Then choose your country and confirm availability with each study site.
In plain English
Key information made simple
What is this study testing?
This study is testing whether surveys or interviews may be useful for adults experiencing ptsd.
What would participation involve?
Participants may answer questionnaires, join interviews, or provide follow-up information, 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.
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
What are the exact eligibility criteria, and what could exclude someone?
How many visits, assessments, or follow-ups are expected, and over what period?
What risks, side effects, practical burdens, or alternatives should be understood first?
Who should be contacted to confirm locations, timing, compensation, and next steps?
Study clarity
Things to check before joining
Study start dateStarted: November 1, 2019
Recruitment status
Unknown
Enrollment listed in the registry
3,312
Sponsor
Centre Hospitalier of Chartres
Sponsor type
Unknown or unclear
Study type
Behavioral
Intervention type
OTHER
Study phase
Not clearly listed
Locations
France
Age range
Over 18 Years
Official registry ID
NCT03991611
Official title
Tailored Multicomponent Program for Discomfort Reduction in Critically il Patients May Decrease Post-traumatic Stress Disorder in General ICU Survivors at One Year
Ask HopeStage to help me review this study
This record does not confirm open recruitment. We can help you understand it and explore other studies.
Study ID: NCT03991611. 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.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
France · 33 sites
CHU Angers
Angers
Site status: Not listed — confirm with the team
CHU d'Angers
Angers
Site status: Not listed — confirm with the team
CH d'Auxerre
Auxerre
Site status: Not listed — confirm with the team
CH de Blois
Blois
Site status: Not listed — confirm with the team
Clinique Convert
Bourg-en-Bresse
Site status: Not listed — confirm with the team
CH Bourges
Bourges
Site status: Not listed — confirm with the team
Hôpital Louis Pasteur
Chartres
Site status: Not listed — confirm with the team
CHU de Dijon
Dijon
Site status: Not listed — confirm with the team
CH de Douai
Douai
Site status: Not listed — confirm with the team
CH Emile Roux
Le Puy-en-Velay
Site status: Not listed — confirm with the team
CH de Lens
Lens
Site status: Not listed — confirm with the team
Hôpital Edouard Herriot
Lyon
Site status: Not listed — confirm with the team
Hôpital Européen de Marseille
Marseille
Site status: Not listed — confirm with the team
Hôpital Nord_APHM
Marseille
Site status: Not listed — confirm with the team
Hôpital Nord_APHM
Marseille
Site status: Not listed — confirm with the team
CH de Mâcon
Mâcon
Site status: Not listed — confirm with the team
CH de l'Agglomération Montargoise
Montargis
Site status: Not listed — confirm with the team
GHR Mulhouse Sud-Alsace
Mulhouse
Site status: Not listed — confirm with the team
Clinique Ambroise Paré
Neuilly-sur-Seine
Site status: Not listed — confirm with the team
Hôpital Pasteur 2_CHU de Nice
Nice
Site status: Not listed — confirm with the team
Hôpital Saint-Louis_APHP
Paris
Site status: Not listed — confirm with the team
Gaston Cordier_GH La Pitié-Salpêtrière-Charles Foix_APHP
Paris
Site status: Not listed — confirm with the team
GH La Pitié-Salpêtrière-Charles Foix_APHP
Paris
Site status: Not listed — confirm with the team
Husson Mourier_GH La Pitié-Salpêtrière-Charles Foix_APHP
Paris
Site status: Not listed — confirm with the team
CHU de Poitiers
Poitiers
Site status: Not listed — confirm with the team
Hôpital privé Claude Galien
Quincy-sous-Sénart
Site status: Not listed — confirm with the team
CH Victor Provo
Roubaix
Site status: Not listed — confirm with the team
NCT+ - St Gatien
Saint-Cyr-sur-Loire
Site status: Not listed — confirm with the team
Nouvel Hôpital Civil_CHU de Strasbourg
Strasbourg
Site status: Not listed — confirm with the team
Hôpital de Hautepierre_CHU de Strasbourg
Strasbourg
Site status: Not listed — confirm with the team
Hôpital Sainte Musse
Toulon
Site status: Not listed — confirm with the team
CHRU de Tours
Tours
Site status: Not listed — confirm with the team
CH de Troyes
Troyes
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: Reducing discomfort in the intensive care unit (ICU) should be beneficial to longterm outcomes. This study assesses whether a tailored multicomponent program for discomfort reduction may be effective in reducing post-traumatic stress disorder (PTSD) symptoms at 1-year in. The study team can confirm the exact objective and what it means for you.
What is a behavioral study?
This appears to be a behavioral / psychological / psychosocial study involving Administration of the IPREA3 questionnaire, Immediate feedback through electronic reminder messages, Targeted interventions in each ICU to reduce discomforts, 6 months follow-up to assess the prevalence of PTSD symptoms, 1 year follow-up to assess psychiatric morbidity. 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.
What would I likely need to do?
You may take part in sessions or exercises related to habits, thoughts, emotions, or behaviors. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
Could this study affect my mood, habits, motivation, or stress?
Behavioral studies can involve habits, emotions, motivation, stress, sleep, or ways of thinking. Ask whether the intervention could affect your mood or stress, and who to contact if you feel worse. 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 Centre Hospitalier of Chartres, which appears to be unknown or unclear. 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?
Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.
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