NCT07826702

Brief Summary

This pilot randomised controlled trial (RCT) aims to evaluate the feasibility, acceptability, and preliminary effects of combining a brief Nonviolent Communication (NVC) intervention with follow-up personalised AI-generated messages delivered daily via WhatsApp to improve child-parent relationships, parenting competence and family communication. A total of 60 parents of middle school students experiencing difficulties in family communication or recurrent conflict with their children will be recruited in Hong Kong and randomly assigned (in a 1:1 allocation ratio) to an intervention group or an attention control group. The intervention group will participate in two 2-hour NVC workshops, scheduled two weeks apart and delivered by the principal investigator, plus four weeks of personalised AI-generated NVC e-messages daily. The attention control group will receive weekly e-messages with healthy lifestyle tips for 6 weeks. Assessments for participants will be conducted at baseline (T0), post-workshop (T1, after the second session/two weeks after T0), and 12 weeks after baseline (T2). A process evaluation featuring quantitative ratings and open-ended questions will be conducted to explore participants' perceived benefits and subjective experiences.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
12mo left

Started Oct 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress1%
Oct 2026Sep 2027

First Submitted

Initial submission to the registry

September 14, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 17, 2026

Completed
14 days until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2027

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2027

Last Updated

September 23, 2026

Status Verified

September 1, 2026

Enrollment Period

9 months

First QC Date

September 14, 2026

Last Update Submit

September 20, 2026

Conditions

Keywords

Nonviolent CommunicationText MessagingRandomized Controlled TrialRelationship, Parent Child

Outcome Measures

Primary Outcomes (2)

  • Recruitment rate

    Recruitment rate is defined as the proportion of eligible or contacted candidates who actually agree to join the study (Number Enrolled / Number Eligible or Approached).

    Baseline (T0)

  • Retention rate

    Retention rate is defined as the percentage of randomised participants retained and assessed with valid primary outcome data.

    12-week assessment (T2, around 3 months after baseline)

Secondary Outcomes (4)

  • Child-Parent Relationship

    Baseline (T0), Post-workshop assessment (T1, 2 weeks after T0), and 12-week assessment (T2, around 3 months after T0).

  • Parenting Competence

    Baseline (T0), Post-workshop assessment (T1, 2 weeks after T0), and 12-week assessment (T2, around 3 months after T0).

  • Family function

    Baseline (T0), Post-workshop assessment (T1, 2 weeks after T0), and 12-week assessment (T2, around 3 months after T0).

  • Anxiety

    Baseline (T0), Post-workshop assessment (T1, 2 weeks after T0), and 12-week assessment (T2, around 3 months after T0).

Other Outcomes (1)

  • Perceived Benefits

    Post-workshop assessment (T1) and 12-week assessment (T2, around 3 months after T0)

Study Arms (2)

NVC Intervention Group

EXPERIMENTAL

Participants in the intervention group will receive two 2-hour NVC intervention workshops, scheduled two weeks apart and delivered in small groups (either online or face-to-face) by the PI, plus four weeks of daily personalised AI-generated NVC messages via WhatsApp.

Behavioral: Nonviolent Communication Intervention & Personalised E-messages

Attention Control Group

ACTIVE COMPARATOR

Participants in the attention control group will not receive any NVC intervention workshops during the study. They will receive regular healthy lifestyle information messages via WhatsApp for 6 weeks.

Behavioral: Healthy Lifestyle Tips

Interventions

The attention control group will receive an information pamphlet that encourages them to maintain a healthy diet, engage in regular physical activity, and practice weight control. Participants will receive weekly WhatsApp messages about healthy lifestyle tips for 6 weeks.

Attention Control Group

The intervention includes an introduction to NVC's four principles, the difference between observations and judgments, identifying and expressing feelings, taking responsibility for feelings and needs, and using positive action language when making requests. The intervention workshops will be offered in rolling monthly cycles for approximately three rounds over three months (two rounds will be online, and one will be face-to-face). Participants who miss the second session may attend an equivalent session in the second or third cycle. Between and following the sessions, participants will receive AI-generated, tailored messages via WhatsApp daily for four weeks that provide concise NVC tips and guide parents through NVC-style conversations with their adolescents.

NVC Intervention Group

Eligibility Criteria

Age32 Years - 59 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • \) parents aged 32-59 years with children attending middle school (approximately 12-17 years old) in Hong Kong;
  • \) scoring 3 or above in any item of the 3-item conflict subscale of the Network of Relationship Inventory (Furman \& Buhrmester, 2009);
  • \) able to read Chinese and use a smartphone to receive WhatsApp messages;
  • \) willingness to attend a two-session NVC intervention in group format.

You may not qualify if:

  • \) severe mental health problems requiring immediate specialist care or inability to provide informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Jockey Club Institute of Healthcare, Hong Kong Metropolitan University

Hong Kong, Hong Kong

Location

Study Officials

  • Yuying Sun, PhD

    Hong Kong Metropolitan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yuying Sun, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 14, 2026

First Posted

September 17, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

September 30, 2027

Last Updated

September 23, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

We are not sharing individual participant data (IPD) due to privacy concerns and limitations in participant consent. Although the data is de-identified, there remains a risk of re-identification, and participants were not explicitly consented for public data sharing. Aggregate results will be made available through publications and presentations to ensure transparency.

Locations