Actively Recruiting
Enhancing Mother-Child Ties and Psychosocial Wellness Through Arts Among Children With Intellectual Disability and Their Mothers
Led by The University of Hong Kong · Updated on 2025-05-13
154
Participants Needed
1
Research Sites
181 weeks
Total Duration
On this page
Sponsors
T
The University of Hong Kong
Lead Sponsor
H
Hong Chi Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
The caregiving of children with intellectual disability (ID) is intensive and challenging. Caregivers, particularly mothers, are left in a vulnerable and stressful condition. Children with ID may experience difficulties in expressing emotions and may have behavioral or emotional problems. These difficulties impose extra challenges for the parents to understand and interact with their children with ID. Existing intervention programs for families having children with ID primarily focus on problem-and-emotion-focused measures. While strategies focusing on improving parent-child relationships, mother-child communication, and wellness of the dyads are limited. Expressive arts-based intervention (EXAT) adopts multiple art modalities for achieving therapeutic goals. It can bypass verbal expression and complicated cognitive processing during interactions, and it is also safe, engaging, enjoyable, and empowering. While existing evidence supports the use of arts-based intervention on children and their parents, there is a limited understanding of the application of dyadic EXAT on the mother-child relationship and their wellness. The main objective of this study is to evaluate the effectiveness of the dyadic Expressive Arts-based Intervention (EXAT) on the psychosocial well-being of mother-child dyads. Primary outcomes include parent-child relationship, parenting stress, and caregiver burnout; secondary outcomes include mother's affect and quality of life; child's mood, emotional expression, behavioral and emotional problems. This study adopts a mixed-methods design with quantitative, qualitative, and art-based assessment methods. This study is a randomized controlled trial, running for 3 years for evaluating the effectiveness of the dyadic Expressive Arts-based Intervention (EXAT). 154 Chinese mother-child dyads will be randomized into (i) a dyadic EXAT group or (ii) a treatment-as-usual waitlist control group. Quantitative analysis will be adopted to investigate the effectiveness of the dyadic intervention on the psychosocial outcomes of children with ID and their caregiving mothers. The qualitative component will consist of longitudinal in-depth interviews with mothers to understand the experiences, perceived changes, and factors that facilitate the process. Art-based assessment will also be used to understand the changes in the emotional expression of children with ID. Data collected will be triangulated to provide an integrative evaluation of the effectiveness of the intervention.
CONDITIONS
Official Title
Enhancing Mother-Child Ties and Psychosocial Wellness Through Arts Among Children With Intellectual Disability and Their Mothers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The child is 6-12 years old (primary school student)
- The child is diagnosed with mild to moderate intellectual disability with IQ score between 35 and 69
- The child is judged capable of responding to assessments and participating in group activities by health or school professionals
- The mother-child dyad is willing and able to give consent for participation
You will not qualify if you...
- The mother-child dyad is currently participating in any other behavioral or pharmacological trial
- Either the mother or child has contraindications or severe comorbidities that may impair full participation, such as severe physical disabilities
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Centre on Behavioral Health HKU
Hong Kong, Hong Kong
Actively Recruiting
Research Team
R
Rainbow Ho
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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