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

August 27, 2025 updated by: Oana David, Babes-Bolyai University

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

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.

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

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.

Study Type

Observational

Enrollment (Estimated)

255

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Romania
    • Cluj
      • Cluj-Napoca, Cluj, Romania, 400015
        • Babes-Bolyai University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

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

Description

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

Study Plan

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

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Adolescents and young adults
Adolescents and young adults will be recruited from various schools and university programs in Cluj-Napoca.
Other: No intervention will be applied.
No intervention will be implemented in this study, as the questionnaires will serve an exploratory purpose.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Resilience factors
Time Frame: One month, weekly (5 administrations)
The Rugged Resilience Measure (RRM) is a 10-item scale measuring internal essential qualities associated with resilience, using 5-point Likert scales for scoring, from 1 = not at all to 5 = a lot.
One month, weekly (5 administrations)
Mental Health
Time Frame: One month, weekly (5 administrations)
The Depression, Anxiety, and Stress Scales (DASS-21) are comprised of 21 items measuring the frequency of symptoms that can be bothering individuals in the sphere of depression, anxiety and stress. The scoring is based on Likert scales from 0 = Never to 4 = Almost always.
One month, weekly (5 administrations)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Babes-Bolyai University

Collaborators

The Executive Agency for Higher Education, Research, Development and Innovation Funding

Investigators

  • Principal Investigator: Oana A. David, Ph.D, Babes-Bolyai University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 10, 2025

Primary Completion (Estimated)

April 1, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

April 24, 2025

First Submitted That Met QC Criteria

April 24, 2025

First Posted (Actual)

May 1, 2025

Study Record Updates

Last Update Posted (Estimated)

August 28, 2025

Last Update Submitted That Met QC Criteria

August 27, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REThinkRESILIENT-DP

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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