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A randomised controlled trial comparing MYmind with waitlist control among Chinese children with ADHD and their parents

A randomised controlled trial comparing MYmind with waitlist control among Chinese children with ADHD and their parents

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016591
Enrollment
Unknown
Registered
2018-06-11
Start date
2018-06-28
Completion date
Unknown
Last updated
2018-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder (ADHD)

Interventions

Sponsors

The D. H. Chen Foundation, Hong Kong SAR
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 80 Years

Inclusion criteria

Inclusion criteria: Participants will include children and one parent of each child. However, the other parent of the same child is also welcome to participate in the mindfulness course but only their course attendance will be recorded to reduce the burden of the participating families. The inclusion criteria will be: 1) children aged 8 to 18 years with psychiatrist or psychologist diagnosed ADHD according to the Diagnostic and Statistical Manual of Mental Disorders - 5 (DSM-5) diagnostic criteria; and 2) with normal intellectual ability such that they can understand the materials delivered in MYmind and that they can complete home practice each week; and 3) children either not taking any medication or taking a stable dosage of the same medication for ADHD for at least 3 months prior to study enrolment and having no plan for changing medication during the study period.

Exclusion criteria

Exclusion criteria: The exclusion criteria of children and parents will be: 1) being unable to communicate and understand Chinese language as the intervention will be conducted in Chinese; 2) the child having comorbid conduct/behavior problems which are so severe that, during intake, the interaction between parent and assessor is interrupted by the child within 2 minutes, which makes it impossible for the child to participate in a group training. Instructions of this criterion are adapted from the Autism Diagnostic Observation Schedule (ADOS) and will be provided to the assessor to facilitate to examine whether the child may be or may not be able to participate in a group training in addition to the clinicians expertise; 3) having a medical or mental health condition rendering him/her to be incapable of participating in the study; and 4) previous participation in mindfulness-based training.

Design outcomes

Primary

MeasureTime frame
The attention score of the subtest Sky Search of TEA-Ch (for children);

Secondary

MeasureTime frame
Creature Counting, Opposite Worlds, and Code Transmission subtests of TEA-Ch (for children);Child attention network test (ANT) (for children);The Strengths and Weaknesses of ADHD Symptoms and Normal Behaviours (SWAN) Rating Scale (for children);The Eyberg Child Behaviour Inventory (ECBI) (for children);The Child and Adolescent Mindfulness Measure (CAMM) (for children);WHO-5 Well-being Index (WHO-5) (for children and parents);Child and Youth Resilience Measure (CYRM);The Child Behaviour Checklist (CBCL);Family APGAR index;Health service utilization (for children and parents);Parenting Stress Index (PSI) (for parents);Rumination Response Scale (RRS) short form (for parents);Adult ADHD Self-Report Scale (ASRS);

Countries

China

Contacts

Public ContactProf. Samuel Yeung Shan WONG

4/F, School of Public Health and Primary Care, Prince of Wales Hospital, Shatin, N.T., Hong Kong, China

yeungshanwong@cuhk.edu.hk+852 22528774

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026