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Not Yet RecruitingNCT07207018

Effectiveness of CFTSI (Child and Family Traumatic Stress Intervention) in PTSD

This study is not yet recruiting in France. It is testing CFTSI (Child and Family Traumatic Stress Intervention) for PTSD.

PTSD, PTSD (PTSD)BehavioralFrom 7 Years to 17 Years

The public registry lists this study as not yet recruiting. Check the official record and ask the research team when recruitment may open.

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France · 1 site
  • CHU Montpellier
    Montpellier, Herault
    Site status: Not listed — confirm with the team
In plain English

Key information made simple

What is this study testing?

This study is testing whether CFTSI (Child and Family Traumatic Stress Intervention) may be useful for adolescents experiencing ptsd.

What would participation involve?

Participants may take part in CFTSI (Child and Family Traumatic Stress Intervention), attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in France.

Who is it mainly for?

This study appears to be mainly for adolescents with ptsd. Because it involves minors, a parent or guardian may need to be involved.

What should you check before joining?

Ask about how many sessions are required and who delivers them, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, what role parents or guardians have in the process.

What to expect

Your next step

Study sites are listed in the registry. Recruitment status can differ between sites. Ask the research team to confirm the location, any in-person visits, time commitment, costs or compensation, and participation criteria.

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateEstimated: December 2025
Recruitment status
Not Yet Recruiting
Enrollment listed in the registry
140
Sponsor
University Hospital, Montpellier
Sponsor type
Hospital / academic medical center
Study type
Behavioral
Intervention type
Psychotherapy / behavioral intervention
Study phase
Not clearly listed
Locations
France
Age range
From 7 Years to 17 Years
Official registry ID
NCT07207018
Official title
Early Intervention After Traumatic Exposure in Children and Adolescents: a Randomized Controlled Trial of the Effectiveness of Child and Family Traumatic Stress Intervention (CFTSI).
Official source
Official registry link

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Study ID: NCT07207018. We help you review the study, but cannot decide medical eligibility.
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 this interventional research is to evaluate the effectiveness of CFTSI in reducing post-traumatic symptoms measured using the CPC, child version, at the end of CFTSI treatment in children and adolescents aged between 7 and 17 years, exposed to an ET in the last 3. 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 CFTSI (Child and Family Traumatic Stress Intervention), non-specific psychological support therapy. 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: From 7 Years to 17 Years. The criteria appear strict, 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 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 University Hospital, Montpellier, 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 yet recruiting. Check the official record and ask the research team when recruitment may open.

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