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Clinical Trials in Canada / NCT07685990
Starting soon Not applicable

Trauma Therapy for Weight-Based Bullying in Children

NCT07685990 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-07-06

Condition(s) studied

Pediatric ObesityWeight-based BullyingPsychological Trauma

Investigational drug(s) / intervention(s)

Trauma Therapy for Weight-Based Bullying Informed by TF-CBT

Trauma Therapy for Weight-Based Bullying Informed by TF-CBT: This intervention is a trauma therapy program for children and adolescents experiencing distress related to weight-based bullying. The intervention is informed by the core principles and components of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) and is adapted to address bullying-related trauma, body image concerns, emotional distress, maladaptive eating behaviours, and weight-related stigma. The intervention includes psychoeducation, emotional regulation and coping skills, cognitive coping strategies, trauma narrative development and processing, body image and stigma-related cognitive restructuring, caregiver support strategies, and safety planning as clinically indicated. Treatment is developmentally tailored and delivered virtually within the HEAL Program at Children's Hospital, London Health Sciences Centre. Participants will complete approximately 12 weekly therapy sessions delivered by a trained MSW/RSW clinician.

Study summary

The goal of this feasibility study is to learn whether a trauma therapy intervention for children and adolescents who have experienced weight-based bullying can be successfully delivered within a pediatric weight management program. The intervention is informed by Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) principles and is designed to address trauma-related distress, body image concerns, emotional difficulties, and eating-related challenges associated with weight-based bullying. The main questions this study aims to answer are:

* Can this trauma therapy intervention be feasibly implemented within the HEAL Program at Children's Hospital, London Health Sciences Centre?
* Is the intervention acceptable and helpful for participating children, adolescents, and caregivers?
* Are exploratory changes observed in trauma symptoms, emotional well-being, self-esteem, eating-related concerns, and weight-related distress following participation in the intervention?

Participants will:

* Participate in approximately 12 weekly virtual therapy sessions, with flexibility for additional sessions if clinically needed
* Complete questionnaires before and after treatment related to emotional well-being, trauma symptoms, eating-related concerns, and body image
* Participate in selected caregiver-supported sessions during treatment
* Optionally complete a brief feedback interview about their experience in the program after treatment is completed

The study will also examine recruitment, attendance, treatment completion, and participant satisfaction to help determine whether this intervention can be implemented in routine clinical care settings.

Eligibility

Sex
ALL
Min age
10 Years
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: * Children and adolescents aged 10-17 years enrolled in the HEAL Program at Children's Hospital, London Health Sciences Centre * Self-reported experiences of weight-based bullying or weight-related teasing associated with emotional distress * Clinically appropriate for outpatient trauma therapy participation as determined by the study team * Ability to participate in virtual therapy sessions in English * Willingness of both participant and caregiver to participate in study procedures and intervention components * Ability of the participant and caregiver to provide informed assent/consent Exclusion Criteria: * Acute psychiatric risk requiring a higher level of care (e.g.: active suicidal ideation with intent or plan, recent suicide attempt requiring crisis intervention, psychosis or loss of reality testing, severe psychiatric instability); * Severe eating disorder requiring specialized or intensive treatment; * Uncontrolled or medically unstable conditions requiring urgent or intensive intervention; * Developmental or cognitive conditions that significantly impair participation in TF-CBT; * Concurrent participation in other trauma-focused psychotherapy or interventions targeting trauma symptoms; * Pregnancy; * Lack of caregiver availability for treatment participation. * Not able to do virtual sessions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
London Health Sciences Centre London Ontario

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07685990 on ClinicalTrials.gov ↗ ← All trials in Canada