NCT06255405

Brief Summary

Suboptimal psychological well-being in children can have substantial negative effects on their physical health, academic performance, and lifelong health. Preliminary evidence supports that self-compassion have positive impacts on psychological well-being in elderly, adults, and adolescents, but there is apparently lack of this kind of evidence in children. Involvement of parents in the program potentially optimize the effects, this study thus designs a dyadic parent-child self-compassion program (DPC-SC) and aim to examine its effects on children's psychological well-being.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
96

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2024

Typical duration 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

February 4, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 13, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

April 1, 2024

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 6, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 6, 2026

Completed
Last Updated

August 25, 2026

Status Verified

August 1, 2026

Enrollment Period

1.9 years

First QC Date

February 4, 2024

Last Update Submit

August 22, 2026

Conditions

Keywords

psychological well-being; self-compassion; childrendyadic

Outcome Measures

Primary Outcomes (1)

  • Psychological well-being (child)

    Chinese version of the Psychological Well-Being Scale (C-PWBS)

    at Baseline, immediately after intervention, 12-week follow-up

Secondary Outcomes (4)

  • Perceived stress levels (Child)

    at Baseline, immediately after intervention, 12-week follow-up

  • Self-compassion levels (Child)

    at Baseline, immediately after intervention, 12-week follow-up

  • Self-compassion levels (parents)

    at Baseline, immediately after intervention, 12-week follow-up

  • Level of mindful parenting (parents)

    at baseline, immediately after the intervention, and 12-week follow up

Study Arms (2)

Experimental: Intervention group

EXPERIMENTAL

Dyadic parent-child self-compassion program will be provided.

Behavioral: Self-compassion

Waitlist control group

NO INTERVENTION

Participants in the control group will be instructed to live their lives as usual, no intervention will be imposed during study period. They will be provided with the program after the study.

Interventions

Self-compassionBEHAVIORAL

The dyadic parent-child self-compassion program is designed by the research team and validated by a panel of experts. It includes 5 weekly sessions. Each session lasts for 60 minutes. The dyads will be guided to do self-compassion practices (e.g. affectionate breathing, compassionate letters to oneself etc). Didactic topics, inquiry, and home practices are also involved.

Experimental: Intervention group

Eligibility Criteria

Age7 Years - 11 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Can communicate in Cantonese.

You may not qualify if:

  • Have emotional dysregulation
  • Have past history of mental illness
  • Recently experience trauma
  • Are in an acute health crisis
  • Is the primary caretaker of the children
  • Is willing to interact and do the practices with their children
  • Can communicate in Cantonese
  • Commit to attend all sessions
  • Have emotional dysregulation
  • Have past history of mental illness
  • Recently experience trauma
  • Are in an acute health crisis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hong Kong Metropolitan University

Hong Kong, Hong Kong

Location

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Wai Man Sin, Master

    Hong Kong Metropolitan University

    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
SPONSOR INVESTIGATOR
PI Title
PhD student

Study Record Dates

First Submitted

February 4, 2024

First Posted

February 13, 2024

Study Start

April 1, 2024

Primary Completion

February 6, 2026

Study Completion

February 6, 2026

Last Updated

August 25, 2026

Record last verified: 2026-08

Locations