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Emotional ResilienceNCT06986928

A Network Analysis on the Role of Specific ER Abilities as ERFs for Distress and Mental Health, in Relation to CAs Exposure in the AYAs

An observational study of Emotional Resilience, run by Babes-Bolyai University at 1 site in Romania.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This activity will aim to compare the network of emotional resilience factors and stress in adolescents and young adults depending on the childhood abuse exposure (considered moderator), using a network analysis approach. Read more about this study

Who is it for?
Ages 10 to 24 yearsHealthy volunteers can take part
Conditions the study is for
Emotional Resilience
How many people
370 participants
Where
1 siteRomania
Study dates
20 Feb 2025to 30 Jun 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 24 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Study population: School- and university-aged students recruited from educational institutions in Cluj-Napoca.

Who may be able to join

  • adolescents and young adults between 10 and 24 years old provided with written parental consent where applicable

Who cannot join

  • intellectual disability or physical limitations precluded the use of the computer program

Trial locations and contacts

1 site in 1 country.

Romania1 site
  • Babes-Bolyai University

    Cluj-Napoca, Cluj, 400015

Other trials in Romania

About this study

Official title: A Network Analysis on the Role of Specific Emotion Regulation Abilities as Emotional Resilience Factors for Distress and Mental Health, in Relation to Childhood Abuse Exposure in Adolescents and Young Adults

This activity will aim to compare the network of emotional resilience factors and stress in adolescents and young adults depending on the childhood abuse exposure (considered moderator), using a network analysis approach.

Read the detailed description

Participants included in this study (age range = 10-24, G*power estimated N = 349) will complete a set of questionnaires on constructs that are focusing on or closely related to resilience and mental health, in order to investigate the dynamics of emotional resilience factors in relation to mental health outcomes such as anxiety and depression, taking into account the moderating effects of childhood abuse exposure.

Being tested
No intervention will be applied.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No intervention will be applied.Other

    No intervention will be applied.

  • No intervention will be applied.Other

    No intervention will be implemented in this study, as the questionnaires will serve an exploratory purpose.

Study groups in NCT06986928
Study groupRoleWhat they receive
Adolescents and young adultsAdolescents and young adults will be recruited from various schools and university programs in Cluj-Napoca.
Receives: Other: No intervention will be applied.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Childhood Trauma Exposure

    Childhood Trauma Screener (CTS)

    Measured: Baseline

  2. Emotion regulation abilities

    The REThink Life game-based emotion regulation abilities will be assessed using a scenario of social exclusion and measuring the use of using different emotion regulation strategies.

    Measured: Baseline

  3. Emotional and behavioral difficulties

    Strengths and Difficulties Questionnaire (SDQ)

    Measured: Baseline

  4. Stress

    Adolescence Stress Scale (ADOSS)

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 May 2025
  2. Study start20 Feb 2025
  3. Primary completion10 Jun 2025
  4. Study completion30 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrolment
370 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06986928
Sponsor's protocol ID
REThinkRESILIENT-Network
Status last verified
Aug 2025
First submitted
24 Apr 2025
Last updated
28 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Emotional Resilience, run by Babes-Bolyai University at 1 site in Romania.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Romania. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Childhood Trauma Exposure (time frame: Baseline). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Aug 2025.

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