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Child AbuseNCT07047378

ACT-Based Training for Parental Burnout and Child Well-being

A study testing ACT Intervention Group in people with Child Abuse and Parental Burnout, run by Chinese University of Hong Kong at 2 sites in Hong Kong.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of the proposed randomized controlled trial is to evaluate the feasibility, acceptability, and potential effectiveness of Acceptance and Commitment Therapy (ACT) in reducing parental burnout and improving children's emotional and behavioral adjustment in families in Hong Kong over 3 months after the… Read more about this study

Who is it for?
Ages 3 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Child Abuse, Parental Burnout
What is being tested?
ACT Intervention Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
120 participants
Where
2 sitesHong Kong
Study dates
22 Apr 2025to 30 Apr 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • 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.
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  • 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.

Who cannot join

  • 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.
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  • 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).

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Hong Kong2 sites, 2 recruiting
  • Harmony House Limited

    Kwun Tong

    Choi Hung TANG, (852) 3943 5016, choihungchtang227@cuhk.edu.hk

    Recruiting
  • Chinese University of Hong Kong

    Shatin

    Choi Hung TANG, (852) 3943 5016, choihungchtang227@cuhk.edu.hk

    Recruiting

Other trials in Hong Kong

About this study

Official title: Acceptance and Commitment Therapy-Based Training Programme for Reducing Parental Burnout and Improving Emotional and Behavioural Issues in Children: A Pilot Randomised Controlled Trial

The purpose of the proposed randomized controlled trial is to evaluate the feasibility, acceptability, and potential effectiveness of Acceptance and Commitment Therapy (ACT) in reducing parental burnout and improving children's emotional and behavioral adjustment in families in Hong Kong over 3 months after the intervention. The findings will provide valuable and scientific insights to inform better parenting interventions and child protection policies.

Read the 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.

Being tested
ACT Intervention Group, control group
Keywords
Child maltreatment, Acceptance and Commitment Therapy (ACT), Hong Kong, Parental burnout, Psychological flexibility, Feasibility, Acceptability, Child adjustment, Child emotion, Emotional development

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ACT Intervention GroupBehavioural

    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.

  • control groupOther

    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).

Study groups in NCT07047378
Study groupRoleWhat they receive
ACT Intervention GroupExperimentalBoth 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.
Receives: Behavioral: ACT Intervention Group
Control GroupOtherParticipants 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.
Receives: Other: control group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Parental Burnout

    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.

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

  2. Children's emotional and behavioral adjustment

    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).

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

Secondary outcomes (4)
  1. Parental Psychological flexibility

    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.

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

  2. Children's psychological flexibility

    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.

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

  3. Adaptive parenting behaviors

    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.

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

  4. Parent-Child Relationship Quality

    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.

    Measured: Change from baseline assessment to immediate and 3 months post-intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Jul 2025
  2. Study start22 Apr 2025
  3. Primary completion30 Apr 2027 (estimated)
  4. Study completion30 Apr 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Parallel Assignment; Repeated measures (baseline, post-intervention, and 3-month follow-up) 2-arm randomized controlled trial
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07047378
Sponsor's protocol ID
NTEC-2025-184
Status last verified
Jul 2025
First submitted
24 Jun 2025
Last updated
10 Jul 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: As participants were not asked to provide consent for sharing their individual data with external researchers, IPD cannot be made available.

Questions about this trial

What is this clinical trial studying?

A study testing ACT Intervention Group in people with Child Abuse and Parental Burnout, run by Chinese University of Hong Kong at 2 sites in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 10 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Yuen Yu CHONG, PhD ((852) 3943 0665, conniechong@cuhk.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Parental Burnout (time frame: Change from baseline assessment to immediate and 3 months post-intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jul 2025.

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