Clinical trial Recruiting at 1 site Observational Ages 18 and up

Investigating psychological patterns in individuals with suicidal thoughts and behaviors

Official title: Differences Between Suicide Attempters and Suicide Ideators. Influence of the Brief Therapy ASSIP on Neuropsychological Correlates and Psychological Process Factors (NePsyASSIP HT) - Project 1

Run by University of Bern · NCT06248268 · Data updated 2026-11-12

This study is trying to understand the mental differences between people who have thought about or attempted suicide and those who haven't, to see if a new home treatment could help those at risk.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment180 (estimated)
SponsorUniversity of Bern
Academic / other
Locations1 site (Bern)
StatusRecruiting
StartedAugust 8, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedJanuary 16, 2026
Trial IDNCT06248268 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with a history of suicide attempts or current suicidal ideation.

Probably not a fit

Patients with serious cognitive impairments or psychotic disorders may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to explore the neuropsychological differences between individuals who have attempted suicide, those with suicidal ideation, a clinical control group, and healthy controls. Participants will undergo a one-time neuropsychological assessment at the University Hospital of Psychiatry and Psychotherapy Bern in Switzerland. The study seeks to identify psychological factors that differentiate these groups and to assess the feasibility of a specific home treatment approach for those at risk. The findings could enhance understanding of the transition from suicidal thoughts to actions.

Why it matters

Potential benefit: If successful, this study could lead to improved identification and treatment strategies for individuals at risk of suicide.

How similar studies have gone: While there have been studies on suicide risk factors, this specific approach focusing on neuropsychological patterns is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Subjects fulfilling the following inclusion criteria are eligible for the study:

* Informed consent as documented by signature
* Age ≥ 18 years

Additional inclusion criterion for the SUAT group in project 1:

• At least one previous suicide attempt

Additional inclusion criterion for the SUID group in project 1:

• Suicidal ideation

Additional inclusion criterion for the CLIN group in project 1:

• Current psychiatric disorder treated on an inpatient, day-care or outpatient basis For the HLTH group, no further inclusion criteria are formulated.

Exclusion Criteria:

The presence of any one of the following exclusion criteria leads to exclusion of the subject:

* Serious cognitive impairment
* Any current psychotic disorder
* Any current medication, which substantially impairs the attention span, reaction rate or any other relevant cognitive functions
* Inability to follow the procedures of the study (e.g., insufficient mastery of the German language, previous enrolment into the current study)

Additional exclusion criterion for the SUID group:

• Previous suicidal behavior

Additional exclusion criteria for the CLIN and HLTH groups:

* Previous suicidal behavior
* Suicidal ideation

Additional exclusion criterion for the HLTH group:

• Current psychiatric disorder treated on an inpatient, day-care or outpatient basis

Where it's running

  • University Hospital of Psychiatry and Psychotherapy, University of Bern
    Bern, Switzerland
    Recruiting

Study contacts

  • Principal investigator: Anja C. Gysin-Maillart, PD Dr. phil. — University of Bern, University Hospital of Psychiatry, Translational Research Center
  • Study coordinator: Anja C. Gysin-Maillart, PD Dr. phil.
  • Email: anja.gysin-maillart@unibe.ch
  • Phone: +41 (0) 31 632 88 11

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.