How medicalized residential care influences care plans for vulnerable palliative patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will include adults (≥18) receiving palliative care who live in one of two medicalized residential care (LAM) regions of Alsace, France. Researchers will collect clinical and contextual information from medical records and care teams to identify factors that influence the development of care plans. The study focuses on vulnerable patients in palliative settings and excludes those who refuse participation. The goal is to describe patterns and drivers of care planning in LAM settings rather than to test a specific treatment.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult subject (≥18 years old)
* Subject residing in one of the two LAM regions of Alsace (France) at the time of the study and suffering from a palliative-care condition (the nature of the condition (or conditions) is not specified)

Exclusion Criteria:

\- Refusal to participate in the study

Where it's running

• Service d'Accompagnement et de Soins Palliatifs - CHU de Strasbourg - France
  Strasbourg, France Recruiting

Study contacts

• Study coordinator: Johanna LAPLACE, MD
• Email: johanna.laplace@chru-strasbourg.fr
• Phone: 33 3 88 11 65 80

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.