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Chronotypes and HealthNot RequiredNCT07410585

Testing the Effectiveness of an Intervention That Aligns Circadian Rhythm With Daily Activities on Student Flourishing

A study testing Use of Owaves App in people with Chronotypes and Health, run by University of California, San Diego at 1 site in United States.

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

Previous studies have examined whether circadian rhythm tracking improves well-being, with some evidence suggesting that aligning daily activities with one's natural chronotype (a person's natural preference for being alert and sleep), enhances well-being and productivity. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Chronotypes and Health
What is being tested?
Use of Owaves App
Could I receive a placebo?
No, everyone receives an active treatment
How many people
400 participants
Where
1 siteUnited States
Study dates
5 Jan 2026to 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 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Currently an undergraduate students from University of California, San Diego (UCSD)
  • Age 18 or older
  • has access to a device to answer Qualtrics questions
  • has access to a device that can download the MyBodyClock App (Apple iPhone or Apple iPad)

Who cannot join

  • Participants who are under the age of 18, are not undergraduate students at UCSD, or do not have access to the Qualtrics question platform and/or the MyBodyClock App

Trial locations and contacts

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

Karen Dobkins, PhD contact

16198468152

KDOBKINS@UCSD.EDU

United States1 site, 1 recruiting
  • UC San Diego

    La Jolla, California, 92037

    Karen Dobkins, PhD, 6198468152, KDOBKINS@UCSD.EDU

    Recruiting

Other trials in United States

About this study

Previous studies have examined whether circadian rhythm tracking improves well-being, with some evidence suggesting that aligning daily activities with one's natural chronotype (a person's natural preference for being alert and sleep), enhances well-being and productivity. However, the current research lacks intervention-based designs like real-time tracking or behavioral alignment tools. Here, the investigators aim to investigate if an active intervention, involving the usage of an app tracking circadian rhythms and making recommendations based on one's circadian rhythm over seven weeks, improves students' flourishing.

Read the detailed description

The aim of this clinical study is to test the effectiveness of an intervention (through an app called Owaves: MyBodyClock that will be provided free of cost) designed to help students align daily activities in accordance with their circadian rhythm. The questions include:

  1. Does the intervention improve both trait and state measures of student flourishing, including general well-being (i.e., happiness), focus, and energy levels?
  2. Does the intervention alter the types of activities participants engage in?
  3. Does the intervention impact the likelihood of seeking resources for physical and mental health?
Being tested
Use of Owaves App

What participants receive

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

  • Use of Owaves AppBehavioural

    Students use the Owaves app for 7 weeks and psychological measures are obatined pre and post to determine the effectiveness of the App

Study groups in NCT07410585
Study groupRoleWhat they receive
Intervention Group who uses OWAVES App for 7 weeksExperimentalIntervention Group who uses OWAVES App for 7 weeks
Receives: Behavioral: Use of Owaves App
Control group who does not use the OWAVES appNo interventionNot described

What is being measured

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

  1. Trait Happiness (Subjective Happiness Scale)

    Subjective Happiness Scale (SHS) Trait questionnaire. The SHS is a 4-item scale of global subjective happiness. It is scored on a 7-point Likert scale where 1 = less happy to 7 = more happy. Total scores range from 4 to 28 where higher scores indicate greater subjective happiness.

    Measured: Baseline (Weeks 1/2) and Weeks 8/9.

  2. Focus Trait (Barkley Adult ADHD Rating Scale (Inattention Subscale) and Academic Time Management and Procrastination Measure)

    The Barkley Adult ADHD Rating Scale is a self-report questionnaire with 18-items which rates the frequency of ADHD symptoms and behaviors. Each item is scored on a 4-point scale ranging from 1 = never or rarely, to 4 = very often. A lower score indicates less severe ADHD symptoms and behaviors.

    Measured: Baseline (Weeks 1/2) and Weeks 8/9.

  3. Energy Trait (Subjective Vitality Scale)

    Subjective Vitality Scale (SVS) is a 6 - item self-report questionnaire to measure the subjective vitality of a participant. It is scored on a 7-point Likert scale where 1 = completely disagree to 7 = completely agree. Higher scores indicates higher level of subjective vitality.

    Measured: Baseline (Weeks 1/2) and Weeks 8/9.

  4. Mindfulness Trait (Five Facet Mindfulness Questionnaire (FFMQ))

    The Five Facet Mindfulness Questionnaire (FFMQ) short form is a 24-item questionnaire that measures mindfulness in participants. Items are scored on a 5-point Likert-type scale ranging from 1 = never/very rarely true to 5 = very often/always true. Higher scores indicate greater levels of mindfulness.

    Measured: Baseline (Weeks 1/2) and Weeks 8/9.

Secondary outcomes (1)
  1. States

    State measures will be obtained within three days of the trait assessments (also in weeks 1/2 and 8/9) using the Daily Reconstruction Method (DRM), in which participants are asked to reconstruct their previous day into episodes and retrospectively report on state variables during each episode (see Raynes \& Dobkins, 2025). The state measures will match the trait measures and ask about:

    • Happiness (State)
    • Focus (State)
    • Energy (State)
    • Mindfulness (State)

    Measured: 7 weeks

Timeline

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

  1. First posted13 Feb 2026
  2. Study start5 Jan 2026
  3. Primary completion31 May 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
Single blind
Who is masked
Participant
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07410585
Sponsor's protocol ID
IRB: #813010
Acronym
Not Required
Status last verified
Feb 2026
First submitted
16 Jan 2026
Last updated
13 Feb 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 Use of Owaves App in people with Chronotypes and Health, run by University of California, San Diego 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 4 inclusion and 1 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 13 Feb 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?

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 Karen Dobkins, PhD (16198468152, KDOBKINS@UCSD.EDU), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Trait Happiness (Subjective Happiness Scale) (time frame: Baseline (Weeks 1/2) and Weeks 8/9.). The study lists 4 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 13 Feb 2026.

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