Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06248268

Neuropsychological Patterns of Suicide Ideators and Suicide Attempters

Led by University of Bern · Updated on 2026-01-16

180

Participants Needed

1

Research Sites

125 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present study consists of 3 projects in total and aims to investigate the (neuro-) psychological patterns from suicidal ideation to suicidal behavior as well as the effects and feasibility of ASSIP Home Treatment. The overall aim of project 1 is to determine (neuro-) psychological differences between suicide attempters, suicide ideators, a clinical control group, and healthy controls. Study participants in project 1 will participate in a one-time (neuro-) psychological assessment. Project 1 of this study is an observational cross-sectional study with four groups that will be conducted at the University Hospital of Psychiatry and Psychotherapy Bern (Switzerland): Patients with at least one suicide attempt in their past (SUAT), patients with suicidal ideation (SUID), patients from the same clinical cohort, without neither suicidal behavior or ideation (CLIN) and the healthy group (HLTH). The cohorts to be examined (SUAT \& SUID) will be compared to the two control groups (CLIN \& HLTH). Only people who have signed the informed consent and meet the eligibility criteria can participate in this study.

CONDITIONS

Official Title

Neuropsychological Patterns of Suicide Ideators and Suicide Attempters

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent
  • Age 18 years or older
  • For the suicide attempt group: at least one previous suicide attempt
  • For the suicidal ideation group: current suicidal thoughts
  • For the clinical control group: current psychiatric disorder treated as inpatient, day-care, or outpatient
  • For the healthy control group: no additional inclusion criteria
Not Eligible

You will not qualify if you...

  • Serious cognitive impairment
  • Current psychotic disorder
  • Current medication that impairs attention, reaction, or cognitive functions
  • Unable to follow study procedures (e.g., insufficient German language skills, previous enrollment in this study)
  • For the suicidal ideation group: any previous suicidal behavior
  • For the clinical and healthy control groups: any previous suicidal behavior or suicidal ideation
  • For the healthy control group: current psychiatric disorder treated as inpatient, day-care, or outpatient

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital of Psychiatry and Psychotherapy, University of Bern

Bern, Switzerland, 3008

Actively Recruiting

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Research Team

A

Anja C. Gysin-Maillart, PD Dr. phil.

CONTACT

K

Kristina Adorjan, Prof. Dr. med.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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