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UnknownNCT03991611

Administration of the IPREA3 questionnaire for PTSD

This study has an unknown status in France. It is testing Administration of the IPREA3 questionnaire for PTSD.

PTSD, Critical IllnessBehavioralOver 18 Years

Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.

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.

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: 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

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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.

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 · 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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