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MoodTECHWISENCT06664944

Technology Exposure and Child Health: Wellness Impact and Social Effects: An Observational Product Registry Study

An observational study of Mood and Depression Disorders, run by Aura at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this study is to understand how children's mobile device usage (smartphones or tablets), including social media use and online games, are related to their mental wellness and mental health, as well as some aspects of their physical activity and sleep. Read more about this study

Who is it for?
Ages 8 to 17 yearsHealthy volunteers can take part
Conditions the study is for
Mood, Depression Disorders, Anxiety Disorders
Type of treatment
Pill or oral medicine
How many people
912 participants
Where
1 siteUnited States
Study dates
15 Nov 2024to 13 Apr 2026
How long will I take part?
3 Months
Phase
Observational
Are there results?
None posted in the registry

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 8 to 17 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: US-based, English-speaking, parents and children who use mobile devices for social media and online games.

Who may be able to join

  • Child participants are male, female, non-binary persons, ages 8-17, inclusive
  • Parent/Authorized Legal Guardian willing to provide informed consent; child willing to provide assent
  • Both Parent/Authorized Legal Guardian and child own a mobile device that already has the Aura app or is able to install and run the Aura app, and the appropriate parental control features.
  • Parent/Authorized Legal Guardian and child are willing for child to use a dedicated device for the duration of the study (ie., child cannot share device with a sibling or other family member).
  • Multiple children from the same family are eligible to participate, provided that each enrolled child uses a dedicated device AND is able to complete outcome assessments independently, AND that parent/authorized legal guardian is able to complete assessments for each enrolled child.
  • Both Parent/Authorized Legal Guardian and child willing to share data collected as part of the Aura app and related device applications
Show all 9Show fewer
  • Consented Parent/Authorized Legal Guardian and child maintain active Aura accounts throughout their study participation
  • Consented Parent/Authorized Legal Guardian and child are able to follow written and verbal instructions (English) as assessed by the PI and/or study coordinator
  • Consented Parent/Authorized Legal Guardian and child are to comply with all testing and study requirements

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Aura

    Boston, Massachusetts, 02210

Other trials in United States

About this study

Official title: Technology Exposure and Child Health: Wellness Impact and Social Effects (TECHWISE): An Observational Product Registry Study

The goal of this study is to understand how children's mobile device usage (smartphones or tablets), including social media use and online games, are related to their mental wellness and mental health, as well as some aspects of their physical activity and sleep. This study is available to all children between the ages of 8 and 17 years and a parent/caregiver.

Researchers will compare participant mobile device usage with their survey responses on sleep, stress, mental health, and physical activity, as well as their parent/caregiver's survey responses.

Read more

Participants will:

  • run the Aura app with parental controls on their dedicated mobile device
  • complete monthly surveys
  • answer daily questions on mood, stress, sleep and physical activity

The study is fully virtual. Duration is 3 months.

Read the detailed description

Once enrolled, child participants will use their mobile devices as usual, and Aura will collect data on on-line and off-line activity, app usage, social interaction, sleep, location and activity levels.

The child participant will complete surveys on a monthly basis, including:

  • A range of questionnaires about feelings and behaviors that are associated with mental health challenges
  • Questionnaires that ask about well-being and positive feelings, including relationships with family and friends
  • Questionnaires that ask about experiences with social media and device usage
  • A questionnaire about feelings of loneliness
  • A questionnaire that asks about activity sleep

In parallel, the parent participant will complete monthly surveys about the child, including:

  • Medical history and changes
  • A range of questionnaires about feelings and behaviors that are associated with mental health challenges
  • Questionnaires that ask about well-being and positive feelings, including relationships with family and friends
Keywords
digital health, digital mental health, technology impacts on mental health, digital natives, digital parenthood, child online safety, digital wellness, child online well-being
Medical subject headings
Anxiety Disorders, Feeding and Eating Disorders, Motor Activity

What participants receive

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

Study groups in NCT06664944
Study groupRoleWhat they receive
Children 8-17 years oldOver 84% of children ages 8 and up have access to a mobile device (smartphone, tablet) and are active on social media. This study focuses on children ages 8-17 to better understand social media usage and how it relates to their mental well-being.

What is being measured

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

  1. Assess ongoing technology use to explore children's online behaviors and derived health behaviors.

    Assess ongoing technology use via the Aura app, including social media and other online behaviors, as well as other smartphone derived health behaviors, such as sleep, location, and activity levels.

    Measured: December 2025

Secondary outcomes (2)
  1. Examine bivariate associations between technology use features and mental wellness and mental health outcomes

    Given the wide range of variables that can be derived from the Aura app, and the number of assessments that will be collected, all analyses should be considered exploratory. As an initial exploration of this objective, we will conduct simple bivariate analyses between technology use variables and mental health outcomes. Example questions include:

    • Are the temporal patterns of device usage (eg., more evening or late-night use) associated with sleep or physical activity outcome measures?
    • Does digital stress mediate the relationship between device usage and mental health outcomes?

    Measured: December 2025

  2. Develop preliminary predictive models that use technology use and smartphone-derived parameters to predict point-in-time mental health outcomes

    Develop preliminary predictive models that use technology use and smartphone-derived parameters to predict point-in-time mental health outcomes, as well as change over time.

    A wide range of analytic techniques will be used to develop and evaluate predictive models to determine whether mental health related outcomes and their change over time can be reliably predicted from device usage data. Example prediction models that may be evaluated but are not limited to the following:

    Do patterns/changes in device-mediated social interactions predict presence/severity of loneliness? Are there specific patterns of keyboard data (specific search terms, text messaging sentiment, etc.) that predict changes in mood or anxiety outcomes? Related, do patterns of keyboard activity map onto daily ratings of mood/stress/anxiety? Can patterns of device usage predict changes in health care utilization over time?

    Measured: December 2025

Timeline

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

  1. First posted30 Oct 2024
  2. Study start15 Nov 2024
  3. Primary completion13 Apr 2026
  4. Study completion13 Apr 2026

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
912 participants (actual)
Target duration
3 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06664944
Sponsor's protocol ID
20243405
Acronym
TECHWISE
Status last verified
Apr 2026
First submitted
28 Oct 2024
Last updated
15 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kollins SH, Flannery J, Goetz K, Akre-Bhide S. Technology Effects and Child Health: Wellness Impact and Social Effects (TECHWISE): Protocol for a Prospective, Observational, Real-World Study. JMIR Res Protoc. 2025 Jun 19;14:e69358. doi: 10.2196/69358.

    PubMed 40424191

Questions about this trial

What is this clinical trial studying?

An observational study of Mood and Depression Disorders, run by Aura at 1 site in United States.

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 9 inclusion and 0 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: finished, as of the sponsor's last update on 15 Apr 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 United States. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assess ongoing technology use to explore children's online behaviors and derived health behaviors. (time frame: December 2025). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06664944, which also lists 1 linked publication.

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 15 Apr 2026.

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