- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05480423
Online Mindfulness-based Intervention on Parents of Children With Attention Deficit/Hyperactivity Disorder (ADHDparent)
April 3, 2023 updated by: The Hong Kong Polytechnic University
A Pilot Study on Application of Online Technology for Mindfulness-based Intervention on Parents of Children With Attention Deficit/Hyperactivity Disorder
This project apply curriculum of online programme materials and structure for mindful parenting and caregiving.
It will include four modules (introductory mindfulness, mindful parenting, applying mindfulness in challenging moments, and advanced exercises for parents of children with special needs).
Each module will include short psychoeducation videos and audio mindfulness exercises that can be used in various web-based or application-based platforms.
A set of videos and audio exercises will be produced for the core program materials.
One study of online mindful parenting program reported a low completion rate below 30%, showing the significance of weekly video or phone contact by professionals in program engagement.
Although web-based or application-based mindfulness intervention have become popular, very limited effort has been developed for applying mindfulness in parenting and caregiving using technology.
Only two published studies on online mindfulness-based intervention for parents are identified.
Objectives of the study are: 1. Investigate the effects of online mindfulness-based intervention for parents of children with Attention Deficit/Hyperactivity Disorder.
2. Validate the protocol of the programme and explore the needs to make refinements of the programme based on the quantitative outcome and qualitative interview analyses
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Hong Kong, Hong Kong
- Hong Kong Polytechnic University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- parents whose children are between 6 and 18 years old and diagnosed with Attention Deficit/Hyperactivity Disorder
- parents can understand and speak Cantonese Chinese, and
- participants should be the primary caretaker of the children in the last one year
Exclusion Criteria:
- parents who were diagnosed with psychosis, developmental disabilities, or cognitive impairment, which may present difficulties in comprehending the content of the program,
- parents have had prior experience in any 8-week Mindfulness-Based Stress Reduction/Mindfulness-Based Cognitive Therapy or equivalent program.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Online mindfulness-based intervention
The online programme lasts for 28 days.
Parents will receive the links of daily mini-lectures that introduced basic principles in mindfulness and mindful parenting, audio files of guided mindfulness practice, and exercises that facilitates parents to integrate mindfulness in their daily lives.
The total time spent in each session will be around 15 to 20 minutes.
Weekly meeting will be arranged with mindfulness instructor and participants.
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1. Psychoeducation video on mindfulness and mindful parenting.
2. Audio files of mindfulness exercises including mindfulness of breath, body scan, mindful stretching, mindfulness of soles of the feet, befriending exercises.
3. Informal mindfulness exercises by applying mindfulness in daily lives
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No Intervention: Waitlist controlled group
Participants will be offered same intervention three months later
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental stress
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
|
The Parenting Stress Index Short Form (PSI-SF) will be used to measure parental stress (Abidin, 1995; Lam, 1999).
A total of 36 items covers three dimensions parental distress, parent-child dysfunctional interaction, and difficult child.
Parents will rate the items on a 5-point Likert scale from strongly disagree (1) to strongly agree (5).
Total score from 36 to 180.
The higher the score, the higher the level of stress.
|
Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parent Anxiety
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
|
The anxiety subscale of the Hospital Anxiety and Depression Scale (HADS-A) will be used to measure affective and behavioural symptoms of anxiety (Zigmond & Snaith, 1983).
Parents will rate the items on a 4-point Likert scale from 0 to 3, with anchors varying between items (e.g., from "Very much indeed" to "Not at all").
Total score from 0 to 21.
The higher the score, the higher the level of anxiety.
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Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
|
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Parent depression
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
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The 10-item version of the Center for Epidemiologic Studies Depression Scale (CES-D) will be used to measure affective symptoms of depression (Radloff, 1977).Parents will rate the items on a 4-point Likert scale from none of the time (0) to most of the time (3).
Total score from 0 to 30.
The higher the score, the higher the level of depression.
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Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
|
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Family Functioning
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
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The Family Adaptation, Partnership, Growth, Affection, Resolve scale (APGAR) will be used to measure the satisfaction of perceived family functioning (Smilkstein et al., 1982).Parents will rate the items on a 3-point Likert scale from hardly ever (0) to almost always (2). total score from 0 to 10.
The higher the score, the higher the level of family functioning.
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Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
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Parent Quality of Sleep
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
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The self-administered version of the Insomnia Severity Index (ISI) will be used to assess sleeping quality (Morin, 1993).
The 7-item scale assesses the severity of initial, middle, and late insomnia, distress about sleep difficulties, interference of insomnia with daytime functioning, and notice of sleep problems by others.
Parents will rate the items on a 4-point Likert scale from not at all (0) to extremely (2).
Total score 0 to 14.
The higher the score, the higher the severity of sleep difficulties.
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Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up
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Child Attention Deficit/Hyperactivity Disorder (ADHD) symptomology
Time Frame: Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
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The Strengths and Weaknesses of ADHD Symptoms and Normal Behaviors (SWAN) Rating Scale will be used to measure the similarity or differences between a child's attention skills and those of the general population (Swanson et al., 2012).
A total of 18 items represents a range of behavioural characteristics.
Parents will be asked to compare their child to other same-age children and rate their child on a 7-point Likert scale from far below average (-3) to far above average (3).
Total score from -54 to 54.
The lower the score, the higher the severity of ADHD symptoms.
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Change from pre-intervention, to 1-month follow-up, and to 3-month follow-up.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Herman Hay Ming Lo, PhD, Hong Kong Polytechnic University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 15, 2022
Primary Completion (Actual)
March 15, 2023
Study Completion (Actual)
March 15, 2023
Study Registration Dates
First Submitted
July 27, 2022
First Submitted That Met QC Criteria
July 27, 2022
First Posted (Actual)
July 29, 2022
Study Record Updates
Last Update Posted (Actual)
April 5, 2023
Last Update Submitted That Met QC Criteria
April 3, 2023
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ADHDparent
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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