- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07047378
- Original Trial
ACT-Based Training for Parental Burnout and Child Well-being
Acceptance and Commitment Therapy-Based Training Programme for Reducing Parental Burnout and Improving Emotional and Behavioural Issues in Children: A Pilot Randomised Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Parental burnout is becoming more widely recognized as a serious social issue. It is particularly prevalent among high-stress families like those impacted by child maltreatment or domestic violence. According to prior research, psychological flexibility-a core component of Acceptance and Commitment Therapy (ACT)-is crucial for promoting healthy parent-child relationships and adaptive parenting practices. However, there is still a dearth of empirical evidence supporting ACT-based interventions for reducing parental burnout and improving child adjustment.
The purpose of this study is to investigate how ACT interventions differ in their impact on parents and children in Hong Kong. The specific aims are to evaluate the effectiveness of an ACT-based training program in lowering parental burnout and investigate its influence on children's emotional and behavioral adjustment.
Parents will participate in an ACT-based parenting training program designed to increase psychological flexibility in the ACT intervention group. Aiming at improving psychological flexibility and reducing parental burnout, the training program incorporates mindfulness, values-based parenting, and cognitive defusion strategies. It provides parents with the resources they require to manage stress, regulate emotions, and promote parent-child relationships, which benefits both themselves and their children.
To foster emotional regulation and resilience, children aged 6-11 will also participate in a group-based, child-focused ACT Program designed for their developmental needs. This program incorporates experiential learning exercises, mindfulness activities, and storytelling using picture books to facilitate participation and engagement. These child-focused components seek to reinforce the skills parents have learned while directly supporting child adjustment.
This study aims to examine the feasibility, acceptability, and potential efficacy of a group-based Acceptance and Commitment Therapy (ACT) intervention targeting. The intervention is designed to improve parental psychological flexibility and parenting behaviour, enhance parent- child relationships, and child-related outcomes within a separate sample of parents and children over the 3- month post-intervention. The study will be conducted in collaboration with Harmony Home Limited, leveraging the expertise of paraprofessionals trained in ACT.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Yuen Yu Chong, PhD
- Phone Number: (852) 3943 0665
- Email: conniechong@cuhk.edu.hk
Study Contact Backup
- Name: Choi Hung TANG
- Phone Number: (852) 3943 5016
- Email: choihungchtang227@cuhk.edu.hk
Study Locations
-
-
-
Kwun Tong, Hong Kong
- Recruiting
- Harmony House Limited
-
Contact:
- Choi Hung TANG
- Phone Number: (852) 3943 5016
- Email: choihungchtang227@cuhk.edu.hk
-
Sha Tin, Hong Kong
- Recruiting
- Chinese University of Hong Kong
-
Contact:
- Choi Hung TANG
- Phone Number: (852) 3943 5016
- Email: choihungchtang227@cuhk.edu.hk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
For the Parent ACT Group:
- Cantonese-speaking Hong Kong residents between the ages of 19 and 65 years.
- Primary caregivers of a child aged 3 to 11 years.
- Have been identified by school social workers as being at risk of domestic violence or experiencing emotional distress.
For the Child ACT Group:
- Cantonese-speaking Hong Kong residents between the ages of 3 and 11 years.
- Have been identified by school social workers as being at risk of domestic violence or experiencing emotional distress.
For both groups (Shared inclusion criteria):
- Participants must have sufficient Cantonese language proficiency to understand and communicate during the intervention.
- Both parents and children must provide informed consent to participate in the study and all related assessments.
Exclusion Criteria:
For the Parent ACT Group:
- Parents diagnosed with severe mental illnesses.
- Parents with a developmental disability that interferes with their ability to comprehend the program's content.
- Parents with cognitive, language, communication, visual, or hearing impairments or disorders that could impede their understanding of the intervention content; or
- Parents currently participate in other psychosocial, psychoeducational, or parenting interventions.
- Parents with active substance abuse issues that may interfere with their ability to participate in or benefit from the program.
- Parents whose children have been diagnosed with psychological or medical conditions.
For the Child ACT Group:
1. Children who have been diagnosed with psychological or medical conditions.
For both groups (Shared Exclusion criteria):
- Families who are unable or unwilling to commit to attending the six-week sessions or completing follow-up assessments.
- Families who lack access to transportation or other necessary resources to attend the intervention sessions
- Parents and children who cannot understand or communicate in the language used in the intervention and assessments (i.e., Cantonese and Chinese).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ACT Intervention Group
Both ACT Intervention and the Control Group will receive standard services originally provided by Harmony House.
For parents allocated to this experimental group, 6 sessions of the ACT-based parenting program, one weekly session, 90 minutes per session.
For children allocated to this experimental group, 6 sessions of the child-focused ACT programme, one weekly session, 90 minutes per session.
|
For Parent ACT Group, parents will participate in a six-week, group-based ACT program integrated with behavioral parenting training based on positive parenting principles. Each session lasts two hours and includes 65 minutes of ACT-based activities (e.g., experiential exercises, guided imagery, mindfulness, values clarification, metaphors) and 25 minutes of parenting education and/or behavioral skills training. For Children ACT Group, children (aged 6-11) will also receive a child-focused ACT intervention to help them manage emotional challenges. Each session lasts two hours and includes 65 minutes of ACT-based activities (e.g., experiential exercises, guided imagery, mindfulness, values clarification, metaphors) and 25 minutes of behavioral skills training. |
|
Other: Control Group
Participants allocated to the Control Group will not receive the ACT intervention during the initial 3-month study period but will be offered the intervention afterward as part of a waitlist control design.
|
Participants allocated to the Control Group will not receive the ACT intervention but will continue to receive the standard services originally provided by Harmony House. These services constitute usual care and include initial assessments, individual counselling, group counselling, the provision of community resource information, and referrals. Control group participants will receive these supports as usual. This study will not alter their existing service arrangements in any way, nor will it add to or reduce the support they receive. Aside from not participating in the ACT program, the control group's experience will be identical to that of clients receiving regular services. After the intervention group completes the program, the control group will be offered the same course content (i.e., a waitlist intervention arrangement). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Burnout
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
The Parental Burnout Assessment (PBA, 23-item, 7-point Likert scale) will be employed to evaluate the level of parental burnout.
The Chinese version of PBA has reported good internal consistency (Cronbach's α = >.8),
adequate construct validity (.66~.79), and strong convergent validity in Chinese parents.
|
Change from baseline assessment to immediate and 3 months post-intervention
|
|
Children's emotional and behavioral adjustment
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
The Strengths and Difficulties Questionnaire (SDQ, 25-item, 3-point Likert scale) will be used to assess children's emotional and behavioral adjustment.
The Chinese version of SDQ demonstrates satisfactory internal consistency (Cronbach's α = .45-.90) and good test-retest reliability (coefficients = 0.8 to 0.85).
|
Change from baseline assessment to immediate and 3 months post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Psychological flexibility
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
Parental Psychological Flexibility Questionnaire (PPFQ, 16-item, 7-point Likert scale) will be employed to measure parents' psychological flexibility.
The PPFQ measures psychological flexibility using three subscales: cognitive defusion, committed action, and acceptance.
The total and each subscale scores of the Chinese version of PPFQ have demonstrated substantial discriminant and criterion validity and internal consistency (Cronbach's α = .77-.86), and test-retest reliability coefficients ranging from 0.55 to 0.75.
|
Change from baseline assessment to immediate and 3 months post-intervention
|
|
Children's psychological flexibility
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
Child and Adolescent Mindfulness Measure (CAMM, 10-item, 5-point Likert scale) will be used to assess children's psychological flexibility through children's self-reports.
Grounded in Acceptance and Commitment Therapy (ACT), it measures present-moment awareness and non-judgmental acceptance of thoughts and feelings.
The Chinese version of CAMM demonstrates good internal consistency (Cronbach's α = .826)
and strong construct validity and acceptable criterion-related validity among Chinese primary school students.
|
Change from baseline assessment to immediate and 3 months post-intervention
|
|
Adaptive parenting behaviors
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
Interpersonal Mindfulness in Parenting Scale (IM-P, 31-item, 5-point Likert scale), a parent self-report measure, will be employed to measure adaptive parenting behaviors.
The IM-P assesses five dimensions: Listening with Full Attention, Emotional Awareness of Self and Child, Self-Regulation in Parenting, Non-Judgmental Acceptance of Self and Child, and Compassion for Self and Child.
The Chinese version of the IM-P was found to have adequate internal consistency (Cronbach's α = 0.85) and has been demonstrated to be a valid measure among Chinese populations.
|
Change from baseline assessment to immediate and 3 months post-intervention
|
|
Parent-Child Relationship Quality
Time Frame: Change from baseline assessment to immediate and 3 months post-intervention
|
Child-Parent Relationship Scale-Short Form (CPRS-SF, 15-item, 5-point Likert scale), a parent self-report measure, will be used to assess the quality of the parent- child relationship.
The Chinese version of CPRS-SF assesses child-parent relationships across two subscales: conflict and closeness.
The internal consistency of the subscales is typically reported as being in the range of 0.70 to 0.90, indicating good reliability.
|
Change from baseline assessment to immediate and 3 months post-intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NTEC-2025-184
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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