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Who Are You (WAY) Online Social and Emotional Learning Program for Adolescents (WAY)

22 août 2026 mis à jour par: Melih Dikmen

A Randomized Controlled Trial of a Digital Social and Emotional Learning Program for Adolescents: Effects on Social-Emotional Functioning and Academic Achievement

This study evaluated the Who Are You (WAY) program, a 10-week online social and emotional learning program designed for adolescents. The program aims to help young people better understand and manage emotions, regulate their behavior, stay motivated in learning, cope with stress, and develop goal-directed skills.

A total of 120 adolescents took part in the study, including 60 middle-school students and 60 high-school students. Within each educational group, participants were randomly assigned either to the WAY program or to a waitlist group that continued with their usual education. The WAY program combined weekly one-to-one online sessions with structured independent learning activities.

Participants completed assessments before and after the 10-week period. The main outcomes were self-regulation, emotional intelligence, academic motivation, and perceived stress. Academic achievement was also assessed as a secondary educational outcome.

The study tested the hypothesis that adolescents assigned to the WAY program would show greater improvement in social-emotional functioning than adolescents assigned to the waitlist condition.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

This was a two-arm, parallel-group, assessor-blinded, waitlist-controlled randomized trial conducted with two developmentally distinct educational cohorts in Türkiye. Middle-school and high-school participants were randomized separately within cohort in a 1:1 ratio to either the WAY intervention or a waitlist control condition.

WAY was a manualized, digitally supported social and emotional learning intervention delivered over 10 consecutive weeks. Each weekly module included an individual synchronous online session supplemented by structured asynchronous activities. The program addressed self-awareness, emotional understanding and regulation, academic motivation, goal setting, planning, self-monitoring, stress management, adaptive coping, empathy, communication, and maintenance of acquired skills.

Participants in the waitlist condition continued their usual education during the evaluation period and were offered access to the WAY program after completion of post-intervention assessments.

Baseline assessments were completed before randomization, and post-intervention assessments were administered within one week after completion of the intervention period. The four prespecified primary outcome domains were self-regulation, trait emotional intelligence, academic motivation, and perceived stress. Academic achievement was prespecified as a secondary educational outcome. Outcomes were evaluated separately within the middle-school and high-school cohorts.

The trial was completed before registration on ClinicalTrials.gov and is therefore being registered retrospectively.

Type d'étude

Interventionnel

Inscription (Réel)

120

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Enrollment in Grades 5-12.
  • Sufficient proficiency in Turkish to understand the program content and complete the study measures.
  • Reliable internet access and access to an appropriate digital device for participation in the online program.
  • Ability to engage with the program and complete the study measures independently, with reasonable support where required.
  • Written informed consent from a parent or legal guardian and written assent from the adolescent.

Exclusion Criteria:

  • Concurrent participation in another structured social and emotional learning program.
  • A cognitive, sensory, linguistic, or functional difficulty that prevented meaningful participation or independent completion of the study measures despite reasonable accommodations.
  • An acute psychological crisis or serious risk requiring immediate professional assessment or clinical support.
  • Failure to complete the baseline assessment or withdrawal before randomization.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: WAY Intervention
Participants assigned to this arm received the 10-week Who Are You (WAY) social and emotional learning program in addition to their usual education. The program included one individual synchronous online session per week, followed by structured asynchronous learning activities. Each weekly module comprised approximately 30 minutes of synchronous instruction and 15-20 minutes of asynchronous activities.
Comportemental: Who Are You (WAY) Social and Emotional Learning Program
WAY is a manualized, digitally supported social and emotional learning program designed for adolescents. It was delivered individually over 10 consecutive weeks. Each weekly module combined a synchronous online session with structured asynchronous activities. The program addressed self-awareness, emotional understanding and regulation, academic motivation, goal setting, planning, self-monitoring, stress management, adaptive coping, empathy, communication, collaborative problem solving, and maintenance of acquired skills. Sessions used guided discussion, reflective questioning, experiential activities, structured exercises, individualized reflection, and goal setting.
Aucune intervention: Waitlist Control
Participants assigned to this arm continued their usual school education and did not receive WAY sessions, facilitator contact, or intervention materials during the 10-week evaluation period. They were offered access to the WAY program after completion of the post-intervention assessment.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change From Baseline in Perceived Self-Regulation Scale Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Self-regulation in the middle-school cohort was assessed using the 16-item Perceived Self-Regulation Scale. Items are rated on a 5-point Likert-type scale. Total scores are calculated by summing item responses, with higher scores indicating greater perceived self-regulatory capacity.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Self-Regulation Scale for Adolescents Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Self-regulation in the high-school cohort was assessed using the 11-item Self-Regulation Scale for Adolescents. The scale assesses goal setting, planning, monitoring, emotional awareness, and behavioral control using a 5-point response format. Higher total scores indicate greater self-regulatory competence.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Trait Emotional Intelligence Questionnaire-Adolescent Short Form Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Trait emotional intelligence was assessed in both cohorts using the 15-item Trait Emotional Intelligence Questionnaire-Adolescent Short Form (TEIQue-ASF). Items are rated on a 7-point scale. Negatively worded items are reverse scored, and higher total scores indicate greater perceived emotional competence.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Academic Motivation Scale Score in Middle-School Studen
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Academic motivation in the middle-school cohort was assessed using the 28-item Turkish adaptation of the Academic Motivation Scale. Items are rated on a 7-point scale. Total scores are calculated after appropriate reverse scoring, with higher scores indicating stronger academic motivation.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Academic Motivation Scale Score in High-School Students
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Academic motivation in the high-school cohort was assessed using the 22-item Turkish Academic Motivation Scale. Items assess intrinsic motivation, extrinsic motivation, and amotivation and are rated on a 7-point scale. Higher total scores indicate stronger academic motivation after appropriate reverse scoring.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Perceived Stress Scale for Children Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Perceived stress in the middle-school cohort was assessed using the 9-item Perceived Stress Scale for Children. Items are rated on a 4-point frequency scale. Total scores are calculated by summing item responses, with higher scores indicating greater perceived stress.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in Perceived Stress Scale
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Perceived stress in the high-school cohort was assessed using the 10-item Perceived Stress Scale (PSS-10). Items are rated from 0 (Never) to 4 (Very often). Positively worded items are reverse scored before calculating the total score, with higher scores indicating greater perceived stress.
Baseline and post-intervention, within 1 week after completion of the 10-week program

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change From Baseline in Middle School Academic Achievement Test Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Academic achievement in the middle-school cohort was assessed using the 75-item Middle School Academic Achievement Test (MS-AAT), covering Turkish language, social studies, mathematics, and science. Items are scored 1 for a correct response and 0 for an incorrect or omitted response, with higher total scores indicating greater academic achievement.
Baseline and post-intervention, within 1 week after completion of the 10-week program
Change From Baseline in High School Academic Achievement Test Score
Délai: Baseline and post-intervention, within 1 week after completion of the 10-week program
Academic achievement in the high-school cohort was assessed using the 80-item High School Academic Achievement Test (HS-AAT), covering curriculum-based academic domains. Items are scored 1 for a correct response and 0 for an incorrect or omitted response, with higher total scores indicating greater academic achievement.
Baseline and post-intervention, within 1 week after completion of the 10-week program

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Melih Dikmen

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

15 décembre 2025

Achèvement primaire (Réel)

27 mars 2026

Achèvement de l'étude (Réel)

27 mars 2026

Dates d'inscription aux études

Première soumission

18 août 2026

Première soumission répondant aux critères de contrôle qualité

18 août 2026

Première publication (Réel)

24 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

25 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

22 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Mots clés

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • WAY-RCT-01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

De-identified individual participant data underlying the results reported in the publication will be shared together with the corresponding data dictionary and analytic code.

Délai de partage IPD

Data will be available following publication of the primary study report and will remain available without a predefined end date.

Critères d'accès au partage IPD

Data will be publicly available without individual application or approval requirements through an open research repository for research and verification purposes.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • ANALYTIC_CODE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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