Building Resilience at Schools: Emotional and Biological Assessment and Treatment of Traumatic Stress

Not Applicable

Recruiting

• Conditions: Burn Out; Post Traumatic Stress Disorder; Complex Posttraumatic Stress Disorder; Mental Health Issue; Stress
• Interventions: Behavioral: Start with the Heart Students; Behavioral: Start with the Heart Teachers; Behavioral: Cue Centered Therapy Counselors; Behavioral: Cue Centered Therapy Students; Genetic: iSWAB-DNA

• Registration Number: NCT05701111
• Lead Sponsor: Stanford University

Brief Summary

In the last four years alone, residents of Puerto Rico have experienced a slew of natural disasters including Hurricane Maria in 2017, earthquakes in 2019 and 2020, the continued COVID-19 pandemic from 2020-2022, and most recently Hurricane Fiona. This series of distressing events can lead to an increased need for mental health resources and trauma treatment. Furthermore, the unique single-district structure of the Puerto Rican education system allows for the efficient dissemination of potential interventions and treatment to all students.

The purpose of this study is to examine two treatment conditions for educators and school-aged children in Puerto Rico experiencing burnout, fatigue, and high stress: delivery of a mindfulness-based educator curriculum and, for children who report Post Traumatic Stress Disorder (PTSD) symptomatology, delivery of the mindfulness curriculum with the additional intervention of Cue-Centered Therapy (CCT). The study has two aims: 1) To assess the efficacy of the mindfulness curriculum and of CCT in a population of students, counselors, and teachers, characterized by high stress over the last few years of natural disasters and pandemic challenges and 2) To identify genetic contributions to resilience by analyzing gene expression in students before and after the intervention.

The overarching goals of the investigators' research collaboration are to improve educators' psychological well-being and children's socioemotional development when faced with high stress and adversity and to improve mental health clinicians' competence and confidence in treating children exposed to trauma by training them in CCT. The investigators' research will identify critical biopsychosocial components responsible for the cognitive, behavioral, and emotional improvement and effective implementation strategies in a large but geographically dispersed school district. The knowledge base that will result from this study will inform the implementation of trauma-informed care in school settings and with populations experiencing stress and adversity, and contribute to the investigators' understanding of the underlying biology of these interventions to provide a rationale for further development and dissemination.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-12-19
• Study First Submitted QC: 2023-01-24
• Study First Posted: 2023-01-27
• Study Start: 2024-02-23
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-14
• Last Update Posted: 2025-04-17
• Primary Completion: 2027-05
• Study Completion: 2027-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 80800

Inclusion Criteria

1. Teachers and students at a participating school site, Adults and students/caregivers willing to participate in the study

2. For Cue Centered Therapy:

   1. Youth aged 11-17 with exposure to at least one Diagnostic Statistical Manual (DSM) 5-defined traumatic event and meeting threshold criteria for posttraumatic symptoms per the University of California Los Angeles (UCLA) PTSD scale.
   2. Willingness to participate in therapy
   3. Caregiver willing to participate in therapy
   4. Perpetrator of the traumatic event is not living in the home with the child

Exclusion Criteria

1. For the general study and for Cue Centered Therapy:

2. Students doing current trauma-focused interventions with a mental health professional

3. Low cognitive functioning (IQ less than 70)

4. Substance dependence as defined by DSM criteria

5. Autism/Schizophrenia

6. Clinically significant medical illness

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
iSWAB-DNA	iSWAB-DNA	Students that give prior consent to participating in DNA buccal swabs and the mindfulness curriculum are randomly selected to give buccal swabs prior to and after the mindfulness curriculum intervention. A subset of those students that qualify for CCT will give another buccal swab after CCT completion. DNA will be sent to Dr. Urban's lab for analysis of genetic resilience markers.
Mindfulness Curriculum	Start with the Heart Students	Participants will undergo a mindfulness curriculum in the classroom for 6-8 weeks and complete surveys before the start and after completion.
Teachers	Start with the Heart Teachers	Participants will be trained in the mindfulness curriculum and implement it in the classroom for 6-8 weeks. They will complete surveys before training and after implementation.
Counselors	Cue Centered Therapy Counselors	Participants will be trained in Cue-Centered Therapy and implement the treatment with student clients for 15-18 weeks. They will complete surveys before training and after 3 months after the start of implementation.
iSWAB-DNA	Start with the Heart Students	Students that give prior consent to participating in DNA buccal swabs and the mindfulness curriculum are randomly selected to give buccal swabs prior to and after the mindfulness curriculum intervention. A subset of those students that qualify for CCT will give another buccal swab after CCT completion. DNA will be sent to Dr. Urban's lab for analysis of genetic resilience markers.
iSWAB-DNA	Cue Centered Therapy Students	Students that give prior consent to participating in DNA buccal swabs and the mindfulness curriculum are randomly selected to give buccal swabs prior to and after the mindfulness curriculum intervention. A subset of those students that qualify for CCT will give another buccal swab after CCT completion. DNA will be sent to Dr. Urban's lab for analysis of genetic resilience markers.
CCT	Cue Centered Therapy Students	Participants that report PTSD symptomatology during the mindfulness curriculum surveys will be eligible to participate in Cue-Centered Therapy treatment for 15-18 weeks. They will complete surveys before and after treatment.

Primary Outcome Measures

Name	Time	Method
Mean Change from Baseline in Work Self-Efficacy Score	Teachers: Baseline, week 8; Counselors: Baseline, week 23	Work Self-Efficacy is assessed on a 5- point Likert scale. Score range 1 to 5 (1=Not well at all, 5=Very Well). The total score is summed. Changes in scores will be assessed between all time points.
Mean Change from Baseline in Resilience Score	Three time points: Baseline, week 8, week 23	Resilience is assessed using the Child/Youth and Adult Resilience Measure on a 5- point Likert scale. Score range 1 to 5 (1=Not at all, 5=A lot). The total score is summed. Changes in scores will be assessed between all time points.
Mean Change from Baseline in Somatic Symptoms Score	Three time points: Baseline, week 8, week 23	Somatic symptoms are assessed using the PHQ-15 on a 3- point Likert scale. Score range 0 to 2 (0=Not bothered at all, 2=Bothered a lot). Total score is summed. Changes in scores will be assessed between all time points.
Mean Change from Baseline in Anxiety Score	Three time points: Baseline, week 8, week 23	Generalized Anxiety Disorder (GAD) symptoms are assessed using the GAD-7 on a 4- point Likert scale. Score range 0 to 3 (0=Not at all, 3=Nearly every day). Total score is summed. Changes in scores will be assessed between all time points.
Mean Change from Baseline in Depression Score	Three time points: Baseline, week 8, week 23	Depression is assessed using the Patient Health Questionnaire (PHQ)-8 on a 4- point Likert scale. Score range 0 to 3 (0=Not at all, 3=Nearly every day). Total score is summed. Changes in scores will be assessed between all time points.
Changes in Methylation Pattern of Genes	Three time points: Baseline, week 8, week 23	Using DNA methylation to analyze DNA samples from buccal swabs to investigate genetic markers of resilience. Genetic markers to be analyzed include: CTNNB1, ITGB8, CSRP2, WTAP, TSC22D1, HNRNPH1, NTRK2, DCX, CDK14, PTNN, SLC1A3, IGFBP2, ERBB4. Changes in genetic expressions will be assessed between all time points.

Secondary Outcome Measures

Name	Time	Method
Mean Change from Baseline in Sleep Quality Score	Three time points: Baseline, week 8, week 23	Sleep quality is assessed using the Brief-Pittsburgh Sleep Quality Index. Questions are open answer (i.e. When have you usually gone to bed at night? How many hours of actual sleep did you get at night?). Total score is calculated by summing subscores of sleep duration, latency, day dysfunction, sleep efficiency, sleep quality, and meds. Changes in scores will be assessed between all time points.
Mean Change from Baseline in Family Functioning Score	Three time points: Baseline, week 8, week 23	Family functioning are assessed using the Family Assessment Device on a 4- point Likert scale. Score range 1 to 4 (1=Strongly Agree, 4=Strongly Disagree). Unhealthy responses are reverse-scored and each subscale is averaged. Only the General Functioning subscale will be used for the study. Changes in scores will be assessed between all time points.

Trial Locations

Locations (2)

Stanford University; 🇺🇸 Palo Alto, California, United States

Centros Sor Isolina Ferre; 🇵🇷 San Juan, Puerto Rico