NCT07869251

Brief Summary

Parents of children with developmental disabilities (DD) consistently report significant psychological distress, a vulnerability amplified during the COVID-19 pandemic due to intensified caregiving demands and reduced access to formal supports. Scalable e-health interventions offer a promising alternative, yet programs specifically targeting the mental wellbeing of this parent population remain limited. This study aimed to examine the impact of the 90SecondParent Wellbeing e-health intervention on psychological wellbeing, parental wellbeing, and symptoms of depression and anxiety among parents of children with developmental disabilities. A two-arm randomized controlled trial of primary caregivers of children with developmental disabilities was conducted with a wait-list control group. The intervention consisted of 36 weekly health letters (the 90SecondParent Wellbeing program) that addressed child behaviour management, support strategies, and positive psychology principles. Outcomes, including psychological wellbeing (PWBS), parental wellbeing (PWS), depression (PHQ-9), and anxiety (GAD-7), were assessed across three time points ( baseline, immediately after intervention, and 1 month post-intervention (follow-up)).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 19, 2022

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 7, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 7, 2024

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

September 28, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

October 9, 2026

Completed
Last Updated

October 9, 2026

Status Verified

October 1, 2026

Enrollment Period

2 years

First QC Date

September 28, 2026

Last Update Submit

October 6, 2026

Conditions

Keywords

Public health e-interventionParenting intervention

Outcome Measures

Primary Outcomes (1)

  • Psychological wellbeing (PWBS)

    The Psychological Wellbeing (PWBS) measure assesses six aspects of wellbeing: autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, and self-acceptance. Items are rated on a 7-point Likert-type scale ranging from 1 (Strongly agree) to 7 (Strongly disagree). Higher scores indicate greater wellbeing. The PWBS was measured at baseline, post-assessment, and follow-up.Total scores range from 18 to 126, with higher scores indicating greater psychological wellbeing.

    Baseline, Immediately after intervention (18 weeks), 1 month post-intervention

Secondary Outcomes (1)

  • Parent Wellbeing

    Baseline, Immediately after intervention (18 weeks), 1 month post-intervention

Other Outcomes (2)

  • Depressive symptoms

    Baseline, Immediately after intervention (18 weeks), 1 month post-intervention

  • Generalized Anxiety Symptoms

    Baseline, Immediately after intervention (18 weeks), 1 month post-intervention

Study Arms (2)

90SecondParent Wellbeing Intervention

EXPERIMENTAL

They received 36 weekly health letters (the 90SecondParent Wellbeing program) that addressed child behaviour management, support strategies, and positive psychology principles.

Behavioral: 90SecondParent Wellbeing

Waitlist Control Group

NO INTERVENTION

They didn't receive an intervention and only received access to the health letters after completing the follow-up assessment.

Interventions

The intervention consisted of 36 weekly health letters that addressed child behaviour management, support strategies, and positive psychology principles.

90SecondParent Wellbeing Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Parent or caregiver of a child with a developmental disability.
  • At least 18 years of age
  • Spent a minimum of 20 hours per week, for at least the past 3 months, to care for their child with developmental disabilities
  • Living in Canada
  • Able to read, write, and understand English.
  • Provided informed consent.
  • Access to a tablet, smart phone, computer, or internet

You may not qualify if:

  • Not a parent or caregiver of a child with a developmental disability.
  • Spent less than 20 hours per week for less than 3 months caring for a child with developmental disabilities
  • Didn't live in Canada
  • Not able to read, write, and understand English.
  • No access to a tablet, smart phone, computer, or internet.
  • Did not consent to the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

IWK Health Centre

Halifax, Nova Scotia, B3K6R8, Canada

Location

MeSH Terms

Conditions

Developmental Disabilities

Condition Hierarchy (Ancestors)

Neurodevelopmental DisordersMental Disorders

Study Officials

  • Patrick J McGrath, PhD

    IWK Health Centre

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 28, 2026

First Posted

October 9, 2026

Study Start

October 19, 2022

Primary Completion

October 7, 2024

Study Completion

October 7, 2024

Last Updated

October 9, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will share

Participants were asked to indicate during Informed Consent whether their de-identified data may be shared with other researchers, provided the study is approved by an ethics board and researchers agree to use the data only for the purposes described in the approved research study. De-identified data from all outcome measures will be made available to approved researchers upon request, provided individual participants have provided consent.

Shared Documents
STUDY PROTOCOL, SAP, ICF

Locations