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Health BehaviorMBAP-XNCT07382804

Mobile Behavioral Activation Program With Wearable Sensors and Secure Activity Verification

A study testing Behavioral: Mobile Behavioral Activation App, Mobile App + Wearable Activity Sensor and Mobile App + Wearable Sensor + Secure Activity Verification Layer in people with Health Behavior and Behavioral Activation, run by Truway Health, Inc. at 1 site in United States.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

This study evaluates a mobile-integrated behavioral activation program designed to help adults improve their daily productivity, motivation, and task engagement. The program combines a smartphone application, wearable sensor data, and a decentralized data-verification layer to support participants as they build… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Behavioral: Mobile Behavioral Activation App, Mobile App + Wearable Activity Sensor and Mobile App + Wearable Sensor + Secure Activity Verification Layer
Could I receive a placebo?
No, everyone receives an active treatment
How many people
227,000 participants
Where
1 siteUnited States
Study dates
25 Jan 2026to 25 Jan 2099
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

  • Adults age 18 or older
  • Owns a compatible smartphone capable of running the study app
  • Willing to wear a lightweight activity sensor during waking hours (for applicable arms)
  • Able to read and understand study instructions in English
  • Willing to complete daily tasks and weekly check-ins through the mobile app
  • Provides informed consent

Who cannot join

  • Any condition that would prevent use of a mobile app or wearable sensor (e.g., inability to operate a smartphone)
  • Any condition that would interfere with participation in daily behavioral tasks as determined by the research team
  • Current participation in another digital-behavioral intervention study
  • Inability or unwillingness to comply with study procedures
  • Plans to travel or relocate in a way that would prevent consistent participation during the study period

Trial locations and contacts

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

United States1 site
  • Truway Health, Inc.

    New York, New York, 10016

Other trials in United States

About this study

Official title: A Mobile-Integrated Behavioral Activation Program Using Wearable Sensor Support and Optional Decentralized Data Verification to Enhance Daily Productivity in Healthy Adults

This study evaluates a mobile-integrated behavioral activation program designed to help adults improve their daily productivity, motivation, and task engagement. The program combines a smartphone application, wearable sensor data, and a decentralized data-verification layer to support participants as they build healthier routines and increase consistent daily activity.

Behavioral activation is a well-established psychological approach that encourages individuals to take small, structured actions that align with their goals and values. In this study, participants receive daily prompts, activity suggestions, and personalized behavioral tasks through a mobile app. The app uses information from a wearable sensor-such as movement patterns, activity levels, and environmental cues-to help participants track progress and stay engaged with the program.

Read more

A unique feature of this study is the use of decentralized data verification. Participants' activity logs and task completions are recorded in a secure, tamper-resistant system that allows them to maintain control over their own data while ensuring accuracy and transparency. This approach supports participant autonomy and strengthens the reliability of the study's outcome measures.

The study aims to understand whether combining behavioral activation with real-time sensor feedback and decentralized data verification can improve daily productivity, increase follow-through on planned tasks, and support healthier routines. Participants will use the mobile app and wearable device for the duration of the study and will complete periodic check-ins to share their experiences, challenges, and overall satisfaction with the program.

The research team will evaluate changes in daily activity patterns, task completion rates, self-reported productivity, and engagement with the behavioral activation tasks. Findings from this study may help inform future digital health tools that support motivation, routine-building, and personal productivity in everyday life.

Read the detailed description

Daily functioning in modern environments is often affected by high cognitive load, fragmented attention, and inconsistent routines. Many adults experience difficulty initiating tasks, sustaining engagement, and maintaining productive habits. Behavioral Activation (BA), originally developed for mood-related conditions, provides a structured approach for increasing engagement in meaningful activities and reducing avoidance patterns. BA emphasizes that action precedes motivation and that small, achievable behaviors can create reinforcement cycles that improve daily functioning.

Mobile technology and wearable sensors now allow BA principles to be delivered in real time. Wearable devices can detect movement patterns, activity levels, sleep-related rhythms, and environmental cues. When paired with a mobile application, these data streams support adaptive prompts, personalized task suggestions, and real-time feedback. This integration enables interventions to occur in natural environments rather than relying solely on retrospective self-report.

To enhance transparency and participant autonomy, the study incorporates a decentralized verification layer. Traditional digital-health systems rely on centralized data storage controlled by the research team. In contrast, decentralized verification provides tamper-resistant logs, participant-controlled data review, and transparent audit trails. This approach supports data integrity and participant trust.

The study evaluates a mobile-integrated behavioral activation program supported by wearable sensors and a decentralized verification layer. The objective is to determine whether this combined approach can improve daily functioning, increase follow-through on planned tasks, and support healthier routines in adults seeking to enhance their productivity.

Being tested
Behavioral: Mobile Behavioral Activation App, Mobile App + Wearable Activity Sensor, Mobile App + Wearable Sensor + Secure Activity Verification Layer
Keywords
Daily productivity, Task engagement, Routine building, Motivation, Behavioral patterns, Activity monitoring, Wearable sensor data, Ecological momentary intervention, Digital behavioral tools, Circadian activity patterns, Behavioral reinforcement, Adaptive prompting, Digital phenotyping, Participant-controlled data, Decentralized verification
Medical subject headings
Health Behavior, Sedentary Behavior

What participants receive

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

  • Behavioral: Mobile Behavioral Activation AppBehavioural

    Participants receive daily behavioral activation tasks, structured prompts, and routine-building cues delivered through the mobile app only.

  • Mobile App + Wearable Activity SensorBehavioural

    Participants receive behavioral activation tasks through the mobile app and wear an activity sensor that provides real-time movement data used to tailor prompts and support engagement.

  • Mobile App + Wearable Sensor + Secure Activity Verification LayerBehavioural

    Participants receive behavioral activation tasks, sensor-based feedback, and secure verification of activity logs through a tamper-resistant verification layer.

Study groups in NCT07382804
Study groupRoleWhat they receive
Experimental - Mobile App OnlyExperimentalParticipants use a mobile behavioral activation application that delivers daily tasks, reminders, and routine-building prompts. No wearable sensor or secure activity-verification layer is used in this arm.
Receives: Behavioral: Behavioral: Mobile Behavioral Activation App
Experimental - Mobile App + Wearable SensorExperimentalParticipants use the same mobile behavioral activation app as Arm 1 and also wear a lightweight activity sensor that passively tracks movement and activity patterns. Sensor-derived activity data may inform the timing or intensity of app-delivered prompts.
Receives: Behavioral: Mobile App + Wearable Activity Sensor
Experimental - Mobile App + Wearable Sensor + Secure Activity VerificationExperimentalParticipants use the mobile behavioral activation app and wearable activity sensor. Activity logs are additionally processed through a secure verification layer that provides participant-controlled, tamper-evident activity records used for engagement tracking and outcome analysis.
Receives: Behavioral: Mobile App + Wearable Sensor + Secure Activity Verification Layer

What is being measured

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

  1. Change in Average Daily Active Minutes

    Average number of minutes per day spent in non-sedentary activity, as captured by the wearable activity sensor (for applicable arms) and inferred from app interaction logs (for all arms). Daily active minutes will be averaged over the assessment period and compared across intervention arms to evaluate whether adding a wearable sensor and decentralized verification layer increases real-world physical activation associated with behavioral tasks.

    Measured: 8 weeks from baseline enrollment

  2. Change in Daily Task Completion Rate

    Proportion of assigned behavioral activation tasks completed per day, as recorded by the mobile app, averaged over the assessment period. Daily task completion rate will be compared across intervention arms (mobile app only; mobile app + wearable sensor; mobile app + wearable sensor + decentralized verification layer) to evaluate the effect of each intervention tier on real-world task follow-through and productivity.

    Measured: 8 Weeks from baseline enrollment

Secondary outcomes (2)
  1. Change in Self-Reported Daily Productivity

    Change in participants' self-reported daily productivity, measured using a brief in-app rating scale (e.g., 0-10) completed at least once per week. Scores will be averaged over the assessment period and compared across intervention arms to assess whether the different intervention tiers (mobile app only; mobile app + wearable sensor; mobile app + wearable sensor + decentralized verification layer) are associated with greater perceived productivity and task effectiveness in daily life.

    Measured: 8 weeks from baseline enrollment

  2. Change in Routine Stability Index

    Change in routine stability, defined as the consistency of daily task timing and completion patterns over the assessment period. Routine stability will be quantified using variability in task completion times and day-to-day fluctuations in task completion rate, derived from app logs (and sensor timestamps where applicable). Lower variability indicates more stable routines. Outcomes will be compared across intervention arms to assess whether adding a wearable sensor and decentralized verification layer supports more consistent daily routines.

    Measured: 8 weeks from baseline enrollment

Timeline

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

  1. First posted3 Feb 2026
  2. Study start25 Jan 2026
  3. Primary completion25 Jan 2099 (estimated)
  4. Study completion25 Jan 2099 (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
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants are assigned to one of several intervention groups operating in parallel. Each group receives a distinct combination of behavioral activation tools: Group A: Mobile app only Group B: Mobile app + wearable activity sensor Group C: Mobile app + wearable sensor + decentralized data verification layer There is no crossover between groups. Each participant engages with their assigned intervention throughout the study period. This design allows for comparative analysis of engagement, productivity, and behavioral outcomes across intervention tiers.
Masking
None (open label)
Enrolment
227,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07382804
Sponsor's protocol ID
TH-MBAP-2026-001
Acronym
MBAP-X
Status last verified
Jan 2026
First submitted
25 Jan 2026
Last updated
3 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Behavioral: Mobile Behavioral Activation App, Mobile App + Wearable Activity Sensor and Mobile App + Wearable Sensor + Secure Activity Verification Layer in people with Health Behavior and Behavioral Activation, run by Truway Health, Inc. 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 6 inclusion and 5 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: enrolling by invitation, as of the sponsor's last update on 3 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?

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?

Change in Average Daily Active Minutes (time frame: 8 weeks from baseline enrollment). The study lists 2 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 3 Feb 2026.

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