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Not yet recruitingNCT07092787Updated Jul 30, 2025

Reducing Smartphone Overuse for Adolescents With Attention-Deficit Hyperactive Disorder

An interventional study of Smartphone-based behavioral intervention and Self-monitoring of smartphone use in Attention Deficit Hyerpactivity Disorder and Smartphone Addiction, sponsored by Education University of Hong Kong. Not yet recruiting. Open to participants aged 12 Years to 17 Years. Per ClinicalTrials.gov, last updated 2025-07-30.

Sponsored by Education University of Hong Kong · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
12 Years to 17 Years
Sex
All
01

Study summary

This study will develop and evaluate a smartphone-based behavioral intervention for adolescents with Attention-Deficit Hyperactive Disorder (ADHD) and smartphone overuse in Hong Kong. The main questions it aims to answer are:

  • Can a smartphone-based intervention lower self-reported smartphone dependence and objective smartphone usage?
  • Can a smartphone-based intervention lower parent-rated and self-rated ADHD symptoms?
  • Are there differences in electroencephalogram (EEG) in the smartphone salient vs smartphone non-salient conditions after intervention?

Adolescent participants will:

  • report weekly smartphone use patterns based on app screencap for 12 weeks
  • complete online surveys on smartphone dependency and ADHD symptoms for 3 times
  • receive 10-minute EEG recordings to gather resting-state EEG data in a natural and relaxing state for 3 times

Parent participants will:

  • provide a valid clinical report to confirm the adolescent's diagnosis of ADHD
  • complete online surveys to report on the adolescent's smartphone usage and ADHD symptoms for 3 times
02

Conditions studied

  • Attention Deficit Hyerpactivity Disorder
  • Smartphone Addiction
03

In context

Internet Addiction Disorder

170 studies on the registry are indexed under Internet Addiction Disorder; 49 are open to participants now.

This study's planned enrollment of 120 is above the median of 88 across 95 interventional studies indexed under Internet Addiction Disorder.

Browse Internet Addiction Disorder studies →

Lead sponsor

Education University of Hong Kong is the lead sponsor of 35 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • full-scale IQ above 85
  • right-handedness to control for hemispheric dominance
  • a confirmed diagnosis of ADHD
  • ratings of current symptoms of ADHD on the Strengths and Weaknesses of Attention Deficit Hyperactivity Disorder Symptoms and Normal Behaviour Scale
  • on a stable dose of ADHD medication for at least 4 weeks prior to trial entry or was taking no medication, with no plan to start or change medication type or dosage for the duration of the study
  • over 2 hours of daily smartphone use within the last 4 weeks excluding educational apps
  • a total score on the Smartphone Addiction Scale - Short Version (SAS-SV) above 31 and 33 for male and female adolescents, respectively

Exclusion criteria

Exclusion Criteria:

  • severe physical or sensory disabilities that may alter the participation in the intervention
  • major depressive episode, bipolar disorder, substance abuse/dependence within the last 6 months
  • significant neurological conditions (e.g., epilepsy, traumatic brain injury) that could affect cognitive and behavioral functioning
  • concurrent participation in other ADHD interventions (e.g., clinical trials) excluding standard care
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Smartphone Intervention

    The treatment group will receive a 12-week individualized smartphone-based behavioral intervention based on the following strategies. They will be contacted once a week to collect the objective smartphone use patterns and check for compliance of the intervention strategies.

    Behavioral: Smartphone-based behavioral intervention

  • Placebo comparator
    Control

    The control group will receive information about the known benefits and risks of SO and activate their smartphones' screentime monitoring setting. They will be contacted once a week to collect the objective smartphone use patterns, but they will self-monitor their smartphone usage.

    Other: Self-monitoring of smartphone use

Interventions

  • BehavioralSmartphone-based behavioral intervention

    The proposed study will use a behavioral smartphone-based intervention in a 12-week RCT among clinically diagnosed ADHD adolescents in Hong Kong. Guided by a conceptual framework on SO in ADHD, we will implement specific strategies that counter the potentially addictive qualities of smartphones using built-in smartphone functions that have been previously shown to be effective.

  • OtherSelf-monitoring of smartphone use

    Participants will receive information about the known benefits and risks of SO and activate their smartphones' screentime monitoring setting. They will receive weekly reminders to submit their smartphone usage data.

06

What researchers measure

Primary outcomes

  1. Minutes of smartphone use

    Objective smartphone use data will be collected via smartphone apps (e.g., "ScreenTime" on Apple or "Digital Wellbeing" on Android) to trace the pattern of smartphone use of each participant. Participants will send screenshots of the minutes of smartphone use over the previous 7 days on their phones.

    Time frame: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 weeks, and 12 months

  2. Categories of smartphone use

    Objective smartphone use data will be collected via smartphone apps (e.g., "ScreenTime" on Apple or "Digital Wellbeing" on Android) to trace the pattern of smartphone use of each participant. Participants will send screenshots of the distribution of minutes spent according to categories of use (social networking, games, entertainment, productivity, etc.) over the previous 7 days on their phones.

    Time frame: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 weeks, and 12 months

  3. Number of screen unlocks or "pickups"

    Objective smartphone use data will be collected via smartphone apps (e.g., "ScreenTime" on Apple or "Digital Wellbeing" on Android) to trace the pattern of smartphone use of each participant. Participants will send screenshots of the number of screen unlocks or "pickups" over the previous 7 days on their phones.

    Time frame: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 weeks, and 12 months

  4. Number of notifications

    Objective smartphone use data will be collected via smartphone apps (e.g., "ScreenTime" on Apple or "Digital Wellbeing" on Android) to trace the pattern of smartphone use of each participant. Participants will send screenshots of the number of notifications received over the previous 7 days on their phones.

    Time frame: Baseline, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 weeks, and 12 months

  5. Smartphone dependence

    To allow for comparisons with existing studies, we will use the Smartphone Addiction Scale - Short Version validated in Hong Kong, which was designed for the assessment of smartphone dependence and showed good reliability and validity. The scale has ten items, such as "Missing planned work due to smartphone use" and "I will never give up using my smartphone even when my daily life is already greatly affected by it". Each item was measured by 6-point scales, from 1= "strongly disagree" to 6 = "strongly agree". Total score on the scale will be used to assess the degree of each participant's smartphone dependence, with suggested cut-off values of smartphone overuse for male and female was 31 and 33, respectively.

    Time frame: Baseline, 13 weeks, and 12 months

Secondary outcomes

  1. ADHD symptoms

    Parents will rate their child's behaviors on a 7-point scale using the Strengths and Weaknesses of Attention Deficit Hyperactivity Disorder Symptoms and Normal Behaviour Scale, which rephrased the 18 ADHD items of the DSM into neutral or positive statements. Scores of each statement range from -3 (far above average) to +3 (far below average), anchoring on normative behavior in age-matched adolescents. Two subscales on inattention and hyperactivity-impulsivity symptoms can be derived. Adolescents will also self-rate their ADHD symptoms.

    Time frame: Baseline, 13 weeks, and 12 months

  2. Resting-state EEG frequency

    During the EEG recording process, adolescent participants will be asked to relax and avoid swallowing and movements that may cause artifacts. For 5 min of recording, participants will look at a blank piece of paper on the table. For another 5 min of recording, they will look at their own smartphone, face-down with notifications and sound turned off, on the table. The order will be counterbalanced across participants. The target outcome measures are alpha (8-12Hz) and delta (1-4Hz) EEG frequency bands.

    Time frame: Baseline, 13 weeks, and 12 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Yum YN, Li X, Poon KY, Leung CH. Reducing smartphone overuse for adolescents with attention-deficit hyperactive disorder: study protocol for a randomized controlled trial. BMC Psychiatry. 2025 Oct 31;25(1):1043. doi: 10.1186/s12888-025-07493-w. PubMed 41174591 ↗

Individual participant data

Plan to share: No — Aggregate and anonymized data will be shared in open access publications, but individual participant data will not shared to protect the privacy of the participants, as stipulated in the ethical review approval.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07092787
Lead sponsor
Education University of Hong Kong
Responsible party
YUM Yen Na Cherry (Associate Professor, Education University of Hong Kong) — Principal investigator
First posted
Jul 30, 2025
Start date
Sep 2025 (estimated)
Primary completion
Mar 2028 (estimated)
Completion
Jun 2028 (estimated)
Last update
Jul 30, 2025

Study contacts

Yen Na Yum
Contact
yyum@eduhk.hk
(+852) 29488225
Yen Na Yum
principal investigator · The Education University of Hong Kong

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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