Not provided

Conditions

Patients Covered by AME or CSS

Interventions

patients

Countries

France

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Jun 2026

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Dec 19, 2023Actual

Primary Completion Date

Apr 25, 2025Actual

Completion Date

Apr 25, 2025Actual

First Submitted Date

May 26, 2026

First Submission Date that Met QC Criteria

Jun 2, 2026

First Posted Date

Jun 8, 2026Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jun 2, 2026

Last Update Posted Date

Jun 8, 2026Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

A qualitative study employing a grounded theory approach, using semi-structured interviews and focus group discussions with patients participating in the participatory scheme under investigation, as well as professionals who took part in the scheme or partners, recruited through theoretical sampling. Inductive analysis following full transcription of the interviews. Triangulation of the analysis by at least two researchers.

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

48Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Patients covered by AME or CSS who are regularly treated within a participatory coordinated care net			Other: patients

Interventions

Name	Type	Description	Arm Group Labels	Other Names
patients	Other	individual and group interviews	Patients covered by AME or CSS who are regularly treated within a participatory coordinated care net

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Patients' experiences and care pathways	Qualitative analysis based on patients' self-reported experiences.	1 month

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion criteria:

Patients aged 18 years and over;
Patients covered by the Complémentaire santé solidaire (CSS) or the Aide médicale d'État (AME)
Whose general practitioner (or designated referring doctor for patients covered by the AME) is one of the general practitioners at the Peyssonnel health centre;

Exclusion criteria:

Presenting with cognitive impairments that limit comprehension;
Refusal to participate in the study;

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

Not provided

Standard Ages

AdultOlder Adult

Study Population

Patients covered by the Complémentaire santé solidaire (CSS) or the Aide médicale d'État (AME)

Sampling Method

Non-Probability Sample

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Not provided

Locations

Facility	Status	City	State	ZIP	Country	Contacts
MSP Universitaire Peyssonnel		Marseille		13003	France

IPD Sharing Statement Module

Plan to Share IPD

Undecided

Description

not decided yet

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided

Condition Browse Module

MeSH Terms

ID	Term
C536436	Coffin-Siris syndrome

Ancestor Terms

Not provided

Browse Leaves

Not provided

Browse Branches

Not provided