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Not yet recruiting NCT07204626

Medical Anthropology and Migrants in Precarious Situations, Cared for in Intensive and Post-intensive Care Units

Observational Anthropology Immigrant Intensive Care (ICU) Precariousness

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Anthropology, Immigrant, Intensive Care (ICU), Precariousness. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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).

Primary outcome measures

  • 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]

Eligibility criteria

Inclusion criteria

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)

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

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Centre Hospitalier de Saint-Denis — Saint-Denis

Identifiers

NCT: NCT07204626 · 0110_REANIMATION

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗