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Emotional Intelligence Intervention to Improve Mental Well-Being of Adolescents With Emotional Distress (BEAM)

Emotional Intelligence Intervention to Improve Mental Well-Being of Adolescents With Emotional Distress (BEAM): Study Protocol for a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06713460
Acronym
BEAM
Enrollment
104
Registered
2024-12-03
Start date
2025-04-07
Completion date
2026-12-30
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emotional Distress

Keywords

Mental Well-being, Emotional Intelligence, Emotional Distress, Adolescents

Brief summary

The goal of this clinical trial is to assess the effectiveness of a multicomponent intervention in adolescents with emotional distress. The main question it aims to answer is: Does the intervention increase mental well-being, emotional resilience, and emocional intelligence in adolescents with emotional distress? Participants will: • Participate in a multi-component intervention for 9 weeks at school.

Detailed description

Background:Adolescence involves biological, psychological and social transformations that increase vulnerability to mental health problems. Emotional intelligence is a protective factor that improves mental well-being. Given the sensitivity of adolescence to mental health disorders, emotional intelligence emerges as a valuable tool for promoting mental well-being.The investigators hypothesize that adolescents aged 14-16 with emotional distress who receive the multicomponent intervention based on emotional intelligence will obtain better scores on the Warwick-Edinburgh Mental Well-being Scale compared to the control group, after the intervention and at 24 weeks post-intervention. Method :The study is a Randomized Controlled Trial (RCT). The participants and their parents will sign an agreement to participate in the study and will be randomly allocated in control and intervention groups by external researcher using a computer-generated random number. The intervention will be conducted in a school setting during the 2025-2026 academic year. It will comprise a multicomponent program consisting of nine sessions, each lasting 55 minutes, addressing various topics related to emotional intelligence. Data will be collected from April 2026 to december 2026."Three psychometric scales will be used: Warwick-Edinburgh Mental Wellbeing Scale (WEMWB), Trait Meta-Mood Scale (TMMS-24) and Child Youth Resilience Measure (CYRM-32), with measurements before the intervention (T0), 9 (T1) and 24 weeks follow-up (T2).The group receiving the intervention is expected to show improvements in emotional well-being, emotional intelligence and resilience compared to the control group. Accepting an alpha risk of 0.05 and a beta risk of 0.20 in a bilateral contrast, 52 subjects in the first group and 52 in the second group are required to detect a difference equal to or greater than 5 units on the WEMWBS scale. A common standard deviation of 6.8 is assumed. A loss to follow-up rate of 0.1 (10%) and a correlation between observations of 0.4 was estimated.

Interventions

BEHAVIORALBEAM

Multicomponent intervention

Sponsors

Consorci Sanitari de Terrassa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

Due to the difficulty of masking conditions, the groups and participating personnel (research team) will not be blinded.

Intervention model description

Participants will be randomly assigned to either the control or intervention group by an external investigator through computer-generated random numbers.

Eligibility

Sex/Gender
ALL
Age
14 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

* Adolescents with emotional distress scores on the Warwick-Edinburgh Mental Well- being Scale. * Adolescents aged 14-16 ( in 9th Grade). * Informed consent form signed (by adolescents and their parent or legal guardian)

Exclusion criteria

* Physical illnesses that prevent attendance at scheduled sessions, severe mental disorders (such as Autism Spectrum Disorder, major depression, schizophrenia). * No comprehension of the language * Lack of consent from the adolescents or their parents or legal guardians

Design outcomes

Primary

MeasureTime frameDescription
Improve well-beingBaseline (T0), post-intervention (9 weeks) (T1), and 24 weeks follow-up (T2)Changes in level of well-being using the Warwick-Edinburgh Mental Well-Being Scale (WEMWBS). Values range from 14 to 70 . Higher scores, better outcome.

Secondary

MeasureTime frameDescription
Increased resilienceBaseline (T0), post-intervention (9 weeks) (T1), and 24 weeks follow-up (T2)Changes in level of resilience using the Child Youth Resilience Measure -32. Values range from 32 to 160 . Higher scores, better outcome.
Increase emotional intelligenceBaseline (T0), post-intervention (9 weeks) (T1), and 24 weeks follow-up (T2)Changes in level of emotional intelligence using the Trait Meta-Mood Scale (TMMS). The TMMS-24 contains three key dimensions of EI with 8 items each: Emotional Attention: Adequate values: Males (22 to 32); Females (25 to 35); Emotional clarity: excellent values: Males (\> 36); Females (\>35), and Emotional repair: excellent values: Men (\> 36); Women (\>35)).

Countries

Spain

Contacts

PRINCIPAL_INVESTIGATORMaria Llistosella, PhD

Primary Health Care, Consorci Sanitari de Terrassa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026