Comparing parent-only and parent-child group programs to reduce aggression in Hong Kong schoolchildren

ISRCTN ISRCTN17582705
DOI https://doi.org/10.1186/ISRCTN17582705
Sponsor City University of Hong Kong
Funder Research Grants Council, University Grants Committee
Submission date
30/01/2026
Registration date
02/02/2026
Last edited
02/02/2026
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Background and study aims
Aggressive behaviour and bullying are serious problems for some schoolchildren. This research study tested two different types of group programs designed to help parents manage their child's aggression. We wanted to see if a program involving both parents and children together was more effective than a program for parents only.

Who can participate?
We invited children aged 5-12 years from Hong Kong primary schools who showed higher levels of aggressive behaviour, along with one of their parents.

What does the study involve?
Families were randomly placed into one of three groups: 1) Parent-only group (7 weekly sessions), 2) Parent-child group (7 weekly sessions together), or 3) A waiting list group (no immediate sessions). The sessions taught parents about different types of aggression and skills to improve parenting and the parent-child relationship. Families filled out questionnaires before, immediately after, and 6 months after the program.

What are the possible benefits and risks of participating?
Potential benefits included learning new parenting skills and possibly reducing child aggression. A potential risk was the time commitment required. All information was kept confidential.

Where is the study run from?
Sessions were held at participating schools in Hong Kong.

When is the study starting and how long is it expected to run for?
The study recruited families between July and December 2022. The intervention lasted 7 weeks, with follow-up 6 months later.

Who is funding the study?
The Research Grants Council of Hong Kong (General Research Fund, project number 11600020).

Who is the main contact?
Dr Annis Lai Chu Fung (annis.fung@cityu.edu.hk)

Contact information

Dr Annis Lai Chu Fung
Principal investigator, Public, Scientific

Department of Social and Behavioural Sciences, City University of Hong Kong
Hong Kong
000
Hong Kong

ORCiD logoORCID ID 0000-0002-5920-4003
Phone +852-34422923
Email annis.fung@cityu.edu.hk

Study information

Primary study designInterventional
AllocationRandomized controlled trial
MaskingOpen (masking not used)
ControlActive
AssignmentParallel
PurposeTreatment
Scientific titleA randomized controlled trial on the effectiveness of parent-only and parent-child conjoint group interventions in reducing reactive and proactive aggression among schoolchildren in Hong Kong
Study objectivesThis randomized controlled trial (RCT) aimed to develop and evaluate the effectiveness of social learning theory-based group interventions designed to reduce reactive and proactive aggression in schoolchildren by enhancing parental efficacy and improving parenting styles.

Primary Objective:
To compare the effectiveness of a parent-only intervention, a parent-child conjoint intervention, and a waitlist control group in reducing children's reactive aggression, proactive aggression, and general aggression over time (baseline, post-intervention, and 6-month follow-up).

Secondary Objective:
To examine the impact of both interventions on key parenting constructs, including parenting practices (positive parenting, inconsistent discipline, poor supervision) and parenting styles (warmth, control, guan).
Ethics approval(s)

Approved 27/03/2020, Human Subjects Ethics Sub-Committee (Research Grants & Contracts Office, City University of Hong Kong, Hong Kong, 000, Hong Kong; +852 34426856; roger@cityu.edu.hk), ref: 3-12-202003-02

Health condition(s) or problem(s) studiedChildhood aggression; Reactive aggression; Proactive aggression; Behavioral problems
InterventionThis is a three-arm, parallel-group, randomized controlled trial with a waitlist control condition.

Shortlisted families who meet the inclusion criteria are enrolled and randomly assigned to one of three conditions using a random number sequence:
1. Parent-Only Intervention Group
2. Parent-Child Conjoint Intervention Group
3. Waitlist Control Group

Both active interventions consist of seven weekly sessions, each lasting two hours, held on Saturdays at the participants' schools. Sessions are led by two registered social workers with specific training and experience. The intervention is based on Social Learning Theory and targets the distinct features of reactive aggression (e.g., hostile attribution bias, poor anger control) and proactive aggression (e.g., lack of empathy, reward-driven behavior).

Parent-Only Group: One parent from each family attends the sessions. Content focuses on psychoeducation about aggression subtypes, enhancing awareness of parenting style impacts, and training in skills to manage child aggression (e.g., reducing hostile attribution, facilitating emotion regulation, enhancing empathy and perspective-taking). Techniques include role-play, group discussion, and reflective feedback. Parents are assigned weekly behavioral tasks to practice at home.

Parent-Child Conjoint Group: One parent and their child attend the sessions together. The content mirrors the parent-only curriculum but is delivered interactively, with joint activities, role-plays, and real-time coaching of parenting skills within the parent-child dyad. This allows for direct modeling, immediate feedback, and practice of new relational dynamics.

Waitlist Control Group: Families in this group receive no intervention during the study period but complete all assessments. They are offered the opportunity to join the parent-only group in the following semester.
Intervention typeBehavioural
Primary outcome measure(s)
  1. Child-reported Aggression Score measured using Reactive-Proactive Aggression Questionnaire (RPQ) at Baseline (T0), Post-treatment (T1), and 6-month follow-up (T2)
Key secondary outcome measure(s)
Completion date31/08/2023

Eligibility

Participant type(s)
Age groupChild
Lower age limit5 Years
Upper age limit12 Years
SexAll
Target sample size at registration200
Total final enrolment166
Key inclusion criteria1. Child enrolled in grades 1-6 at a participating Hong Kong elementary school
2. Child scored above the school median on the Reactive-Proactive Aggression Questionnaire (RPQ)
3. At least one parent willing to attend a weekly 2-hour group session for 7 weeks
4. Family is local Hong Kong Cantonese-speaking
Key exclusion criteriaFormal diagnosis of intellectual disability, dyslexia, or autism spectrum disorder
Date of first enrolment01/07/2022
Date of final enrolment31/12/2022

Locations

Countries of recruitment

  • Hong Kong

Study participating centres

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot expected to be made available
IPD sharing plan

Editorial Notes

02/02/2026: Trial's existence confirmed by City University of Hong Kong.