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Enrolling by invitation NCT06954064

The Student Living Lab: Intensive Longitudinal ESM Study for DP of ERFs to Stress in AYAs

Observational Emotional Resilience

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention will be applied..
Who it may be relevant to
Registry conditions: Emotional Resilience. Basic parameters: 10 years — 24 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Romania
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Digital Phenotyping of Emotional Resilience Factors to Stress in Adolescents and Young Adults: a Longitudinal Ecological Approach

Overview

This study aims at collecting continuous mobile-based devices data for determining emotional resilience factors and childhood abuse load profiles for stress and mental health problems.

Detailed description

Participants included in this study (age range = 10-24, G\*power estimated N = 255) will complete a set of questionnaires on constructs related to mental health and resilience, creating a digital phenotype based on individual profiles and investigating the dynamics between variables over a months' period.

Interventions

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

Primary outcome measures

  • Resilience factors [Time frame: One month, weekly (5 administrations)]
  • Mental Health [Time frame: One month, weekly (5 administrations)]

Eligibility criteria

Inclusion criteria

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

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Ecologic or community

Study locations

Romania · 1 center
  • Babes-Bolyai University — Cluj-Napoca

Identifiers

NCT: NCT06954064 · REThinkRESILIENT-DP

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗