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RecruitingNCT07749521OPTEDUpdated Nov 9, 2026

Optimizing Treatment for Depressed Parents of Children With Emotional and Behavioural Problems

An interventional study of ADAPT Treatment and Incredible Years Parenting Program (IYPP) in Depression / Major Depressive Disorder, Conduct Disorders in Children and Disruptive Behaviour in Children, sponsored by University of Toronto. Recruiting at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by University of Toronto · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 3 months later.
Updated Nov 9, 2026Enrollment updatedEligibility revisedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
210
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Standard Behavioral Parent Training (BPT) is often less effective for parents experiencing depression. As such, the Addressing Depression and Positive Parenting Techniques (ADAPT) intervention is a novel BPT tailored to address the unique emotional and cognitive needs of depressed parents to improve treatment outcomes.

The objective of this study is to determine the efficacy of ADAPT in reducing child emotional and behavioral difficulties compared to the gold-standard Incredible Years Parenting Program (IYPP).

This study is a 4-year, individually-randomized group treatment (IRGT), parallel-group trial. We aim to recruit 210 caregivers and their children (aged 6-11 years) seeking treatment for their child's emotional and behavioral difficulties from multiple mental health centres across Toronto, including but not limited to the University of Toronto, Centre for Addiction and Mental Health (CAMH), and Women's College Hospital (WCH).

Participants will be asked to complete research measures:

  • before randomization
  • post-treatment
  • 6 months after the end of treatment

Participants will be randomized to either the experimental ADAPT intervention - A 10-session virtual program (1 individual, 9 group) focused on emotion regulation, distress tolerance, and cognitive restructuring, or the control intervention: Incredible Years Parent Program (IYPP) - A 12-session gold-standard BPT delivered virtually.

02

Conditions studied

  • Depression / Major Depressive Disorder
  • Conduct Disorders in Children
  • Disruptive Behaviour in Children
  • Parenting Intervention

Keywords

  • behavioural parent training
  • depression
  • parenting skills
  • child disruptive behaviour
03

In context

Depression

8,577 studies on the registry are indexed under Depression; 1,720 are open to participants now.

This study's planned enrollment of 210 is above the median of 81 across 7,063 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

University of Toronto is the lead sponsor of 403 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

The criteria were revised on the registry on Nov 9, 2026. See what changed

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. 18 years of age or above
  2. has a child aged 6-11 years with clinically elevated emotional and behavioural disorders (Abnormal Range, 90th percentile or above) on the Total Difficulties Scale or the Conduct Problems subscale of the Strength and Difficulties Questionnaire (SDQ)
  3. parent shows clinical elevations for mild-moderate depression on the Patient Health Questionnaire-8 (PHQ-8) (>4 and \<15)
  4. capacity to tolerate a virtual group context assessed by clinical interview

Exclusion criteria

Exclusion Criteria:

  1. Parent shows active suicidal ideation, substance use disorder, or psychosis
  2. they cannot communicate in English
  3. child previously diagnosed with autism or an intellectual disability
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
210 participants (estimated)

Study arms

  • Experimental
    ADAPT Treatment

    Participants in the experimental arm will receive the novel Addressing Depression and Positiving Parenting Techniques (ADAPT) treatment. ADAPT is a targeted treatment adapted by the Co-PI based on the Parenting a Child Who Has Intense Emotions program. The treatment has modules that help parents build emotion regulation skills, distress tolerance skills, and helpful ways of thinking about their parenting. The program also contains components of standard behavioural parent training, including strategies to build family structure, routines, and predictable parenting responses to children's behavioral challenges. Additionally, ADAPT includes elements of Dialectical Behaviour Therapy (DBT), an effective intervention for the treatment of adults and youth with dysregulated emotion and behavior.

    Behavioral: ADAPT Treatment

  • Active comparator
    Incredible Years Parenting Program (IYPP)

    Participants randomized to the control arm will receive the Incredible Years Parenting Program (IYPP). IYPP is a best-practice and widely used treatment for parents of children with EBD.

    Behavioral: Incredible Years Parenting Program (IYPP)

Interventions

  • BehavioralADAPT Treatment

    ADAPT is a 10-session virtual caregiver program (one individual engagement session and nine group sessions) that was developed with clinician and parent input. The initial engagement session is an individual meeting between the group facilitator and parent to build rapport and learn about the parent's unique challenges and parenting needs. Based on a motivational interviewing framework, this session is designed to gather information, discuss readiness for treatment and goals. The questions and tools used in this session help to build a collaborative understanding of unique child and parent needs that may be addressed through ADAPT and leave the parent with the hope that ADAPT can be helpful. The 9 virtual group treatment sessions that follow include modules to help parents understand the multiple potential contributions to their child's emotional/behavioral challenges, build their own emotion regulation skills, distress tolerance skills, and more helpful ways of thinking.

  • BehavioralIncredible Years Parenting Program (IYPP)

    The 12-session manualized treatment is considered a gold-standard treatment because it has shown efficacy in large-scale randomized and controlled trials and meta-analyses. Parents are helped to shift their children's emotional and behavioral difficulties through improved parental skills and competencies with behaviour management, and a parental problem-solving approach. IYPP will be delivered virtually.

06

What researchers measure

Primary outcomes

  1. Changes in child emotional and behavioral difficulties

    Child emotional and behavioural difficulties are assessed using the Behaviour and Feelings Survey (BFS).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

Secondary outcomes

  1. Changes in parental depression

    Parental depression is assessed using the Patient Health Questionnaire (PHQ-8).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  2. Changes in parental quality of life

    Quality of life is assessed using the World Health Organization Disability Assessment 2.0 (WHODAS).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  3. Changes in broad parenting practices

    Parenting practices are assessed using the Multidimensional Assessment of Parenting (MAPS).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  4. Changes in parental stress

    Parental stress is assessed using the self-reported scores on items of the Stress subscale of the Depression, Anxiety, and Stress Scale (DASS-21).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

Other outcomes

  1. Changes in parental cognition

    Parent cognition is assessed using the Parent Cognition Scale (PCS). The PCS will be examined as a predictor of initial symptom severity and potential treatment mechanism.

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  2. Changes in parent emotion regulation

    Parent emotion regulaiton is assessed using the Affect Regulation Checklist (ARC). The PCS will be examined as a predictor of initial symptom severity and potential treatment mechanism.

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  3. Changes in real-time parent-reported child emotional and behavioral difficulties

    Real-time parent-reported child emotional and behavioral difficulties will be assessed via ecological momentary assessment (EMA) at pre- and post-treatment, capturing momentary ratings of child symptoms.

    Time frame: Baseline (pre-randomization) and post-treatment (12-weeks post-randomization)

  4. Changes in the implementation of parenting skills

    Implementation of parenting skills is assessed using the Parenting Skill Use Diary (PSUD).

    Time frame: Baseline (pre-randomization) and post-treatment (12-weeks post-randomization).

  5. Changes in child depressive symptoms

    Child depressive symptoms will be assessed using the child-reported Short Mood and Feelings Questionnaire (SMFQ).

    Time frame: Baseline (pre-randomization) and post-treatment (12-weeks post-randomization).

  6. Changes in child irritability

    Child irritability will be assessed using the parent-reported Affective Reactivity Index (ARI).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  7. Changes in child perceptions of parenting behaviour

    Child perceptions of parenting behaviour will be assessed using the Children's Report of Parenting Behavior Inventory (CRPBI).

    Time frame: Baseline (pre-randomization) and post-treatment (12-weeks post-randomization)

  8. Changes in parental competence need satisfaction and frustration

    Parental competence need satisfaction and frustration will be assessed using the relevant subscales of the Basic Psychological Need Satisfaction and Frustration Scale (BPNSFS).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

  9. Changes in child callous-unemotional traits

    Child callous-unemotional traits will be assessed using the Inventory of Callous-Unemotional Traits (ICU).

    Time frame: Baseline (pre-randomization), post-treatment (12 weeks post-randomization), and 6-month follow-up

  10. Changes in child self-reported emotion-regulation

    Child self-reported emotion-regulation will be assessed using the Children's Emotion Management Scales (CEMS).

    Time frame: Baseline (pre-randomization) and post-treatment (12 weeks post-randomization)

  11. Changes in parental self-efficacy

    Parental self-efficacy is assessed using the Parenting Sense of Competence Scale (PSOC).

    Time frame: Baseline (pre-randomization), post-treatment (12-weeks post-randomization), and 6-month follow-up

07

Study locations

1 of 1 sites recruiting
  • Ontario Institute for Studies in Education (OISE)
    Toronto, Ontario, Canada
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — De-identified study data may be shared with other reseachers upon request at the disrection of the PI.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Enrollment
180→210
Nov 9, 2026
Eligibility
1 inclusion criterion edited
What changed in the criteria
Inclusion criteria
  • Editedhas a child aged 6-11 years with clinically elevated emotional and behavioural disorders (Abnormal Range, 93rd90th percentile or above) on the Total Difficulties Scale or the Conduct Problems subscale of the Strength and Difficulties Questionnaire (SDQ)
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    Enrollment 180→210
    Eligibility 1 inclusion criterion edited
    What changed in the criteria
    Inclusion criteria
    • Editedhas a child aged 6-11 years with clinically elevated emotional and behavioural disorders (Abnormal Range, 93rd90th percentile or above) on the Total Difficulties Scale or the Conduct Problems subscale of the Strength and Difficulties Questionnaire (SDQ)
    + 3 other changes: date precision, description and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07749521
Collaborators
Centre for Addiction and Mental Health, Women's College Hospital
Responsible party
Brendan Andrade (Associate Professor, University of Toronto) — Principal investigator
First posted
Aug 6, 2026
Start date
Aug 1, 2026
Primary completion
Aug 2030 (estimated)
Completion
Aug 2030 (estimated)
Last update
Nov 9, 2026

Study contacts

Brendan Andrade, PhD
Contact
brendan.andrade@utoronto.ca
416-946-5905

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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