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Can a Smartphone-Personalized therapy curb suicidal thoughts?

NCT ID NCT07749391

Symptom relief Sponsor: University of California, San Diego Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 06, 2026 · Last updated Sep 11, 2026 · Updated 6 times

Summary

This trial tests a new, brief coaching program called PRECISE for young adults aged 18-26 who experience suicidal thoughts. Participants use a smartphone app to report their emotions and thoughts several times a day, and this personal data is used to tailor coaching sessions with coping skills and safety planning. The goal is to see if this personalized approach can reduce emotional distress and suicidal thoughts, and improve emotion regulation.

What this could mean

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

Active substance
PRECISE, a brief, personalized coaching intervention delivered via videoconferencing, using participants' own smartphone survey data to tailor coping skills and safety planning.
What this could lead to
If successful, this could lead to a more personalized, effective approach to reducing suicidal thoughts in young adults, potentially saving lives by addressing individual triggers.
What could go wrong
This is a small, early-stage pilot study, so results may not apply broadly. The intervention is brief and adjunctive, and its success depends on participant engagement and the accuracy of personalized data.

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

35 people

The number who actually took part.

Started

May 2024

Finished

Sep 2026

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

18 to 26 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: * Age 18-26 years * Endorsement of active suicidal ideation on the Columbia-Suicide Severity Rating Scale (C-SSRS) (score \>2, or past-month thoughts of killing self) * English fluency * Willingness to provide contact information for a key support person to be contacted as part of the study's risk and safety plan Exclusion Criteria: * Unable to read English * Diagnosis of a psychotic or severe thought disorder (e.g., schizophrenia, bipolar disorder with psychotic features)

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Conditions

The condition(s) this trial relates to.

Behavior Emotional Regulation Suicidal Ideation

As listed by the trial registrant

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

Suicidal thoughts and behaviors

Contacts and locations

Locations

  • Stein Clinical Research Building

    La Jolla, California, 92093, United States

More trials for these conditions

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