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Roots for Life Project: Strengthening Mental Health in School Communities

26 de abril de 2026 actualizado por: Universidad de Valparaiso

Pilot Study of a Mental Health Literacy-Based Intervention for Parents and Teachers to Improve the Mental Health of Children in 3rd to 5th Grade in Chile and Ecuador

This pilot study, titled "Roots for Life Project: Strengthening Mental Health in School Communities", aims to evaluate the feasibility and preliminary effectiveness of a mental health literacy (MHL) intervention for teachers and parents to improve the mental health of children aged 8-11 years (3rd to 5th grade) in primary schools located in socially vulnerable areas of Chile and Ecuador.

Child mental health problems represent a major burden worldwide, with high prevalence and a treatment gap exceeding 70% in Latin America. Schools and families play a key role in early detection, yet both often lack the necessary knowledge and confidence to identify mental health difficulties or seek appropriate help. Increasing mental health literacy-defined as knowledge and beliefs that support recognition, management, and prevention of mental health problems-has proven to enhance early help-seeking, reduce stigma, and promote wellbeing.

The project builds upon the prior Chilean FONIS Project SA21I0143, which tested a teacher-focused MHL program and demonstrated improvements in teachers' knowledge, reduced depressive symptoms, and lower burnout levels. The current study extends this work by (1) adding a parent-focused component, (2) evaluating outcomes in children, and (3) implementing the program in two countries to assess cross-cultural feasibility.

This quasi-experimental study will include seven primary schools-five in Chile (Valparaíso, Achao, Curaco de Vélez) and two in Ecuador (Daule). Schools will be randomly assigned within each locality to either intervention or control conditions. Approximately 230 children, their parents/guardians, and teachers will participate. Assessments will be conducted before and after the intervention using validated instruments.

The teacher program consists of six 2-hour participatory workshops covering topics such as self-care, child development, anxiety and depression, suicide prevention, behavioral disorders, autism, and child maltreatment. The parent program includes three 90-minute educational sessions addressing stigma, social support, healthy development, and emotional containment. Both components emphasize experiential learning and culturally adapted materials.

Primary outcome:

Mental health literacy among parents and teachers (MHL Scale).

Secondary outcomes:

Psychological wellbeing of adults (GHQ-12).

Chronic stress levels in children (cortisol in fingernails).

Adverse childhood experiences (ACE questionnaire).

Implementation indicators (acceptability, satisfaction, barriers, facilitators).

Quantitative analyses will compare pre- and post-intervention outcomes and calculate effect sizes. Mediation and moderation models will explore relationships among child, family, and school-level variables. Qualitative data from focus groups with parents and teachers will complement these findings to evaluate feasibility and contextual adaptations.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

This pilot study aims to evaluate the preliminary effectiveness and feasibility of a mental health literacy (MHL) intervention directed at teachers and parents in primary schools (grades 3-5) located in socially vulnerable communities in Chile and Ecuador. The ultimate goal is to improve the mental health and wellbeing of children through enhanced recognition, prevention, and response to mental health needs in school and family environments.

Background and Rationale

Child mental health is a key determinant of overall wellbeing in adulthood. In Latin America, mental disorders among children and adolescents account for a significant disease burden, yet more than 70% of affected children receive no specialized care. Schools are often the first setting where emotional and behavioral problems are detected, but teachers and families frequently lack the necessary knowledge to identify mental health issues or to access appropriate support networks.

Mental health literacy-defined as knowledge and beliefs about mental disorders that aid their recognition, management, or prevention-has proven effective in promoting early detection, help-seeking, and stigma reduction. However, most MHL programs have targeted adolescents, with few focused on primary education or on low- and middle-income countries. This project seeks to fill that gap by implementing and adapting an evidence-informed MHL program for educators and parents in both Chile and Ecuador.

The intervention builds upon the previous FONIS Project SA21I0143, which demonstrated that teacher-focused MHL workshops improved mental health knowledge, reduced depressive symptoms, and lowered burnout.

Study Design

This is a quasi-experimental pilot study with intervention and control schools in both countries. The intervention will be implemented in seven primary schools: five in Chile (Valparaíso, Achao, and Curaco de Vélez) and two in Ecuador (Daule). Randomization will occur at the school level within each locality.

Approximately 230 children (ages 8-11 years) and their parents and teachers will participate. Data will be collected pre- and post-intervention, combining quantitative and qualitative methods.

Intervention

Teacher Program:

Six 2-hour group sessions (12 hours total).

Interactive and experiential methodology: discussion of cases, videos, role-play, and reflective activities.

Topics include: self-care and networks, child development, anxiety and depression, suicide spectrum, ADHD and behavioral disorders, autism spectrum disorder, and child maltreatment.

Parent/Guardian Program:

Three 90-minute workshops.

Topics: stigma and social support, healthy development, warning signs, and emotional containment.

Conducted in schools using participatory and culturally adapted approaches.

Data Collection and Analysis

Baseline data will be collected in April 2025, followed by post-intervention assessment in the second semester of 2025. Quantitative data will be analyzed using paired comparisons and effect size estimation (Cohen's d). Mediation and moderation analyses will explore the roles of family, school, and neighborhood factors. Qualitative data from focus groups with parents and teachers will be thematically analyzed to assess feasibility and contextual factors.

Expected Impact

This pilot will provide foundational evidence on the feasibility, cultural adaptation, and preliminary effectiveness of a community-based MHL program in Latin American primary schools. Expected benefits include:

Improved mental health literacy among parents and teachers.

Early identification and referral of children with emotional or behavioral problems.

Reduced stigma and enhanced school-family collaboration.

Development of a scalable, intersectoral model for child mental health promotion aligned with WHO/PAHO priorities.

Results will inform a future cluster randomized trial and the potential regional expansion of the Roots for Life Project

Tipo de estudio

Intervencionista

Inscripción (Estimado)

200

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Fanny Leyton
  • Número de teléfono: +56 996334590
  • Correo electrónico: fanny.leyton@uv.cl

Ubicaciones de estudio

    • Chiloe
      • Achao, Chiloe, Chile
        • Reclutamiento
        • Servicio Local de Educación (SLEP) Chiloe
        • Contacto:
    • Valparaiso
      • Valparaíso, Valparaiso, Chile, 2581967
        • Reclutamiento
        • Servicio Local de Educación (SLEP)
        • Contacto:
          • Fanny Leyton
          • Número de teléfono: +56 996334590
          • Correo electrónico: fanny.leyton@uv.cl
    • Daule
      • Daule, Daule, Ecuador
        • Reclutamiento
        • Unidad educativa Victoria Torres de Neira
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Descripción

Inclusion Criteria:

Children Participants:

  • Child is enrolled in 3rd, 4th, or 5th grade of primary school
  • Child is under 12 years of age
  • Child's parent or legal guardian has provided written informed consent
  • Child attends a participating public or subsidized school in Valparaíso, Achao, Curaco de Vélez (Chile), or Daule (Ecuador)

Teachers:

  • Works as a teacher in a participating school
  • Teaches students in first or second cycle of primary education (grades 1-6)
  • Voluntarily agrees to participate in the study

Parents/Caregivers:

  • Is the parent or caregiver of a child under 12 years of age
  • Child is enrolled in 3rd, 4th, or 5th grade of primary school
  • Voluntarily agrees to participate in the study

Exclusion Criteria:

Children Participants:

- Child has sensory problems or physical disabilities that prevent completion of surveys

Teachers:

  • Works as educational assistant or in administrative functions only
  • Voluntarily declines to participate in the study

Parents/Caregivers:

  • Child has sensory problems or physical disabilities that prevent completion of surveys
  • Voluntarily declines to participate in the study

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Child Mental health Literacy Program
School staff and parents/caregivers from four schools will receive mental health literacy training through a multicomponent intervention.
School staff and parents/caregivers from four schools will receive mental health literacy training through a multicomponent intervention. Educators will attend 6 in-person modules (120 minutes each, totaling 12 contact hours) covering care and self-care, healthy development, and mental health problems including anxiety, depression, suicidal spectrum, ADHD, conduct disorders, autism spectrum, and child maltreatment. Parents/caregivers will participate in 3 in-person modules (90 minutes each, totaling 4.5 contact hours) addressing stigma, support networks, healthy development, warning signs, and emotional containment. Both components use participatory methodologies including case discussions, audiovisual resources, and group reflection to create a coordinated support network for children's mental health.
Sin intervención: Control
School staff and parents/caregivers from four schools will continue with their usual practices without receiving mental health literacy training.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Children's Mental Health Problems Measured by SDQ
Periodo de tiempo: Baseline and 16 weeks
Change in the Total Difficulties Score (TDS) of the Strengths and Difficulties Questionnaire (SDQ) completed by parents/caregivers and teachers. The SDQ assesses emotional problems, conduct problems, hyperactivity/inattention, and peer relationship problems. The Total Difficulties Score is obtained by summing four of the five dimensions (excluding prosocial behavior). Scores range from 0 to 40, with higher scores indicating greater difficulties. Scores from parent and teacher reports will be analyzed.
Baseline and 16 weeks
Change in Teachers' Emotional Well-being
Periodo de tiempo: Baseline and 16 weeks
Change in teachers' mental health problems measured with the 12-item General Health Questionnaire (GHQ-12). The GHQ-12 is a screening instrument for detecting possible mental disorders. It consists of 12 questions. The best cut-off point validated in Chile is between 4/5 points to classify as possible mental disorder. Higher scores indicate greater likelihood of presenting mental health problems.
Baseline and 16 weeks
Change in Parents/Caregivers' Emotional Well-being
Periodo de tiempo: Baseline and 16 weeks
Change in parents and caregivers' mental health problems measured with the 12-item General Health Questionnaire (GHQ-12). The GHQ-12 is a screening instrument for detecting possible mental disorders. It consists of 12 questions. The best cut-off point validated in Chile is between 4/5 points to classify as possible mental disorder. Higher scores indicate greater likelihood of presenting mental health problems.
Baseline and 16 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Teachers' Mental Health Literacy
Periodo de tiempo: Baseline and 16 weeks
Change in mental health literacy level measured with the Mental Health Literacy Scale validated in Chile. This scale assesses knowledge about identification and treatment of mental disorders, help-seeking, and stigma reduction. The scale has 5 sections with 12 items. Higher scores indicate greater level of mental health literacy.
Baseline and 16 weeks
Change in Parents/Caregivers' Mental Health Literacy
Periodo de tiempo: Baseline and 16 weeks
Change in mental health literacy level measured with the Mental Health Literacy Scale validated in Chile. This scale assesses knowledge about identification and treatment of mental disorders, help-seeking, and stigma reduction. The scale has 5 sections with 12 items. Higher scores indicate greater level of mental health literacy.
Baseline and 16 weeks
Intervention Feasibility Assessed by Teachers' Retention Rate
Periodo de tiempo: At program completion (up to 16 weeks).
Feasibility will be assessed as the percentage of teachers who complete the mental health literacy program (attendance at all six sessions) among those who initiate the program. The denominator is the number of teachers who attend at least one session, and the numerator is the number who attend all six sessions of the program.
At program completion (up to 16 weeks).
Intervention Feasibility Assessed by Parents/Caregivers' Retention Rate
Periodo de tiempo: At program completion (up to 16 weeks)
Feasibility measured by the percentage of parents and caregivers who complete the mental health literacy program (attend all 3 sessions of 90 minutes) among those who started the program. The denominator is the number of parents/caregivers who attend at least one session, and the numerator is the number who attend all three sessions. A higher retention rate indicates better feasibility.
At program completion (up to 16 weeks)
Teachers' Satisfaction with the Intervention Assessed by Likert Survey
Periodo de tiempo: After sessions 1, 2, 3, 4, 5, and 6 (up to 16 weeks)
Teachers' satisfaction with each module of the intervention, measured through a study-specific survey with Likert-type questions (scale from 1 to 5) administered after each workshop session. The survey also includes open-ended questions about valued aspects and suggestions for improvement. Higher scores indicate greater satisfaction. Scale: 1 (minimum satisfaction) to 5 (maximum satisfaction).
After sessions 1, 2, 3, 4, 5, and 6 (up to 16 weeks)
Parents/Caregivers' Satisfaction with the Intervention Assessed by Likert Survey
Periodo de tiempo: After sessions 1, 2, and 3 (up to 16 weeks)
Parents and caregivers' satisfaction with each module of the intervention, measured through a study-specific survey with Likert-type questions (scale from 1 to 5) administered after each workshop session. The survey also includes open-ended questions about valued aspects and suggestions for improvement. Higher scores indicate greater satisfaction. Scale: 1 (minimum satisfaction) to 5 (maximum satisfaction).
After sessions 1, 2, and 3 (up to 16 weeks)
Change in Stress Reactivity Measured by Nail Cortisol
Periodo de tiempo: Baseline and 16 weeks
Change in accumulated cortisol levels measured in children's nail samples. Nail cortisol reflects chronic stress exposure during the 4-5 months prior to sample collection. Results are expressed in picograms of cortisol per milligram of nail (pg/mg). Higher levels indicate greater chronic stress exposure or allostatic overload.
Baseline and 16 weeks

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de marzo de 2025

Finalización primaria (Estimado)

31 de mayo de 2026

Finalización del estudio (Estimado)

31 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

10 de diciembre de 2025

Primero enviado que cumplió con los criterios de control de calidad

26 de abril de 2026

Publicado por primera vez (Actual)

4 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

26 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • ORD842

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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