Strongest FamiliesTM Neurodevelopmental

NCT03835689 | Completed

• 1 other identifier: REB#1023970
• Study Type: interventional
• Target: 454
• Locations: 1 country
• Sites: 1

Brief Summary

Children and adolescents with neurodevelopmental conditions are 3 to 5 times more likely than their peers to have other mental disorders such as anxiety, depression and disruptive behaviour. Furthermore, these conditions are less likely to be recognized, diagnosed and treated than for typically developing children. Parent training is a well-established approach to help parents change their behaviour and communication with their children with the goal of improving child behaviours. Parent-focused programs that are designed for typically developing children have shown mixed results for children with neurodevelopmental conditions and parents have reported significant challenges in accessing traditional health services due to barriers to care. There is an urgent need to explore how effective distance-delivered parenting programs can be implemented in real-world settings and how they should be adapted to meet the needs of families with children with neurodevelopmental conditions. The goal of this research project is to develop and test the effectiveness of two versions (group coaching \& self-managed) of an online parenting program for managing challenging behaviours in children with neurodevelopmental disabilities. The Strongest Families Neurodevelopmental program is based on the well-established Strongest Families Parenting program for typically developing children with challenging behaviours, adapted with substantial involvement from a pan-Canadian Parent Advisory Committee. The program consists of 11 skill-based sessions with demonstration videos, audio clips, exercises, a resource webpage and a Parent-to-Parent online group (a closed Facebook group).

Conditions

Neurodevelopmental Disorders; Behavior Disorders

Keywords

Behavioural intervention; E-health intervention; Parenting intervention

Outcome Measures

Primary Outcomes (2)

• Change from baseline parenting self-efficacy at 5 month post-randomization

  Statistically significant improvement in parent report of self-efficacy from baseline to 5 month follow up for both intervention groups compared to control, as measured by the total score on the Self-Efficacy subscale of the Child Adjustment and Parent Efficacy Scale - Developmental Disability (CAPES-DD) questionnaire. The CAPES-DD assesses emotional and behavioural problems in children with developmental disabilities (age 2 - 16 years) and their parents' self-efficacy to manage specific problematic behaviours. For each of 16 problem child behaviours, respondents are asked to rate their confidence in their ability to successfully manage the behaviour. Ratings range on a scale from 1 ('certain I can't manage it') to 10 ('certain I can manage it'). Total scores range from 16 - 160 with higher scores indicating greater levels of parent self-efficacy.

  Baseline and 5 month post-randomization

• Change from baseline child's emotion regulation at 5 month post-randomization

  Statistically significant improvement in emotion regulation from baseline to 5 months for both intervention groups compared to control, as measured by the total score of the Emotion Regulation Checklist (ERC). The 24-item scale consists of two subscales: Lability/Negativity characterized by inflexibility, mood swings and dysregulated negative affect (e.g., "is prone to angry outbursts/tantrums easily"), and Emotion Regulation representing appropriate affect, empathy and awareness of one's emotions (e.g., "responds positively to neutral or friendly approaches by peers'). Parents are asked to report, on a 4 point Likert-type scale ranging from Never to Almost Always, how much each statement applies to their child. An overall emotional regulation score is calculated by reverse scoring the Emotion Regulation items and summing all questionnaire items; a higher score indicating more dysregulation. We will use total scores which range from 23 - 92 (item 12 is not used in the calculation).

  Baseline and 5 month post-randomization

Secondary Outcomes (5)

• Change from baseline parenting self-efficacy at 10 month post-randomization

  Baseline and 10 month post-randomization

• Change from baseline child's emotion regulation at 10 month post-randomization

  Baseline and 10 month post-randomization

• Reduced children's externalizing behaviours

  Baseline, 5 and 10 month post-randomization

• Improved parental well-being

  Baseline, 5 and 10 month post-randomization

• Incremental Cost-Effectiveness Ratio (ICER) - Child

  Baseline, 5 and 10 month post-randomization

Study Arms (3)

Strongest Families Program Self-Managed (no coaching)

EXPERIMENTAL

They will receive Strongest Families intervention immediately as well as the usual care services available for the 10 month study period.

Behavioral: Strongest Families Intervention (formerly Family Help)

Strongest Families Program with Group Telephone Coaching

EXPERIMENTAL

They will receive Strongest Families intervention immediately as well as the usual care services available for the 10 month study period.

Behavioral: Strongest Families Intervention (formerly Family Help)

Information Resource Website

NO INTERVENTION

They will not receive Strongest Families Intervention during the 10 month study phase, but will receive the usual care services and access to an Information Resource Website.

Interventions

Strongest Families Intervention (formerly Family Help) BEHAVIORAL

Distance HEALTH education intervention focused on skill learning for parents

Also known as: Formerly the Family Help Program

Strongest Families Program Self-Managed (no coaching); Strongest Families Program with Group Telephone Coaching

Eligibility Criteria

• Age: 3 Years - 14 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17)

SCREENING: Parents/caregivers must meet all of the following criteria to be eligible to proceed to Consent: 1. Have a child between 3-14 years of age with a diagnosis of a neurodevelopmental disorder (i.e. Autism Spectrum Disorder, Cerebral Palsy, Epilepsy, Global Developmental Delay, Down Syndrome, Fetal Alcohol Spectrum Disorder (FASD), severe learning disability or any other diagnosis that influences how their child gets around, communicates their ideas, processes what they hear, or remembers things as reported by parents/caregivers). 2. The child has been experiencing behavioural problems that interfere with the activities of daily living (as defined by the caregiver) for at least 6 months prior to study screening. 3. Have been the primary caregiver for a minimum of 6 months prior to entry into the study. 4. Have a reasonable expectation of being be the primary caregiver for at least 10 months after study enrolment. 5. Read, write, and understand English. 6. Have access to a telephone. 7. Have regular access to a tablet, smartphone or computer connected to high speed Internet. 8. Live in Canada. 9. Commit to the requirements of taking part in the study (e.g. available to attend weekly coaching calls, having a Facebook account to access Parent-to-Parent support group) Any of the following criteria will exclude individuals from proceeding to Consent: 1. Child is NOT able to understand everyday language and instructions or communicate needs as reported by parent/caregiver. 2. Parent or child has ongoing struggles with symptoms of psychosis, schizophrenia, bipolar disorder or major depression (i.e. the symptoms are not well managed). 3. Child is at imminent risk of serious harm to self or others (i.e. requiring hospitalization or medical attention). 4. Child regularly engages in moderate to severe self-injurious behaviours, as reported by the parent. 5. Child has attempted suicide in the past 6 months. 6. Parent has previously taken part in a Strongest Families Parenting Program. 7. Parent has taken part in Triple P, COPE, Incredible Years or another parent training program within 6 months prior to starting the study. BASELINE ASSESSMENT: 1. Meet minimum score of 16 (for ages 2 - 4 years) or 17 (for ages 4-17) on the Total Difficulties Score of the Strengths and Difficulties Questionnaire. 2. Meet a minimum level of child's cognitive functioning as determined by the question\* below. Parents must endorse 1, 2 or 3 on the following question: Compared with children of the same age, does your child have difficulty learning things? Would you say your child has: no difficulty, some difficulty, a lot of difficulty or cannot do at all? No difficulty........................ 1 Some difficulty....................2 A lot of difficulty..................3 Cannot do at .....................4

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• IWK Health Centre: lead
• Canadian Institutes of Health Research (CIHR): collaborator
• McGill University: collaborator
• University of Alberta: collaborator
• Child-Bright Network: collaborator

Study Sites (1)

IWK Health Centre

Halifax, Nova Scotia, B3K6R8, Canada

Location

MeSH Terms

Conditions

Neurodevelopmental Disorders; Mental Disorders

Study Officials

• Patrick J McGrath, PhD

  IWK Health Centre

  PRINCIPAL INVESTIGATOR

• Lucyna Lach, PhD

  McGill University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Masking Details: Statistician conducting analysis will be blinded to group assignment
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal investigator

Study Record Dates

• First Submitted: February 4, 2019
• First Posted: February 8, 2019
• Study Start: April 8, 2019
• Primary Completion: August 29, 2022
• Study Completion: August 29, 2022
• Last Updated: October 4, 2024

Record last verified: 2022-03

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP, ICF

Locations

CA (1)