A Randomized Controlled Ecological Momentary Intervention to Improve Digital Self-Regulation and Well-Being

March 30, 2026 updated by: The Hong Kong Polytechnic University

Activating Metacognition in Daily Life: A Randomized Controlled Ecological Momentary Intervention to Improve Digital Self-Regulation and Well-Being

The primary objective of this study is to examine whether an ecological momentary intervention (EMI), combining behavioral self-monitoring (screen time screenshot uploads) and structured reflection, can enhance metacognitive awareness and metacognitive regulation in the context of recreational screen time among young adults.

A secondary objective is to investigate whether improvements in metacognitive processes are associated with subsequent changes in behavioral and psychological outcomes, including recreational screen time (RST), stress, and life satisfaction.

Furthermore, this study aims to elucidate the underlying mechanisms through which the intervention exerts its effects by integrating a randomized controlled trial (RCT) design with intensive longitudinal (daily diary) data.

Specifically, the study addresses the following research questions:

RQ1 (Primary Intervention Effect on Metacognition): Does the EMI lead to higher levels of daily metacognitive awareness and metacognitive regulation (planning, monitoring, and evaluation) compared to the control group? RQ2 (Within-person Associations): At the within-person level, do day-to-day fluctuations in metacognitive awareness and regulation predict same-day and next-day changes in recreational screen time, stress, and life satisfaction? RQ3 (Mediating Mechanism): Do increases in metacognitive awareness and regulation mediate the effects of the EMI on recreational screen time, stress, and life satisfaction? RQ4 (Between-person Effects): At the between-person level, do individuals in the intervention group exhibit higher average levels of metacognitive awareness and regulation, as well as lower recreational screen time and stress and higher life satisfaction, compared to those in the control group?

Study Overview

Study Type

Interventional

Enrollment (Estimated)

240

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 Contact

Study Locations

    • Select An Option…
      • Hong Kong, Select An Option…, Hong Kong
        • Recruiting
        • The Hong Kong Polythechnic University
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Participants must meet all of the following criteria:

  1. Age between 18 and 25 years old.
  2. Own and regularly use a smartphone.
  3. Report an average daily recreational screen time of at least 3 hours on weekdays or 4 hours on weekends, based on self-report (Zablotsky et al., 2025).
  4. Be able to access their device's built-in screen time tracking function (or equivalent system-level usage report) and upload screenshots when required.
  5. Be willing and able to complete daily surveys throughout the full study period.
  6. Indicate motivation to reduce or regulate their recreational screen use.

Exclusion Criteria:

  1. Outside the age range of 18-25 years.
  2. Do not own a smartphone or do not use it regularly.
  3. Report average daily recreational screen time below 3 hours on weekdays and below 4 hours on weekends.
  4. Are unable to access device-based screen time tracking functions or cannot provide valid screenshots when required.
  5. Are unwilling or unable to complete daily surveys across the study period (e.g., anticipated non-compliance, scheduling constraints).
  6. Do not express motivation to reduce or regulate their recreational screen use.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Ecological Momentary Intervention Group

Participants in the intervention group will receive a composite ecological momentary intervention that integrates behavioral self-monitoring and metacognitive reflection.

Specifically, each day participants will:

  1. Upload a screenshot of their device-recorded screen time (e.g., iOS Screen Time or Android Digital Wellbeing), serving as a form of behavioral self-monitoring.
  2. Complete structured reflection prompts designed to activate metacognitive processes, including reflection on:

(1) total recreational screen time, (2) usage contexts (e.g., situations or triggers), (3) awareness of potential overuse, and (4) use of regulation strategies (e.g., planning, monitoring, evaluation). In addition, participants will complete daily measures of metacognitive awareness, metacognitive regulation, stress, and life satisfaction.

A composite ecological momentary intervention that integrates behavioral self-monitoring and metacognitive reflection.

Specifically, each day participants will:

  1. Upload a screenshot of their device-recorded screen time (e.g., iOS Screen Time or Android Digital Wellbeing), serving as a form of behavioral self-monitoring.
  2. Complete structured reflection prompts designed to activate metacognitive processes, including reflection on:

(1) total recreational screen time, (2) usage contexts (e.g., situations or triggers), (3) awareness of potential overuse, and (4) use of regulation strategies (e.g., planning, monitoring, evaluation).

No Intervention: Control Group
Participants in the control group will complete the same daily diary measures of metacognitive awareness, metacognitive regulation, stress, and life satisfaction, but will not engage in screen time self-monitoring (i.e., no screenshot uploads) and will not receive any structured reflection prompts.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Daily Metacognitive Awareness
Time Frame: 14-day dairy
Daily Metacognitive Awareness assesses the extent to which participants were consciously aware of their motivations and tendencies regarding recreational screen use on that day, which adapted from metacognitive awareness dimension in Metacognition about Regulating Recreational Screen Time Scale (McRST). Sample items include: "Today, I was aware of why I wanted to use my device for recreational purposes." Items are rated on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). Higher scores indicate greater daily metacognitive awareness.
14-day dairy
Daily Recreational Screen Time
Time Frame: 14-day dairy
Daily Recreational Screen Time is assessed using both subjective self-reports and objective device-recorded data in order to enhance measurement validity and reduce recall bias. Recreational screen time is defined as non-work and non-study device use, including activities such as social media browsing, video streaming, gaming, and other entertainment-related engagement.
14-day dairy
Metacognitive skills
Time Frame: baseline, day 15 (t1)
Metacognitive skills will be assessed using the Metacognition about Regulating Recreational Screen Time Scale (Mc-RST). The scale captures individuals' knowledge, beliefs, and perceived efficacy regarding their ability to regulate recreational screen use. Participants rated on a 5-point Likert scale, with higher scores indicating stronger metacognitive awareness and perceived regulatory capacity.
baseline, day 15 (t1)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Daily Stress
Time Frame: 14-day dairy
Daily Stress is assessed using brief items adapted to capture day-specific perceived stress. Participants indicate the extent to which statements such as "Today, I felt stressed," "Today, I felt overwhelmed," and "Today, I found it difficult to cope with daily demands" describe their experience. Responses are rated on a 5-point scale ranging from 1 (not at all) to 5 (very much), with higher scores indicating greater daily stress.
14-day dairy
Daily Life Satisfaction
Time Frame: 14-day dairy
Daily Life Satisfaction captures participants' cognitive evaluation of their day. Participants respond to items such as "Overall, I was satisfied with today," "Today was close to my ideal day," and "I feel positive about how today went." Responses are rated on a 5-point scale ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores indicate greater daily life satisfaction.
14-day dairy
Internet addiction
Time Frame: baseline, day 15 (t1)
Internet addiction will be measured using the revised Chinese Internet Addiction Scale (CIAS-R; Bai & Fan, 2005), which assesses core symptoms and related problems of excessive Internet use, including compulsive use, withdrawal, tolerance, interpersonal difficulties, and time management issues. Participants responded to items based on their experiences over the past year using a 4-point scale, with higher scores indicating greater levels of problematic Internet use.
baseline, day 15 (t1)
Short-form video addiction
Time Frame: baseline; day 15(t1)
Short-form video addiction will be assessed using the Bergen Short Video Addiction Scale (Qu et al., 2024), which captures key components of addictive behavior, including salience, mood modification, tolerance, withdrawal, conflict, and relapse. Items were rated on a 5-point frequency scale, with higher scores indicating more severe short-form video addiction.
baseline; day 15(t1)
Depressive symptoms
Time Frame: baseline; day 15(t1)
Depressive symptoms will be measured using the Patient Health Questionnaire-9 (PHQ-9; Leung et al., 2020), which assesses the frequency of depressive symptoms over the past two weeks. Each item was rated on a 4-point scale, with higher total scores indicating more severe depressive symptoms.
baseline; day 15(t1)
Anxiety symptoms
Time Frame: baseline; day 15(t1)
Anxiety symptoms will be assessed using the Generalized Anxiety Disorder-7 scale (GAD-7; He et al., 2010), which evaluates the frequency of anxiety-related symptoms over the past two weeks. Items were rated on a 4-point scale, with higher scores indicating higher levels of anxiety.
baseline; day 15(t1)
Perceived stress
Time Frame: baseline; day 15(t1)
Perceived stress will be measured using the Chinese version of the Perceived Stress Scale (CPSS; Yang & Huang, 2003), which assesses the extent to which individuals perceive their lives as unpredictable, uncontrollable, and overloaded. Participants rated items on a 5-point scale, with higher scores indicating higher perceived stress.
baseline; day 15(t1)
Self-control
Time Frame: baseline; day 15(t1)
Self-control will be assessed using the Chinese version of the Self-Control Scale (SCS; Unger et al., 2016), which measures individuals' ability to regulate impulses and maintain goal-directed behavior. Items were rated on a 6-point scale, and higher average scores indicate stronger self-control capacity.
baseline; day 15(t1)
Life satisfaction
Time Frame: baseline; day 15(t1)
Life satisfaction will be measured using the Satisfaction with Life Scale (SWLS; Diener et al., 1985), which assesses global cognitive judgments of one's life satisfaction. Participants rated five items on a 7-point Likert scale, with higher scores indicating greater life satisfaction.
baseline; day 15(t1)
Fear of missing out (FoMO)
Time Frame: baseline; day 15(t1)
Fear of missing out (FoMO) will be assessed using a validated FoMO scale (Przybylski et al., 2013; Li et al., 2019), which captures individuals' anxiety related to missing rewarding experiences or social interactions. Items were rated on a 5-point scale, with higher scores indicating higher levels of FoMO.
baseline; day 15(t1)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

March 1, 2026

Primary Completion (Estimated)

May 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

March 30, 2026

First Submitted That Met QC Criteria

March 30, 2026

First Posted (Actual)

April 6, 2026

Study Record Updates

Last Update Posted (Actual)

April 6, 2026

Last Update Submitted That Met QC Criteria

March 30, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HSEARS20241210004-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data (IPD) will not be publicly shared due to the sensitive nature of the data, which includes detailed daily behavioral records and potentially identifiable digital usage patterns. Although all data will be de-identified, the granularity of longitudinal diary data and screen time records may still pose a risk of re-identification. In addition, data sharing is restricted by institutional ethical approval and participant consent agreements, which limit the use of the data to the current research purposes only. Aggregated data and study materials can be made available upon reasonable request.

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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