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Study on teen body drawings withdrawn before starting

NCT ID NCT07407764

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study was designed to explore how adolescents with and without borderline personality disorder represent their inner body through drawings, interviews, and questionnaires. It aimed to identify differences in the types and number of organs drawn, as well as emotional or symbolic elements. However, the study was withdrawn before enrolling any participants, so no findings are available.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Expected to start

Feb 2025

An estimate. Start dates often move.

Expected to finish

Aug 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

15 to 19 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Non-clinical cohort : 1. Adolescents aged 15 to 19 2. High school students (seconde to terminale) 3. Having signed a consent form to participate in the research, as well as their legal representative 4. Affiliated to a social security regime * Clinical cohort : 1. Adolescents aged 15 to 19 2. With a high school level (3rd year completed, transition to second year pronounced), whether enrolled or not. 3. Having signed a consent form to participate in the research and their legal representative. 4. Currently under psychiatric or pediatric care for psychiatric reasons. 5. Diagnosed or suspected of having a borderline personality disorder, 6. Affiliated to a social security regime Exclusion Criteria: Non-clinical cohort 1. Serious somatic pathology under treatment (e.g. cancer; recent or planned operations...) 2. Recognized sensory or neurological disability. 3. Known, diagnosed psychiatric pathologies (TCA, schizophrenia, etc.). 4. Refusal to participate by adolescent or parental guardians. Clinical cohort : 1. Serious somatic pathology under treatment (e.g. cancer, recent or planned operations, etc.) 2. Recognized sensory or neurological disability. 3. Refusal to participate by adolescent or parental guardians. 4. Psychomotor assessment or follow-up by the researcher.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

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