Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
ID06086951

Pai.ACT: A Deep-learning-powered, Smartphone-delivered Acceptance and Commitment Therapy for Parents of Children With Special Needs: A Feasibility Study

Led by Chinese University of Hong Kong · Updated on 2025-01-23

60

Participants Needed

2

Research Sites

13 weeks

Total Duration

On this page

Sponsors

C

Chinese University of Hong Kong

Lead Sponsor

H

Hong Kong Christian Service

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating Pai.ACT, a smartphone-based mental health advisory system using deep learning and Acceptance and Commitment Therapy (ACT) designed for parents of children with special needs in Hong Kong. This trial aims to test the feasibility, acceptability, and potential benefits of Pai.ACT in improving mental health outcomes for these parents compared to conventional familial support. The study addresses the psychological burden parents face due to limited mental health services and prolonged waiting times for their children's rehabilitation, focusing on parents of children aged 2 to 8 years diagnosed or suspected with developmental conditions such as autism spectrum disorder and ADHD. The study involves two groups: one group will use the Pai.ACT mobile app, which offers voice-to-text conversations with an AI chatbot providing personalized ACT-based interventions, including self-help modules, dynamic exercises, and 4-6 video counseling sessions. The other group will receive usual care through familial support programs and educational materials from hospital and non-governmental organizations. The intervention period and follow-up last for three months post-intervention to observe changes in mental well-being. Participants will engage in assessments measuring parenting stress, child emotional and behavioral symptoms, anxiety, depression, psychological flexibility, and app usability at baseline, immediately after the intervention, and three months later. The study uses randomized allocation and double-blinding to compare outcomes between groups. Parents will be monitored throughout for mental health changes and intervention acceptability, with the total study duration covering these evaluation points.

CONDITIONS

Brief Title

Pai.ACT - An Artificial Intelligence Driven Chatbot Assisted ACT

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary caregivers who are Cantonese-speaking residents of Hong Kong
  • Caregivers must live with a child with special needs
  • Child must be aged 2 to 8 years
  • Child must have a diagnosis or suspected diagnosis of ASD, ADHD, or developmental delays recognized by the Child Assessment Service and documented in medical records
Not Eligible

You will not qualify if you...

  • Parents diagnosed with severe mental illnesses
  • Parents who are currently pregnant
  • Parents less than six months postpartum
  • Parents with developmental disabilities affecting comprehension
  • Parents with cognitive, language, communication, vision, or hearing impairments that affect understanding
  • Parents currently participating in other psychosocial, psychoeducational, or parenting programs

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Treatment

Duration - 3 months

Participants receive the Pai.ACT intervention via a smartphone app that delivers Acceptance and Commitment Therapy (ACT) through self-help modules, experiential exercises, and 4-6 video-based individual ACT sessions with a counseling team. The control group receives conventional familial support and educational content.

Ongoing app use with periodic video sessions; assessment visits at baseline and immediately post-intervention

Follow-up

Duration - 3 months post-intervention

Participants are monitored for continued mental well-being and psychological flexibility up to three months after completing the intervention.

1 follow-up visit

Trial Site Locations

Total: 2 locations

1

The Chinese University of Hong Kong

Hong Kong, Hong Kong

Actively Recruiting

2

The Pamela Youde Nethersole Eastern Hospital

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

Y

Yuen Yu CHONG, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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