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CompletedNCT05461521

PTSD in Relatives of Patients Admitted to the ICU: a Observational, Prospective Study (FAME Observational)

This study is completed in France. It is testing Family members of patients admitted to the ICU for PTSD.

PTSD, Family MembersObservationalOver 18 Years

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

Then choose your country and confirm availability with each study site.

In plain English

Key information made simple

What is this study testing?

This observational study follows adults living with ptsd to understand their experience, outcomes, or changes over time.

What would participation involve?

Participants may complete study activities around Family members of patients admitted to the ICU, attend study visits with the research team. The registry lists locations in France.

Who is it mainly for?

This study appears to be mainly for adults with ptsd.

What should you check before joining?

Ask about whether there is a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateStarted: December 15, 2022
Recruitment status
Completed
Enrollment listed in the registry
1,346
Sponsor
Nantes University Hospital
Sponsor type
Hospital / academic medical center
Study type
Observational
Intervention type
OTHER
Study phase
Not clearly listed
Locations
France
Age range
Over 18 Years
Official registry ID
NCT05461521
Official title
Post-traumatic Stress Disorder in Relatives of Patients Admitted to the ICU: a Multicenter, Observational, Prospective Study (FAME Observational)

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Study ID: NCT05461521. We help you review the study, but cannot decide medical eligibility.

Check recruitment and locations

Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

France · 55 sites
  • CH Angoulême
    Angoulême, France
    Site status: Not listed — confirm with the team
  • Hôpital Privé d'Antony
    Antony, France
    Site status: Not listed — confirm with the team
  • CH d'Argenteuil
    Argenteuil, France
    Site status: Not listed — confirm with the team
  • CH de Bastia
    Bastia, France
    Site status: Not listed — confirm with the team
  • CH Beauvais
    Beauvais, France
    Site status: Not listed — confirm with the team
  • Hôpital Nord Franche Comté
    Belfort, France
    Site status: Not listed — confirm with the team
  • CH de Béthune
    Beuvry, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Avicenne
    Bobigny, France
    Site status: Not listed — confirm with the team
  • CHU de Bordeaux - Hôpital Saint-André
    Bordeaux, France
    Site status: Not listed — confirm with the team
  • CHU de Bordeaux - Hôpital Pellegrin
    Bordeaux, France
    Site status: Not listed — confirm with the team
  • AP-HP Hôpital Ambroise Paré
    Boulogne, France
    Site status: Not listed — confirm with the team
  • CH de Boulogne-sur-Mer
    Boulogne-sur-Mer, France
    Site status: Not listed — confirm with the team
  • CHU de Brest
    Brest, France
    Site status: Not listed — confirm with the team
  • CH de Chartres
    Chartres, France
    Site status: Not listed — confirm with the team
  • CH de Cholet
    Cholet, France
    Site status: Not listed — confirm with the team
  • CHU Clermont-Ferrand - Centre Jean Perrin
    Clermont-Ferrand, France
    Site status: Not listed — confirm with the team
  • CHU Clermont-Ferrand - Hôpital Gabriel Montpied
    Clermont-Ferrand, France
    Site status: Not listed — confirm with the team
  • CH de Dieppe
    Dieppe, France
    Site status: Not listed — confirm with the team
  • CHU de Dijon
    Dijon, France
    Site status: Not listed — confirm with the team
  • CH de Fréjus - Saint Raphaël
    Fréjus, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Raymond Poincaré
    Garches, France
    Site status: Not listed — confirm with the team
  • CHU de Grenoble Alpes
    Grenoble, France
    Site status: Not listed — confirm with the team
  • GHEF- Site de Marne de la Vallée
    Jossigny, France
    Site status: Not listed — confirm with the team
  • CHD Vendée
    La Roche-sur-Yon, France
    Site status: Not listed — confirm with the team
  • CH de la Rochelle
    La Rochelle, France
    Site status: Not listed — confirm with the team
  • CH Versailles - Hôpital André Mignot
    Le Chesnay, France
    Site status: Not listed — confirm with the team
  • CH du Mans
    Le Mans, France
    Site status: Not listed — confirm with the team
  • CHU de Lille - Hôpital Roger Salengro
    Lille, France
    Site status: Not listed — confirm with the team
  • GHB Sud - Hôpital de Lorient
    Lorient, France
    Site status: Not listed — confirm with the team
  • CHU De Lyon - Hôpital Edouard Herriot
    Lyon, France
    Site status: Not listed — confirm with the team
  • AP-HM - Hôpital Nord
    Marseille, France
    Site status: Not listed — confirm with the team
  • Hôpital Privé Jacques Cartier
    Massy, France
    Site status: Not listed — confirm with the team
  • GHI le Raincy Montfermeil
    Montfermeil, France
    Site status: Not listed — confirm with the team
  • CHU de Montpellier - Hôpital Lapeyronie
    Montpellier, France
    Site status: Not listed — confirm with the team
  • CHU de Montpellier - Hôpital Saint-Eloi
    Montpellier, France
    Site status: Not listed — confirm with the team
  • CHU de Nantes
    Nantes, France
    Site status: Not listed — confirm with the team
  • Clinique Ambroise Paré
    Neuilly-sur-Seine, France
    Site status: Not listed — confirm with the team
  • CHR d'Orléans
    Orléans, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Saint-Louis
    Paris, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Cochin
    Paris, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital La Pitié Salpêtrière
    Paris, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Tenon
    Paris, France
    Site status: Not listed — confirm with the team
  • APHP Hôpital Saint-Antoine
    Paris, France
    Site status: Not listed — confirm with the team
  • CHI Poissy
    Poissy, France
    Site status: Not listed — confirm with the team
  • CH René Dubos
    Pontoise, France
    Site status: Not listed — confirm with the team
  • CH de Saint-Lô
    Saint-Lô, France
    Site status: Not listed — confirm with the team
  • CH de Saint-Nazaire
    Saint-Nazaire, France
    Site status: Not listed — confirm with the team
  • Hôpital du Pays Salonais
    Salon-de-Provence, France
    Site status: Not listed — confirm with the team
  • CH de Bassin de Thau
    Sète, France
    Site status: Not listed — confirm with the team
  • CH de Saint-Malo
    St-Malo, France
    Site status: Not listed — confirm with the team
  • Hôpital Foch
    Suresnes, France
    Site status: Not listed — confirm with the team
  • CH de Tourcoing - Hôpital Guy Chatiliez
    Tourcoing, France
    Site status: Not listed — confirm with the team
  • Ch Bretagne Atlantique - site de Vannes
    Vannes, France
    Site status: Not listed — confirm with the team
  • CH de Vichy
    Vichy, France
    Site status: Not listed — confirm with the team
  • Institut Gustave Roussy
    Villejuif, France
    Site status: Not listed — confirm with the team
Guadeloupe · 1 site
  • CHU La Guadeloupe
    Pointe-à-Pitre, France
    Site status: Not listed — confirm with the team
In practice

For you

Participation may contribute to research. Personal benefit is not guaranteed.

Ask the research team to explain the activities, time commitment, and follow-up involved.

Study sites are listed. Confirm the relevant site and any travel before making plans.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is this study trying to understand?

Based on the public registry summary, this study is trying to understand: The aim of the present research is to set up a large multicentric, prospective cohort of family members of patients admitted to intensive care. The data collected will concern the patients and their family members, the caregivers and the functioning of the services during the. The study team can confirm the exact objective and what it means for you.

Is this an interview, survey, or observational study?

This appears to be a interview / survey / observational study involving Family members of patients admitted to the ICU, Health care professionals, Patients. Phase is mainly useful to check for medication studies and some device studies.

Who might this study be for?

This study may concern people with ptsd; age range: Over 18 Years. The criteria appear fairly specific, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.

Does a loved one or caregiver need to be involved?

The public registry appears to mention a loved one, caregiver, or family involvement. Ask whether that person must participate, provide information, attend visits, or simply be available if needed. The study team must confirm what is required.

Could the questions feel emotionally difficult or personal?

If the study involves interviews or questionnaires, some questions may feel personal or emotionally sensitive. Ask whether you can skip questions, pause, stop, and how your answers will be protected. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.

Will I need to travel or attend in-person visits?

The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.

Who is behind this study?

This study is sponsored by Nantes University Hospital, which appears to be a hospital or academic medical center. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.

Can I still join this study?

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

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