NCT05977114

Brief Summary

The goal of this clinical trial is to learn about the effects of a family conflict intervention in Chinese New Arrival families in Hong Kong. The main questions it aims to answer are:

  • Is the family conflict intervention group more effective to improve adaptive parent-child conflict resolution skills compared to the control group?
  • Is the family conflict intervention group more effective to reduce parent-child conflicts compared to the control group?
  • Is the family conflict intervention group more effective to improve adaptive parental conflict resolution skills compared to the control group?
  • Is the family conflict intervention group more effective to enhance family harmony compared to the control group?
  • Is the family conflict intervention group more effective to enhance family resilience compared to the control group? Participants will be randomly assigned to one of the two groups: the family conflict intervention group and the handcraft-making group. For each group, parents will participate in 3 sessions independently, children will participate in 2 sessions independently, and parents and children will jointly participate in 1 session. Each session takes around 2 hours, and it takes 4 weeks to complete the full intervention. The family conflict intervention sessions include an introduction to the occurrence of family conflicts, communication skills training to prevent and address conflicts, and role play to practice the skills, etc. Researchers will compare the family conflict intervention group and the handcraft-making group to see if the family conflict intervention group is effective in promoting conflict resolution skills, reducing family conflicts, and enhancing family resilience.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
456

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 28, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 4, 2023

Completed
28 days until next milestone

Study Start

First participant enrolled

September 1, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2024

Completed
Last Updated

March 5, 2025

Status Verified

March 1, 2025

Enrollment Period

8 months

First QC Date

July 28, 2023

Last Update Submit

March 1, 2025

Conditions

Outcome Measures

Primary Outcomes (5)

  • Parent-child conflicts

    Parent-child conflicts are measured by the frequency and intensity of parent-child conflicts (Yau \& Smetana, 1996). Possible scores for conflict frequency range from 0 (not at all) to 4 (4 times or above). A higher score indicates a higher level of parent-child conflict frequency. Possible scores for conflict intensity range from 1 (none) to 5 (severe). A higher score indicates more severe parent-child conflicts.

    Baseline, 4 weeks, 8 weeks

  • Parent-child conflict resolution

    Parent-child conflict adaptive resolution strategy is measured by the subscale of the Parent-Child Conflict Response Strategy Scale (Sun, 2019). The four items are each rated on a five-point scale, which is from 1 (never) to 5 (always). A higher score indicates a higher level of adaptive parent-child conflict resolution.

    Baseline, 4 weeks, 8 weeks

  • The Chinese version of the Rahim Organizational Conflict Inventory-II

    Couple conflict and problem-solving will be measured by the subscale of the Chinese version of the Rahim Organizational Conflict Inventory-II (ROC-II; Rahim, 1983; Chang \& Lu, 2007). The subscale includes 7 items. Each item is rated on a five-point scale. A higher score indicates a higher level of adaptive couple conflict resolution.

    Baseline, 4 weeks, 8 weeks

  • Family Harmony Scale

    Family Harmony will be measured by the Family Harmony Scale (Fabrizio et al., 2015). The scale includes 8 items. Each item is rated on a five-point scale. A higher score indicates a higher level of family harmony.

    Baseline, 4 weeks, 8 weeks

  • Family Resilience Quetionnaire

    Family Resilience will be measured by the Walsh Family Resilience Questionnaire (Walsh, 2015). We selected 9 representative questions from the original questionnaire for our study. Each item is rated on a five-point scale. A higher score indicates a higher level of family resilience.

    Baseline, 4 weeks, 8 weeks

Study Arms (2)

4Rs Group

EXPERIMENTAL
Behavioral: family conflict intervention group

4As Group

ACTIVE COMPARATOR
Behavioral: handicraft-making group

Interventions

The family conflict preventive intervention includes the introduction to the occurrence of family conflicts, communication skills training, and role play to practice the skills.

4Rs Group

The group involves handicraft-making.

4As Group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Parents who have newly arrived in Hong Kong for less than seven years, and their children who are studying in primary school grade 4 to secondary school form 3; or
  • New arrivals who have settled in Hong Kong for less than seven years and are studying in primary school grade 4 to secondary school form 3, and their parents; and
  • Parents and children must live together; and
  • Parents and children must participate together

You may not qualify if:

  • Self-reported serious emotional or mental illness by parent or child, or
  • Children with special learning needs

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

International Social Service Hong Kong Branch

Hong Kong, China

Location

Study Officials

  • Xiaonan Nancy YU, Doctoral

    City University of Hong Kong

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 28, 2023

First Posted

August 4, 2023

Study Start

September 1, 2023

Primary Completion

April 30, 2024

Study Completion

June 30, 2024

Last Updated

March 5, 2025

Record last verified: 2025-03

Locations