AnthropologyNCT07204626
Medical Anthropology and Migrants in Precarious Situations, Cared for in Intensive and Post-intensive Care Units
An observational study of Anthropology and Immigrant, run by Centre Hospitalier de Saint-Denis at 1 site in France.
Trial summary
Analyze the experience (perception, interpretation and incorporation - embodiment) that migrant people with low socio-economic status/precarity have of their own health conditions for which they have come to be hospitalized in the Intensive Care Unit (ICU) and Post-Resuscitation Rehabilitation Care (PRRC). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Anthropology, Immigrant, Intensive Care (ICU)
- How many people
- 100 participants
- Where
- 1 siteFrance
- Study dates
- 15 Oct 2025to 15 Jul 2026
- How long will I take part?
- 8 Months
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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
- Adult, Older adult
Study population: The study population will consist of adult migrant patients (≥18 years old) hospitalized in intensive care units (ICU) and receiving post-ICU rehabilitation care (SRPR) in selected French hospitals (Saint-Denis, Gonesse, Avicenne, Bichat). Eligible patients include those born outside France, regardless of their date of arrival, length of residence, or nationality, and who are able to communicate in French, Spanish, or Italian, either directly or via professional interpretation or cultural mediation. Participants must have a psychological and neurological state compatible with providing informed consent and participating in interviews.
Who may be able to join
- For patients:
- Male and female migrants (born outside of France and its territories, regardless of date of arrival, length of residence, or acquired nationality)
- Aged 18 years or older
- Living in or transiting through France
- With or without residence permits or legal documentation
- Hospitalized in ICUs and receiving care in post-ICU rehabilitation units (SRPR)
Show all 13Show fewer
- Providing consent to participate in the study
- Having good proficiency in French, Spanish, or Italian, or, if not, benefiting from professional interpretation (ISM) or cultural mediation ensuring effective communication
- Having a psychological and neurological state compatible with providing informed consent and taking part in an interview
- For healthcare professionals and associative actors:
- Being a healthcare, social work, or associative professional
- Involved in the medical, psycho-social, and/or legal support and care of migrant patients admitted to ICUs and SRPR
- Providing consent to participate in the study
Who cannot join
- For patients:
- Being born in France
- Being a minor (<18 years old)
- Being under guardianship or curatorship
- Having a neurological state incompatible with providing informed consent and taking part in an interview
- For healthcare professionals and associative actors:
- Not being involved in the care of migrant patients admitted to ICUs and SRPR
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site
Centre Hospitalier de Saint-Denis
Saint-Denis, France
Nolan HASSOLD, 0142356208, coordination.rechercheclinique@ghtpdfr.fr
About this study
Analyze the experience (perception, interpretation and incorporation - embodiment) that migrant people with low socio-economic status/precarity have of their own health conditions for which they have come to be hospitalized in the Intensive Care Unit (ICU) and Post-Resuscitation Rehabilitation Care (PRRC).
- Conditions
- Anthropology, Immigrant, Intensive Care (ICU), Precariousness
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| patient | Not described | |
| medical staff | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Exploration of the lived experience and perceptions of health and critical care among socio-economically vulnerable migrant patients hospitalized in intensive care units (ICU) and post-ICU rehabilitation units (SRPR), assessed through semi-structured int
Measured: 2 hours
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Oct 2025
- Study start15 Oct 2025 (estimated)
- Primary completion15 Jul 2026 (estimated)
- Study completion15 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AnthropologyStudies of the same condition, open and under way.
- 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
- 100 participants (estimated)
- Target duration
- 8 Months
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier de Saint-Denis
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07204626
- Sponsor's protocol ID
- 0110_REANIMATION
- Status last verified
- May 2025
- First submitted
- 24 Sep 2025
- Last updated
- 2 Oct 2025
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Medical Anthropology and Migrants in Precarious Situations, Cared for in Intensive and Post-intensive Care Units
- ClinicalTrials.gov ID
- NCT07204626
- Acronym / sponsor ID
- 0110_REANIMATION
- Conditions
- Anthropology, Immigrant, Intensive Care (ICU), Precariousness
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Centre Hospitalier de Saint-DenisUniversity, hospital or other
- Study start
- 15 Oct 2025 (estimated)
- Primary completion
- 15 Jul 2026 (estimated)
- Study completion
- 15 Jul 2026 (estimated)
- First posted
- 2 Oct 2025 (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.
Analyze the experience (perception, interpretation and incorporation - embodiment) that migrant people with low socio-economic status/precarity have of their own health conditions for which they have come to be hospitalized in the Intensive Care Unit (ICU) and Post-Resuscitation Rehabilitation Care (PRRC).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 8 Months
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| patient | – | – |
| medical staff | – | – |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- The study population will consist of adult migrant patients (≥18 years old) hospitalized in intensive care units (ICU) and receiving post-ICU rehabilitation care (SRPR) in selected French hospitals (Saint-Denis, Gonesse, Avicenne, Bichat). Eligible patients include those born outside France, regardless of their date of arrival, length of residence, or nationality, and who are able to communicate in French, Spanish, or Italian, either directly or via professional interpretation or cultural mediation. Participants must have a psychological and neurological state compatible with providing informed consent and participating in interviews.
Key inclusion criteria (13 listed)
- Male and female migrants (born outside of France and its territories, regardless of date of arrival, length of residence, or acquired nationality)
- Aged 18 years or older
- Living in or transiting through France
- With or without residence permits or legal documentation
- Hospitalized in ICUs and receiving care in post-ICU rehabilitation units (SRPR)
Key exclusion criteria (7 listed)
- Being born in France
- Being a minor (<18 years old)
- Being under guardianship or curatorship
- Having a neurological state incompatible with providing informed consent and taking part in an interview
- Not being involved in the care of migrant patients admitted to ICUs and SRPR
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Exploration of the lived experience and perceptions of health and critical care among socio-economically vulnerable migrant patients hospitalized in intensive care units (ICU) and post-ICU rehabilitation units (SRPR), assessed through semi-structured int
Time frame: 2 hours
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Oct 2025.
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.
Centre Hospitalier de Saint-Denis
Saint-Denis, France
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 Anthropology and Immigrant, run by Centre Hospitalier de Saint-Denis 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 13 inclusion and 7 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: opening soon, as of the sponsor's last update on 2 Oct 2025. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Exploration of the lived experience and perceptions of health and critical care among socio-economically vulnerable migrant patients hospitalized in intensive care units (ICU) and post-ICU rehabilitation units (SRPR), assessed through semi-structured int (time frame: 2 hours). 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 2 Oct 2025.