Emotional ResilienceNCT06954064
The Student Living Lab: Intensive Longitudinal ESM Study for DP of ERFs to Stress in AYAs
An observational study of Emotional Resilience, run by Babes-Bolyai University at 1 site in Romania.
Trial summary
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. 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
- 343 participants
- Where
- 1 siteRomania
- Study dates
- 10 Mar 2025to 30 Jun 2026
- 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.
About this study
Official title: 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.
Read the 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.
- Conditions
- Emotional Resilience
- 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 implemented in this study, as the questionnaires will serve an exploratory purpose.
| Study group | Role | What they receive |
|---|---|---|
| Adolescents and young adults | Adolescents 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.
Resilience factors
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.
Measured: One month, weekly (5 administrations)
Mental Health
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.
Measured: One month, weekly (5 administrations)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 May 2025
- Study start10 Mar 2025
- Primary completion30 Jun 2026
- Study completion30 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Emotional ResilienceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Other
- Enrolment
- 343 participants (actual)
Sponsor and investigators
- Lead sponsor
- Babes-Bolyai University
- Sponsor type
- University, hospital or other
- Collaborators
- The Executive Agency for Higher Education, Research, Development and Innovation Funding
- Responsible party
- Principal investigator, Oana David, Babes-Bolyai University
- Investigators
- Oana A. David, Ph.D, Principal investigator, Babes-Bolyai University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06954064
- Sponsor's protocol ID
- REThinkRESILIENT-DP
- Status last verified
- Oct 2026
- First submitted
- 24 Apr 2025
- Last updated
- 13 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Digital Phenotyping of Emotional Resilience Factors to Stress in Adolescents and Young Adults: a Longitudinal Ecological Approach
- ClinicalTrials.gov ID
- NCT06954064
- Acronym / sponsor ID
- REThinkRESILIENT-DP
- Conditions
- Emotional Resilience
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 343 participants (actual)
- Lead sponsor
- Babes-Bolyai UniversityUniversity, hospital or other
- Collaborators
- The Executive Agency for Higher Education, Research, Development and Innovation Funding
- Study start
- 10 Mar 2025 (actual)
- Primary completion
- 30 Jun 2026 (actual)
- Study completion
- 30 Jun 2026 (actual)
- First posted
- 1 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Ecologic or community
- Time perspective
- Other
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Adolescents and young adults | – | Other: No intervention will be applied.Adolescents and young adults will be recruited from various schools and university programs in Cluj-Napoca. |
Who may qualify
- Ages
- 10 to 24 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
- Study population
- School- and university-aged students recruited from educational institutions in Cluj-Napoca.
Key inclusion criteria (1 listed)
- adolescents and young adults between 10 and 24 years old provided with written parental consent where applicable
Key exclusion criteria (1 listed)
- intellectual disability or physical limitations precluded the use of the computer program
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No intervention will be applied.No intervention will be implemented in this study, as the questionnaires will serve an exploratory purpose. | Other | Adolescents and young adults |
Primary outcome
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.
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Oct 2026.
- Individual participant dataSharing planned: No
Related trials for Emotional Resilience
Active, not recruiting
Emotional Well-being and Measures of Healthy Aging
Aging, Aging, Healthy
Recruiting
The Coma Family Program (COMA-F): A Resilience Program for Caregivers of Patients With Severe Acute Brain Injury
Caregiver Distress, Emotional Distress
Not yet recruiting
Mandala-Based Intervention in Pregnancy
Perception of Traumatic Childbirth, Psychological Resilience
Recruiting
Psychological Prehabilitation for Complex Gastrointestinal Surgery
Post-traumatic Stress Symptoms, Anxiety
Active, not recruiting
Online Socio-emotional Dyad Training for Healthcare Students' Well-being and Social Skills
Intervention Condition, Control (Delayed Training) Condition
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Oana A. David, Ph.D principal investigator
Babes-Bolyai University
1 site in 1 country: see every site and its status.
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 13 Oct 2026. 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?
Resilience factors (time frame: One month, weekly (5 administrations)). The study lists 2 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 13 Oct 2026.