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RecruitingNCT04953273

Effectiveness of case Management Algorithm on Clinical Outcome After Consultations Requested in PTSD; Violence-Related Symptom

The registry lists this study as recruiting. Study locations are listed in France. Confirm recruitment at each site. It is testing case Management Algorithm on Clinical Outcome After Consultations Requested for PTSD; Violence-Related Symptom.

PTSD, Violence-Related SymptomOtherOver 18 Years
In plain English

Key information made simple

What is this study testing?

This study is testing whether Vigitrauma may be useful for adults experiencing ptsd.

What would participation involve?

Participants may complete study activities around Vigitrauma, 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: July 6, 2021
Recruitment status
Recruiting
Enrollment listed in the registry
756
Sponsor
University Hospital, Lille
Sponsor type
Hospital / academic medical center
Study type
Other
Intervention type
OTHER
Study phase
Not clearly listed
Locations
France
Age range
Over 18 Years
Official registry ID
NCT04953273
Official title
Effectiveness of a Case Management Algorithm on Clinical Outcome After Consultations Requested in a Clinical Forensic Medicine Unit by Female Victims of Violence

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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 · 8 sites
  • University Hospital, Amiens
    Amiens
    Site status: Not Yet Recruiting
  • General Hospital, Boulogne sur Mer
    Boulogne-sur-Mer
    Site status: Not Yet Recruiting
  • University Hospital, Caen
    Caen
    Site status: Not Yet Recruiting
  • General Hospital, Creil
    Creil
    Site status: Not Yet Recruiting
  • University Hospital, Lille
    Lille
    Site status: Recruiting
  • University Hospital, Rouen
    Rouen
    Site status: Not Yet Recruiting
  • General Hospital, Saint-Quentin
    Saint-Quentin
    Site status: Not Yet Recruiting
  • General Hospital, Valenciennes
    Valenciennes
    Site status: Not Yet Recruiting
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: A considerable body of research has demonstrated that women who are victims of interpersonal violence are at substantially elevated risk for the development of post-traumatic stress disorder (PTSD). In France, victims can request a medico-legal examination in a clinical. The study team can confirm the exact objective and what it means for you.

Why is the study type not clearly categorized?

The study type is not clearly categorized in the public registry. Focus on the objective, required tasks, visits, any intervention, and eligibility criteria, then ask the study team to confirm.

Who might this study be for?

This study may concern people with ptsd; age range: Over 18 Years. The criteria appear fairly broad, 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?

The public registry does not clearly describe all participation steps. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.

What risks or points should I check?

The public registry does not make the main risk category clear. Ask the study team what activities are required, what could feel uncomfortable, how safety is monitored, and what happens if you want to stop. 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 University Hospital, Lille, 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 recruiting. Individual sites may have different statuses. The research team must confirm whether a site is open and whether you meet the criteria.

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