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CompletedNCT06878521Updated Mar 12, 2026

Strengthening Emotional Regulation: a Group Intervention With Adolescents

An interventional study of Emotional Regulation Skills in Emotional Regulation, sponsored by Lorena Wenger Amengual. Completed at 1 site in Chile. Open to participants aged 14 Years to 16 Years. Per ClinicalTrials.gov, last updated 2026-03-12.

Sponsored by Lorena Wenger Amengual · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jul 2024, registered Jan 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
69
Allocation
Randomized
Ages
14 Years to 16 Years
Sex
All
01

Study summary

The goal of this clinical trial is to determine the initial efficacy of an emotional regulation skills training (ERST) intervention program in a group of adolescents presenting mild symptoms affecting their ability to regulate emotions. For this purpose, a sample of 1st and 2nd-year high school students (ages 14-16) will be recruited, and the intervention will be conducted on the educational institution's premises during school hours. The main questions it aims to answer are:

Does the ERST intervention reduce symptom levels in adolescents with mild emotional dysregulation? Does the ERST intervention improve emotional regulation skills in adolescents? Researchers will compare pre-intervention (T1) and post-intervention (T2) outcomes, as well as follow-up assessments at 3 months, to evaluate changes in symptom levels and emotional dysregulation. Additionally, a blinded teacher assessment will be conducted at T1 and T2 to evaluate symptom levels.

Participants will:

Attend the ERST intervention sessions during school hours. Complete self-report assessments at four time points (T1, T2, and 3-month follow-up).

Be evaluated by a blinded teacher at T1 and T2.

02

Conditions studied

  • Emotional Regulation

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Keywords

  • Adolescents
  • Emotional regulation
  • Transdiagnostic
  • Transdiagnostic intervention
  • Group intervention
  • Emotion Regulation Skills Training
  • School-based intervention
03

In context

Emotional Regulation

225 studies on the registry are indexed under Emotional Regulation; 122 are open to participants now.

This study's enrollment of 69 is close to the median of 73 across 212 interventional studies indexed under Emotional Regulation.

Browse Emotional Regulation studies →

Lead sponsor

This is the only study on the registry with Lorena Wenger Amengual as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 16 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adolescents in their first or second year of high school.
  • Must be currently enrolled in school.
  • They should be referred for emotional dysregulation issues and require mental health support.
  • They must score above the 75th percentile on the total scale of the SDQ screening tool

Exclusion criteria

Exclusion Criteria:

  • Adolescents who are regularly receiving psychological treatment
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
69 participants (actual)

Study arms

  • Experimental
    Emotional regulation skills training Group

    Participants in this group will receive the emotional regulation skills training (ERST) intervention.

    Other: Emotional Regulation Skills

  • No intervention
    Waitlist Control Group

    Participants in this group will not receive the intervention initially and will be placed on a waitlist. They will receive the same emotional regulation skills training (ERST) intervention after the experimental group has completed the program.

Interventions

  • OtherEmotional Regulation Skills

    This intervention is inspired by and incorporates elements of Dialectical Behavior Therapy (DBT). It consists of eight weekly group sessions, each lasting approximately 1.5 to 2 hours, held on school premises. Each group includes 8 to 10 adolescents. The sessions are facilitated by two psychologists and/or senior psychology students who have been specifically trained to deliver the intervention. The sessions focus on developing various emotional regulation skills, which participants are encouraged to practice both during and between sessions. Some of the key skills covered include Mindfulness, Wise Mind, and Problem-Solving, among others.

06

What researchers measure

Primary outcomes

  1. Change from Baseline in Emotional Dysregulation Over Time Compared to the Control Group

    Emotional dysregulation is measured using the "Difficulty in Emotion Regulation Scale" (DERS-E). This self-report questionnaire is administered to participants at baseline (Day 0), at the end of the intervention (Month 2), and three months later for follow-up (Month 3).

    Time frame: Day 0 = during enrollment, Month 2 = immediately after the experimental group completes the intervention, and Month 3 = three months later for follow-up

  2. Change from Baseline in Psychological Functioning screening Over Time Compared to the Control Group

    Psychological functioning screening is assessed using the "Strengths and Difficulties Questionnaire" (SDQ) (self-report version), which measures emotional and behavioral difficulties. The minimum value for the general difficulty scale is 0, and the maximum value is 40, where higher scores indicate worse psychological functioning. This questionnaire is administered to participants at baseline (Day 0), at the end of the intervention (Month 2), and three months later for follow-up (Month 3).

    Time frame: Day 0 = during enrollment, Month 2 = immediately after the experimental group completes the intervention, and Month 3 = three months later for follow-up

  3. Change from Baseline in Anxiety Symptoms Over Time Compared to the Control Group

    Anxiety Symptoms are assessed using the "Generalized Anxiety Disorder 7" (GAD-7), which measures the presence and severity of anxiety symptoms. The minimum value for the scale is 0, and the maximum value is 21, where higher scores indicate worse anxiety symptoms. This questionnaires is administered to participants at baseline (Day 0), at the end of the intervention (Month 2), and three months later for follow-up (Month 3).

    Time frame: Day 0 = during enrollment, Month 2 = immediately after the experimental group completes the intervention, and Month 3 = three months later for follow-up

  4. Change from Baseline in Depressive Symptoms Over Time Compared to the Control Group

    The evaluates the severity of depressive symptoms. Depressive Symptoms are assessed using the "Patient Health Questionnaire 9" (PHQ-9), which measures the severity of depressive symptoms. The minimum value for the scale is 0, and the maximum value is 27, where higher scores indicate worse depressive symptoms. This questionnaires is administered to participants at baseline (Day 0), at the end of the intervention (Month 2), and three months later for follow-up (Month 3).

    Time frame: Day 0 = during enrollment, Month 2 = immediately after the experimental group completes the intervention, and Month 3 = three months later for follow-up

Secondary outcomes

  1. Change from Baseline in Clinical Symptoms Over Time Compared to the Control Group, with Masking in the Evaluation Process

    A blinded teacher assessment will be conducted at baseline (Day 0), at the end of the intervention (Month 2) to evaluate symptom levels in both groups, using the "Strengths and Difficulties Questionnaire: Teacher-rated" (SDQ). The minimum value for the general difficulty scale is 0, and the maximum value is 40, where higher scores indicate worse psychological functioning.

    Time frame: Day 0 = during enrollment, Month 2 = immediately after the experimental group completes the intervention

07

Study locations

1 site
  • Universidad de La Frontera
    Temuco, Chile
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06878521
Lead sponsor
Lorena Wenger Amengual
Collaborators
Agencia Nacional de Investigación y Desarrollo
Responsible party
Lorena Wenger Amengual (Principal Investigator, Universidad de La Frontera) — Sponsor-investigator
First posted
Mar 17, 2025
Start date
Jul 12, 2024
Primary completion
Dec 9, 2025
Completion
Dec 9, 2025
Last update
Mar 12, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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