Patients Covered by AME or CSSEXPER-MSPNCT07632807
Experience and Acceptance of a New Organisational Model in Primary Care: Participatory Multi-professional Health Centres
An observational study of Patients Covered by AME or CSS, run by Assistance Publique Hopitaux De Marseille at 1 site in France.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Patients Covered by AME or CSS
- What is being tested?
- patients
- How many people
- 48 participants
- Where
- 1 siteFrance
- Study dates
- 19 Dec 2023to 25 Apr 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients covered by the Complémentaire santé solidaire (CSS) or the Aide médicale d'État (AME)
Who may be able to join
- 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;
Who cannot join
- Presenting with cognitive impairments that limit comprehension;
- Refusal to participate in the study;
Trial locations and contacts
1 site in 1 country.
About this study
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.
- Conditions
- Patients Covered by AME or CSS
- Being tested
- patients
- Medical subject headings
- Coffin-Siris syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
patientsOther
individual and group interviews
| Study group | Role | What they receive |
|---|---|---|
| Patients covered by AME or CSS who are regularly treated within a participatory coordinated care net | Not described Receives: Other: patients |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patients' experiences and care pathways
Qualitative analysis based on patients' self-reported experiences.
Measured: 1 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jun 2026
- Study start19 Dec 2023
- Primary completion25 Apr 2025
- Study completion25 Apr 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patients Covered by AME or CSSStudies of the same condition, open and under way.
- More trials run by Assistance Publique Hopitaux De MarseilleThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 48 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique Hopitaux De Marseille
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07632807
- Sponsor's protocol ID
- 2023-A00573-42
- Acronym
- EXPER-MSP
- Status last verified
- Jun 2026
- First submitted
- 26 May 2026
- Last updated
- 8 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: not decided yet
Study at a glance
From the registry record, last updated by the sponsor on 8 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Experience and Acceptance of a New Organisational Model in Primary Care: Participatory Multi-professional Health Centres
- ClinicalTrials.gov ID
- NCT07632807
- Acronym / sponsor ID
- EXPER-MSP / 2023-A00573-42
- Conditions
- Patients Covered by AME or CSS
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 48 participants (actual)
- Lead sponsor
- Assistance Publique Hopitaux De MarseilleUniversity, hospital or other
- Study start
- 19 Dec 2023 (actual)
- Primary completion
- 25 Apr 2025 (actual)
- Study completion
- 25 Apr 2025 (actual)
- First posted
- 8 Jun 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients covered by AME or CSS who are regularly treated within a participatory coordinated care net | – | Other: patients |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients covered by the Complémentaire santé solidaire (CSS) or the Aide médicale d'État (AME)
Key inclusion criteria (3 listed)
- 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;
Key exclusion criteria (2 listed)
- Presenting with cognitive impairments that limit comprehension;
- Refusal to participate in the study;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| patientsindividual and group interviews | Other | Patients covered by AME or CSS who are regularly treated within a participatory coordinated care net |
Primary outcome
Patients' experiences and care pathways
Time frame: 1 month
Qualitative analysis based on patients' self-reported experiences.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Jun 2026.
- Individual participant dataSharing planned: Undecided. not decided yet
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Patients Covered by AME or CSS, run by Assistance Publique Hopitaux De Marseille at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 8 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patients' experiences and care pathways (time frame: 1 month). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jun 2026.