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Can a website help suicidal teens? new study tests digital support

NCT ID NCT05900700

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 This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a website called eYST, designed to provide social support for teenagers at risk for suicide. Researchers wanted to see if the website was easy to use and helpful for 75 teens and their chosen support adults. The study focused on gathering feedback and measuring how often people used the site.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
eYST website (a psychoeducational social support program)
What this could lead to
If this approach proves helpful, it could offer a new way to support suicidal teens by connecting them with trusted adults through a website.
What could go wrong
This was a small, early-stage study focused on usability, not on whether the intervention actually reduces suicide risk. The results may not apply to all teens.

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.

Participants

75 people

The number who actually took part.

Started

Nov 2023

Finished

Sep 2024

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

13 to 17 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: 1. Inpatient psychiatric patients who have attempted suicide or have documented Suicide ideation (SI) and a plan to harm themselves at admission. 2. Understand written and spoken English. 3. Own a smartphone or mobile phone. 4. Willing and able to complete enrollment procedures. 5. Parent or guardian and youth able to understand the nature of the study and provide written informed consent and assent for youth 6. Patients who are able to provide at least one verifiable contact for emergency or tracking purposes. Exclusion Criteria: 1. Patients with active psychosis. 2. Patients experiencing substance withdrawal. 3. Currently enrolled in other treatment studies for the symptoms and behaviors targeted. 4. Patient unwilling or unable to wear a mask during in person study procedures, if mandated due to current COVID/health safety guidelines. 5. Patients who in the judgment of the investigator would have an unfavorable risk or benefit profile with respect to eYST. 6. Any other psychiatric or medical condition or custody arrangement that in the investigators' opinion would preclude informed consent or assent or participation in the trial.

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Conditions

The condition(s) this trial relates to.

Suicide

As listed by the trial registrant

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

Contacts and locations

Locations

  • Michigan Medicine

    Ann Arbor, Michigan, 48109, United States

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Other studies related to the condition(s) this trial covers.