Can 8 therapy sessions stop a second suicide attempt?
NCT ID NCT06238414
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This trial tests whether a short, 8-session psychological intervention can reduce the risk of another suicide attempt in people hospitalized after a medically serious attempt. Participants are adults over 16 who stay in the hospital for at least 24 hours. Half receive the therapy, while the other half get standard care. Researchers track repeat attempts and related outcomes for a year to see if the therapy makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- An 8-session early psychological intervention combining dialectical behavior therapy, mentalization-based therapy, and narrative approaches (adapted from ASSIP therapy)
- What this could lead to
- If effective, this brief therapy could become a standard early intervention for people hospitalized after a serious suicide attempt, potentially reducing repeat attempts and saving lives.
- What could go wrong
- The trial is small (75 participants) and early, so results may not apply broadly. The intervention's success depends on patient engagement and follow-up, and it may not prevent all repeat attempts.
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
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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
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75 people
The number who actually took part.
- Started
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Dec 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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16 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Older than 16 years. * Remaining hospitalized for 24 hours or more at HUVH and HCP after a MSSA for 24 or more (\> = 24 hours). * Needing specialized care units (including Intensive Care Units, Hyperbaric Camera Units, Burned Units, Semicritical Units) * Needing specialized surgical treatment, excluding superficial cuts * Needing extensive medical treatment and observation (gastric lavage, activated charcoal, observation of neurological tests or other complementary tests) * MSSA with high lethality methods (precipitation, hanging, firearm, stabbing) needing hospitalization for 24 or more hours, regardless of the treatment unit. Exclusion Criteria: * Patients with suicide attempts who were discharged in \<24 h * Patients under 16 years. * Patients with mild to severe cognitive impairment. * Lack of informed consent.
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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.
Contacts and locations
Locations
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Anna Beneria
Barcelona, Spain, 08035, Spain
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Other studies related to the condition(s) this trial covers.
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