Mobile Behavioral Activation Program With Wearable Sensors and Secure Activity Verification (MBAP-X)

January 30, 2026 updated by: Truway Health, Inc.

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.

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.

Study Overview

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.

Study Type

Interventional

Enrollment (Estimated)

227000

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 Locations

    • New York
      • New York, New York, United States, 10016
        • Truway Health, Inc.

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental - Mobile App Only
Participants 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.
Participants receive daily behavioral activation tasks, structured prompts, and routine-building cues delivered through the mobile app only.
Experimental: Experimental - Mobile App + Wearable Sensor
Participants 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.
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.
Experimental: Experimental - Mobile App + Wearable Sensor + Secure Activity Verification
Participants 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.
Participants receive behavioral activation tasks, sensor-based feedback, and secure verification of activity logs through a tamper-resistant verification layer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Average Daily Active Minutes
Time Frame: 8 weeks from baseline enrollment
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.
8 weeks from baseline enrollment
Change in Daily Task Completion Rate
Time Frame: 8 Weeks from baseline enrollment
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.
8 Weeks from baseline enrollment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Self-Reported Daily Productivity
Time Frame: 8 weeks from baseline enrollment
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.
8 weeks from baseline enrollment
Change in Routine Stability Index
Time Frame: 8 weeks from baseline enrollment
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.
8 weeks from baseline enrollment

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Gavin Solomon, CEO, Truway Health, Inc.

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)

January 25, 2026

Primary Completion (Estimated)

January 25, 2099

Study Completion (Estimated)

January 25, 2099

Study Registration Dates

First Submitted

January 25, 2026

First Submitted That Met QC Criteria

January 30, 2026

First Posted (Actual)

February 3, 2026

Study Record Updates

Last Update Posted (Actual)

February 3, 2026

Last Update Submitted That Met QC Criteria

January 30, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

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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