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

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

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
17 days until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2024

Completed
Last Updated

February 13, 2024

Status Verified

February 1, 2024

Enrollment Period

6 months

First QC Date

February 4, 2024

Last Update Submit

February 4, 2024

Conditions

Keywords

psychological well-being; self-compassion; children

Outcome Measures

Primary Outcomes (1)

  • Psychological well-being (child)

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

    Baseline, immediately after intervention

Secondary Outcomes (3)

  • Perceived stress levels (Child)

    Baseline, immediately after intervention

  • Self-compassion levels (Child)

    Baseline, immediately after intervention

  • Self-compassion levels (parents)

    Baseline, immediately after intervention

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

Age8 Years - 9 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Study in Primary three or four.
  • 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

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Wai Man Sin, MN

    Hong Kong Metropolitan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 4, 2024

First Posted

February 13, 2024

Study Start

March 1, 2024

Primary Completion

September 1, 2024

Study Completion

September 1, 2024

Last Updated

February 13, 2024

Record last verified: 2024-02