A Validation Study of the Neuro-cognitive Emotion Monitoring-Intervention (NEMO-I) Application in Adolescents

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-18
SponsorSeoul Women's University

About this trial

This study aims to evaluate the validity and effectiveness of NEMO-I (Neuro-cognitive Emotion Monitoring-Intervention), a mobile application designed to help adolescents monitor and manage their cognitive and emotional functioning in everyday settings. NEMO-I delivers evidence-based psychological techniques-such as mindfulness, self-regulation training, and emotion monitoring-in a gamified format consisting of seven brief activities that users can complete at home in about 10 minutes each.

A total of 140 middle and high school students will participate. Participants will complete standardized neuropsychological and psychological assessments before and after the intervention period. During the 21-day intervention period, participants will use the NEMO-I application at home each day at their convenience (a minimum of 10 minutes per day is recommended). By comparing pre- and post-intervention assessment results, this study seeks to determine whether the application produces meaningful benefits for adolescent mental health and to establish its suitability as a digital mental health tool.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Middle or high school students currently enrolled in school

Using an Android-based smartphone

Voluntary agreement to participate, with consent from a legal guardian

Disqualifiers

Borderline intellectual functioning or intellectual disability (IQ below 80)

Visual or hearing impairment

Prior diagnosis of intellectual, visual, or hearing impairment

Trial design

Design model

Single group

Treatments tested in this trial

  • NEMO-I (Neuro-cognitive Emotion Monitoring-Intervention)

    Behavioral

    NEMO-I is a mobile application that delivers evidence-based psychological techniques in a gamified format. It consists of seven brief activities-including facial expression imitation, singing, breathing and stretching with nature sounds, reading tips for everyday concerns, rhythm-based instrument play, room decoration, and mindfulness-each designed to be completed at home in about 10 minutes. Participants use the application daily during the 21-day intervention period, at their convenience, with a recommended minimum of 10 minutes per day.

Treatment groups

140 Participants
are divided into 1 treatment group
Group A: NEMO-I Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in depressive symptoms

Depressive symptoms are measured using the Beck Depression Inventory-II (BDI-II), a 21-item self-report questionnaire. Total scores range from 0 to 63, with higher scores indicating more severe depressive symptoms. Change is assessed by comparing pre- and post-intervention scores.

Time frame
Baseline (pre-intervention) and after the 21-day intervention period
2

Change in inhibitory control (Color-Word Stroop Test, CWST)

Inhibitory control is assessed using the Color-Word Stroop Test (CWST), which measures the efficiency of the frontal-lobe inhibition process. Performance is indexed by response time and error rate under the color-word interference condition. Change is assessed by comparing pre- and post-intervention performance.

Time frame
Baseline(pre-intervention) and after the 21-day intervention period
3

Change in anxiety symptoms

Anxiety symptoms are measured using the Beck Anxiety Inventory (BAI), a 21-item self-report questionnaire assessing the severity of anxiety-related symptoms. Higher scores indicate greater anxiety. Change is assessed by comparing pre- and post-intervention scores.

Time frame
Baseline(pre-intervention) and after the 21-day intervention period
4

Change in neuro-cognitive and emotional function (NEMO-A)

Neuro-cognitive and emotional function is assessed using the NEMO-A (Neuro-cognitive Emotion Monitoring-Assessment) application, a tablet-based, game-format assessment consisting of five subtasks. It measures domains including sustained attention, working memory, emotional sensitivity, emotion processing and recognition, audiovisual emotional integration, cognitive control, and executive function. Performance is indexed by accuracy and response time, and change is assessed by comparing pre- and post-intervention performance.

Time frame
Baseline (pre-intervention) and after the 21-day intervention period

Secondary outcomes

1

Change in subjective stress

Subjective stress is measured using a Visual Analog Scale (VAS), on which participants rate their current perceived stress level from 1 (no stress) to 10 (extreme stress).

Time frame
Baseline (pre-intervention) and after the 21-day intervention period
2

Change in daily stress

Daily stress is measured using a 26-item self-report scale assessing stress experienced in everyday domains such as parents, school, academics, peer relationships, appearance, and finances, rated on a 5-point Likert scale.

Time frame
Baseline(pre-intervention) and after the 21-day intervention period
3

Change in alexithymia

Difficulty identifying and describing one's own emotions is measured using the Korean version of the 20-item Toronto Alexithymia Scale (TAS-20K), rated on a 5-point Likert scale.

Time frame
Baseline (pre-intervention) and after the 21-day intervention period
4

Change in executive function difficulties (self-report)

Self-reported executive function difficulties are measured using the Brief Self-Report Questionnaire of Executive Function Difficulty for children and adolescents (40 items), rated on a 3-point Likert scale.

Time frame
Baseline (pre-intervention) and after the 21-day intervention period

Other outcomes

Sponsors and contacts

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Seoul Women's University

Lead sponsor

Korea Health Industry Development Institute

Collaborator

Ministry of Health & Welfare, Korea

Collaborator

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