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Screen Time ExposureNCT07083661

Mindfulness-based Intervention and Young Children's Screen Time

A study testing Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE) in people with Screen Time Exposure, run by Hong Kong Metropolitan University at 1 site in Hong Kong.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This research proposal aims to explore the effectiveness of the mindfulness-based intervention (MBI) on reducing young children's screen time (ST) and caring parents' psychological and social issues in Hong Kong. Read more about this study

Who is it for?
Ages 2 years and olderHealthy volunteers can take part
Conditions the study is for
Screen Time Exposure
What is being tested?
Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteHong Kong
Study dates
20 Aug 2025to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • parent-child dyads resident in Hong Kong;
  • child being between 2 and 6- year; and
  • child with normal intellectual ability.

Who cannot join

  • children with major developmental problems, history of domestic violence, drug abuse, or mental illness in the family;
  • being unable to communicate and understand Cantonese as the intervention will be conducted in Cantonese; and
  • parent-child dyads previous participation in mindfulness-based training for less than 6 months.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Yuen Ling Leung, Doctor of Nursing contact

39708751

lleung@hkmu.edu.hk

Sze Him, Isaac Leung, PhD in Statistics contact

3943 9423

shleung@cuhk.edu.hk

Hong Kong1 site, 1 recruiting
  • Hong Kong Metropolitan University

    Hong Kong

    Yuen Ling LEUNG, (852)39708751

    Recruiting

Other trials in Hong Kong

About this study

Official title: Mindfulness-based Intervention on Parent Empowerment in Reducing Young Children's Screen Time (MORE): a Mixed Method Study

This research proposal aims to explore the effectiveness of the mindfulness-based intervention (MBI) on reducing young children's screen time (ST) and caring parents' psychological and social issues in Hong Kong.

Read the detailed description

The research design was a two-arm waitlist, randomised controlled study with a focus group interview with 60 participants. The intervention integrates the mindfulness-based component into a modified Hands-on Parent Empowerment-20 (HOPE-20) programme, and is named as MORE (i.e. Mindfulness-based intervention On parent empowerment in REducing children's screen time). The intervention consists of 6 weeks of MBI training, each lasting for 2 hours, led by an experienced certified mindfulness teacher. The intervention programme consists of three components: (1) skill part - 4 lessons talk about parenting skills (Praising, token system, response cost, planned ignorance, quiet zone); (2) skill part - 2 lessons talk about child-parent communication (building relationship, communication strategies); and (3) mindfulness part - mindfulness-based training. The primary outcomes are young children's ST and children's disruptive behaviour. Feasibility outcomes include recruitment rate, retention rate, and acceptability of the interventions. Secondary outcomes include parent-child relationships, parents' perceptions of their abilities to manage the demands of parenting, parental stress level, and social support adequacy. The proposal also includes plans for focus group interviews with participants to gather qualitative data. Analyses will include descriptive statistics, Pearson's chi-square test, Pearson's product-moment correlations, One-way ANOVA. A p-value < 0.05 will be taken as the level of statistical significant. The 95% Confidence interval (CI) around the differences will be calculated. For qualitative data, the results will be analyzed descriptively and narratively. The proposal highlights the potential of MBI for reducing young children's ST, as well as improving children-parent relationships, enhancing the efficacy and satisfaction level of the parents, and reducing the stress level of the parents.

Being tested
Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE)
Keywords
screen time exposure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE)Behavioural

    Participants will receive a 6-week MORE group training by integration of mindfulness-based component into a modified Hands-on Parent Empowerment-20 (HOPE-20) programme.

Study groups in NCT07083661
Study groupRoleWhat they receive
Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE)ExperimentalThe intervention consists of 6-session mindfulness-based intervention. Each session last for 2 hours. The training will be led by an experience certified mindfulness teacher.
Receives: Behavioral: Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE)
Waistlist control groupNo interventionParticipants will be required to maintain their usual daily activities without begin any mindfulness and skills programme for 6-week

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Screen time exposure - frequency

    Children's screen time exposure including frequency will be record in terms of times per week

    Measured: Baseline, week 6, week 18

  2. Screen time exposure - duration

    Duration will be record in terms of minutes

    Measured: Baseline, week 6, week 18

  3. Screen time exposure - nature and content

    Screen time exposure, nature, and content require the parent to provide the types and names of the shows watched by their young children.

    Measured: Baseline, week 6, week 18

  4. Screen time exposure - viewing behavior

    The parents are required to provide the information on young children's viewing behavior, including singing, role play, discussing issues or discussing the films and shows by selecting from the questionnaire.

    Measured: Baseline, week 6, week 18

  5. Change in parental stress level

    The Parenting Stress Index - short form. It is a 36-item 5-point Likert scale with three 12-item subscales. Each item is scored from 1 to 5 (1 = "strongly disagree", 5 = "strongly agree"). The lowest score is 36, and the highest score is 180. Higher scores indicated higher parenting stress, and the cutoff point is >90.

    Measured: Baseline, week 6, week 18

  6. Change in social support adquency level

    The Multidimensional Scale of Perceived Social Support Questionnaire is a 12-item questionnaire. Each item is scored from 1 to 7 (1 = "strongly disagree", 7 = "strongly agree"), the lowest score is 12 and the highest score is 84. A higher score defines higher social support from family, friends and significant others.

    Measured: Baseline, week 6, week 18

Secondary outcomes (2)
  1. Change in children disruptive behavior

    The Eyberg Child Behaviour Inventory is a 36-item questionnaire that consists of two subscales: the intensity scale and the problem scale. The intensity scale assesses the common child behavior problems frequency from 1 to 7 (1 = "never", 7 = "always"), and the problem scale assesses the extent to which the parents find the troublesome behavior in "yes" or "no". The lowest score is 36, and the highest score is 252. Higher scores indicate more child behavior problems.

    Measured: Baseline, week 6, week 18

  2. Change in parent-child relationships

    The Parenting Sense of Competence Scale is a 6-point Likert scale with 15-item. Each item is scored from 1 to 6 (1 = "strongly disagree", 6 = "strongly agree"), the lowest score is 15, and the highest score is 90. A higher score represents a better parent-child relationship

    Measured: Baseline, week 6, week 18

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jul 2025
  2. Study start20 Aug 2025
  3. Primary completion30 Sep 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07083661
Sponsor's protocol ID
RD/2025/1.7
Status last verified
Jul 2025
First submitted
4 Jul 2025
Last updated
8 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Mindfulness-based intervention on parent empowerment in reducing children's screen time (MORE) in people with Screen Time Exposure, run by Hong Kong Metropolitan University at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 8 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Yuen Ling Leung, Doctor of Nursing (39708751, lleung@hkmu.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Screen time exposure - frequency (time frame: Baseline, week 6, week 18). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jul 2026.

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