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Effectiveness of Self-Compassion Intervention on Enhancing Self-Compassion and Psychological Well-Being of Children With Attention Deficit/Hyperactivity Disorder

Not Applicable
Recruiting
Conditions
Self-Compassion
Psychological Well-Being
ADHD
Interventions
Behavioral: Self-Compassion Intervention
Registration Number
NCT06352801
Lead Sponsor
The University of Hong Kong
Brief Summary

The study aims to investigate the underlying mechanism between Attention Deficit/Hyperactivity Disorder traits (AD/HD traits) and psychological well-being through studying the role of perceived criticism, rejection sensitivity, self-compassion and growth mindset. It also aims to explore the effectiveness of self-compassion intervention on enhancing self-compassion and psychological well-being of children with AD/HD in Hong Kong. The study will contribute to the current understanding of the supportive measures for children with AD/HD, and hopefully help to mobilize more resources to preserve children with AD/HD's mental health.

The intervention program includes the following components:

Participants will be randomly assigned to the self-compassion intervention group or the waitlist control group. The intervention group consists of two parts: children training session and parent group sessions. All children participants will complete a total of 6 training sessions, and each session will last around 90 minutes. Parents of the children participants will also complete a total of 3 group sessions, and each session will last around 90 minutes.

To investigate the intervention effectiveness, children will be asked to complete a questionnaire assessing their levels of self-compassion, emotional regulation, as well as psychological well-being in terms of life satisfaction, positive and negative affect. Parents and teachers of participants will also be asked to complete a questionnaire covering children's emotional regulation, positive and negative affect. Questionnaire data collection will be conducted prior to the intervention (i.e., Time 1), immediately after the 6-session student and 3-session parent sessions (i.e., Time 2), and 2 months after the intervention (i.e., Time 3, a 2-month follow up). It takes approximately 20-30 minutes for children and parents to complete their questionnaires.

Study Objectives:

1. To investigate the underlying mechanism of the relationship between AD/HD traits and psychological well-being

2. To explore the effectiveness of self-compassion intervention on enhancing self-compassion and psychological well-being of children with AD/HD in Hong Kong

Hypotheses:

1. AD/HD traits negatively predicts psychological well-being

2. AD/HD traits positively predicts perceived criticism or rejection sensitivity

3. Perceived criticism or rejective sensitivity negatively predicts psychological well-being

4. Perceived criticism or rejective sensitivity mediates the relationship between AD/HD traits and psychological well-being

5. Self-compassion moderates the relationship between perceived criticism or rejection sensitivity and psychological well-being

6. Growth mindset moderates the relationship between perceived criticism or rejection sensitivity and psychological well-being

7. Children with AD/HD from self-compassion intervention group yield greater improvement in self-compassion, emotional regulation and psychological well-being, than waitlist-control group.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Upper primary students
  • Clinical diagnosis, suspected cases of AD/HD, or having AD/HD symptoms
  • Able to read, write and communicate in Chinese
Exclusion Criteria
  • Hearing, visual, or physical impairments that might hinder participation in the intervention
  • Clinical diagnosis and suspected cases of Autism Spectrum Disorder (ASD)
  • Prior or current participation in a psychotherapeutic treatment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Self-Compassion Intervention GroupSelf-Compassion InterventionThe intervention group consists of two parts: children training session and parent group sessions. All children participants will complete a total of 6 training sessions, and each session will last around 90 minutes. Parents of the children participants will also complete a total of 3 group sessions, and each session will last around 90 minutes. Participants will receive intervention in Phase 1.
Primary Outcome Measures
NameTimeMethod
Self-Compassion Scale for Children (SCS-C)Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)

A scale consisting of 12 self-report items assessing children's self-compassion \[Min. Value: 1; Max Value: 5 (with higher score indicating higher level of self-compassion)\]

Behavioural ratings on children's executive functionsDelayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)

Parents and teachers will be asked to complete Behaviour Rating Inventory of Executive Function, Second Edition (BRIEF2) measuring a range of executive functions, including emotional regulation \[Min. Value: 1; Max Value: 4 (with higher score indicating higher level of emotional regulation)\]

Positive and Negative Affect Schedule for Children (PANAS-C/P)Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)

The PANAS, is a self-reported adjective checklist that contains two 5-item subscales designed to measure positive and negative affect. Children, parents and teachers will be asked to complete the scale \[Min. Value: 1; Max Value: 5 (with higher score indicating higher level of positive and negative affect)\]

Student's Life Satisfaction Scale (SLSS)Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)

A scale consisting of 7 self-report items assessing children's life satisfaction \[Min. Value: 1; Max Value: 6 (with higher score indicating higher level of life satisfaction)\]

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The University of Hong Kong

🇭🇰

Hong Kong, Hong Kong

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