Nonviolent Communication for Parents
Effectiveness of Group-based Nonviolent Communication Interventions for Improving Mental Well-being in Parents: a Randomised Controlled Trial
1 other identifier
interventional
172
1 country
1
Brief Summary
This randomised controlled trial (RCT) aims to evaluate the effectiveness of face-to-face Nonviolent Communication (NVC) intervention in improving parents' mental well-being and NVC skills, reducing parenting stress, depression and anxiety symptoms, and child emotional and behavioural problems. A total of 172 parents with primary-school-age children will be recruited and randomly assigned to an intervention group or a waitlist control group. The intervention group will receive six weekly 1.5-hour face-to-face NVC training sessions delivered by trained social workers. Five to ten social workers will be trained by professional NVC trainers through a train-the-trainer workshop, including three sessions. Each social worker will be assessed before (TTT1), after (TTT2) the workshops and 10 months (TTT3). Assessments for participants will be conducted at baseline (T1), immediately post-intervention (T2), and at three-month follow-up (T3). After completing the assessments, the waitlist control group will receive the same sessions. Qualitative interviews will be conducted to explore participants' experiences and perceptions of NVC.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable anxiety
Started May 2025
1 active site
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
April 17, 2025
CompletedFirst Posted
Study publicly available on registry
April 24, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
September 17, 2025
September 1, 2025
1.1 years
April 17, 2025
September 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Well-being
The Short Warwick-Edinburgh Mental Well-being Scale (SWEMWS) is a 7-item scale for assessing mental health in non-clinical populations. Using a 5-point Likert scale (1 = none of the time, 5 = all the time), the total score is calculated by summing all seven items. The Chinese version showed good validity and reliability in the investigators' previous study. The congeneric reliability was 0.85 and the test-retest reliability was 0.70.
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
NVC skills
The measure of NVC skills was developed based on a 16-item scale that represents the four principles of NVC skills. Each item is rated on a 5-point scale ranging from 0 = never to 5 = always. The average score is calculated, with higher scores indicating better NVC skills. Cronbach's alpha was 0.82 in the investigators' pilot study.
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
Secondary Outcomes (4)
Parenting stress
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
Depressive symptoms
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
Anxiety
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
Child emotional and behavioural problems
T1: Baseline; T2: Immediate post-intervention; T3: 3 months post-T2
Other Outcomes (1)
Train-the-trainer outcome
T1: Baseline, before the workshop; T2: Immediate after the workshop; T3: 10 months after baseline.
Study Arms (2)
Receiving NVC Interventions
EXPERIMENTALParticipants in the intervention group will receive six weekly 1.5-hour face-to-face NVC training sessions delivered by trained social workers.
Wailist Control Group
NO INTERVENTIONThe waitlist control group will not receive any training before all the assessments have been done by both groups. The wailist control group will receive NVC training sessions after all assessments. During the whole study period, these participants can access usual medical services, whether related or unrelated to mental health needs.
Interventions
The intervention will be conducted by social workers who will be trained by professional NVC trainers through a train-the-trainer workshop, including six sessions. The interventions include an introduction to four fundamental principles of NVC, distinguishing observations from evaluations, identifying and expressing feelings, taking responsibility for feelings and needs, and using positive action language to make requests. Each session will feature a review of the previous session, a warm-up game and an exercise to consolidate the learning of the concepts. The intervention sessions will also include group discussions and debriefing sessions on parents' experiences of practising NVC.
Eligibility Criteria
You may qualify if:
- \) parents aged 24-59 years with children of primary school age;
- \) with mild to severe depressive symptoms (score \>5 on the Patient Health Questionnaire (PHQ)-9) (Kroenke et al., 2001) and/or mild to severe anxiety symptoms (score \>5 on the General Anxiety Disorder (GAD)-7) (Spitzer et al., 2006); and
- \) Hong Kong residents who can understand Cantonese.
You may not qualify if:
- \) under psychiatric treatment, psychotherapy groups and are classified as unstable cases based on the judgment of the recruiting social workers;
- \) participating in other related parenting programmes.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Jockey Club Institute of Healthcare of Hong Kong Metropolitan University
Hong Kong, Hong Kong
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Grace Yuying Sun
Hong Kong Metropolitan University
Central Study Contacts
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
April 17, 2025
First Posted
April 24, 2025
Study Start
May 1, 2025
Primary Completion (Estimated)
May 31, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
September 17, 2025
Record last verified: 2025-09
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.