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Clinical Trials in Taiwan / NCT07118293
Enrolling by invitation Not applicable

Developing and Examine the Efficacy of the Family-Centered Multi-Sensory Environment Intervention on Parent's Empowerment and Children's Engagement (MSE-PEACE) in Children With Developmental Disabilities and Their Parents: A Mixed Methods Study

NCT07118293 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2026-04-13

Condition(s) studied

Developmental Disability

Investigational drug(s) / intervention(s)

MSE-PEACE

MSE-PEACE: The MSE-PEACE (Multi-Sensory Environment-Parent Empowerment and Child Engagement) intervention is a family-centered, therapist-guided sensory integration program specifically developed for children with developmental disabilities and their caregivers. Unlike traditional child-only sensory therapies, this intervention actively involves parents in all stages-assessment, goal setting, activity participation, and follow-up. Each participant dyad (parent and child) attends 10 biweekly sessions (60 minutes each) in a structured sensory therapy space equipped with adjustable lighting, tactile materials, auditory inputs, and other multisensory tools. The intervention is tailored to each child's sensory processing profile and emotional regulation needs, while promoting parent-child co-regulation, bonding, and collaborative engagement. Occupational therapists facilitate the sessions using individualized strategies to support child-led participation and empower parents with real-time coaching,

Study summary

The goal of this clinical trial is to learn whether a family-centered multi-sensory environment (MSE-PEACE) can help children with developmental disabilities and support their parents. The main questions it aims to answer are:

Can the MSE-PEACE program improve children's participation and emotional self-regulation? Does it help parents feel more confident and empowered in their caregiving role?

Participants will include children ages 3 to 12 years and their parents. All children have been diagnosed with a developmental disability such as autism, ADHD, or cerebral palsy. Participants will:

Join 10 multi-sensory sessions, held every 2 weeks, each lasting about 60 minutes Complete questionnaires and interviews before and after the sessions Receive support and suggestions for using sensory-based activities at home

This study will collect both survey and interview data to understand how the program affects children's daily functioning and how it supports parents' confidence and well-being.

Eligibility

Sex
ALL
Min age
3 Years
Max age
12 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Children aged 3 to 12 years * Diagnosed with a developmental disability (e.g., autism spectrum disorder, attention-deficit/hyperactivity disorder, cerebral palsy, global developmental delay) * Able to attend 10 biweekly intervention sessions in person with a caregiver * Caregiver is the primary caregiver and agrees to actively participate in all sessions * Caregiver is able to complete written questionnaires in Chinese * Caregiver provides informed consent Exclusion Criteria: * Child has significant physical or behavioral challenges that prevent safe participation in a multi-sensory therapy setting (e.g., uncontrollable aggression, high seizure risk) * Caregiver has cognitive or psychiatric conditions that significantly limit the ability to participate in shared sessions or complete questionnaires

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Occupational Therapy, National Cheng Kung University Tainan Taiwan

More National Cheng Kung University trials in Taiwan

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 NCT07118293 on ClinicalTrials.gov ↗ ← All trials in Taiwan