Completed

FACEFacing Adverse Childhood Experiences Using New Technologies

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Self-Control+1

+ Emotional Regulation

+ Behavior

From 18 to 21 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: October 2021
See protocol details

Summary

Principal SponsorUniversity of Applied Sciences and Arts Northwestern Switzerland
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 28, 2021

Actual date on which the first participant was enrolled.

The study plans to recruit 5000 young adults aged 18 to 21 representative of the German speaking Swiss population. Participant will be invited to the study by mail. Addresses stem from a Swiss sampling registry ("Stichprobenregister SRPH") and are provided by the Swiss Statistical Office. Access to this address lists is reserved to studies of national interest that are funded by the Swiss National Science foundation. Data collection will be conducted online with a REDCap survey following an accelerated cohort design. After the baseline measurement (w1), three follow ups are planned after 1 year (w2), 2 years (w3) and 3 years (w4), resulting in ages 18 to 24 being covered. The primary outcome will be psychosocial functioning across the study period. 1. Primary objective: The primary objective of the study is to analyse the longitudinal associations between childhood experiences, emotion regulation, social information processing, social support and psychosocial functioning in young adults. * Hypothese 1 is that adverse childhood experiences (ACE) are associated with a higher risk for lower psychosocial functioning in young adulthood and 2) that this association is mediated by deficits in emotion regulation, social information processing and lower social support. * Hypothese 2 is that positive childhood experiences are associated with higher social support, adaptive emotion regulation and high well-being in young adulthood and that good relationships with parents and high social support are a protective factor in the presence of adversities. * Hypothese 3 is that among young adults with ACE, higher social support, seeking professional help and more adaptive coping strategies are associated with a more adaptive psychosocial functioning. Secondary objectives are 2. to examine the effect of childhood experiences on emotion regulation and social information processing. 3. to investigate the effects of emotion regulation and social information processing on the quality of friendships and social support. 4. to analyse the longitudinal associations of childhood experiences, emotion regulation, social information processing, social support and the single variables that constitute the composite score of psychosocial functioning, e.g. well-being, psychosocial distress, risk behaviours. 5. to investigate the associations between ACE, emotion regulation and social information processing and seeking professional support. 6. Further exploratory hypotheses investigate whether there are patterns of ACE which show differential associations with emotion regulation, social information processing, support and psychosocial functioning or single variables of psychosocial functioning.

Official TitleFacing Adverse Childhood Experiences Using New Technologies
NCT05122988
Principal SponsorUniversity of Applied Sciences and Arts Northwestern Switzerland
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

2606 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 21 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Self-ControlEmotional RegulationBehaviorSocial Behavior

Criteria

Inclusion Criteria: * Age 18 to 21, Living in German-speaking Switzerland, Internet Access Exclusion Criteria: * Insufficient mastery of German

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University of Applied Science Northwestern Switzerland

Olten, SwitzerlandOpen University of Applied Science Northwestern Switzerland in Google Maps
CompletedOne Study Center