Mobile Behavioral Activation Program With Wearable Sensors and Secure Activity Verification
MBAP-X
A Mobile-Integrated Behavioral Activation Program Using Wearable Sensor Support and Optional Decentralized Data Verification to Enhance Daily Productivity in Healthy Adults
1 other identifier
interventional
227,000
1 country
1
Brief 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 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2026
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 25, 2026
CompletedStudy Start
First participant enrolled
January 25, 2026
CompletedFirst Posted
Study publicly available on registry
February 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 25, 2099
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 25, 2099
February 3, 2026
January 1, 2026
73 years
January 25, 2026
January 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
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.
8 weeks from baseline enrollment
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.
8 Weeks from baseline enrollment
Secondary Outcomes (2)
Change in Self-Reported Daily Productivity
8 weeks from baseline enrollment
Change in Routine Stability Index
8 weeks from baseline enrollment
Study Arms (3)
Experimental - Mobile App Only
EXPERIMENTALParticipants 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.
Experimental - Mobile App + Wearable Sensor
EXPERIMENTALParticipants 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.
Experimental - Mobile App + Wearable Sensor + Secure Activity Verification
EXPERIMENTALParticipants 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.
Interventions
Participants receive daily behavioral activation tasks, structured prompts, and routine-building cues delivered through the mobile app only.
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.
Participants receive behavioral activation tasks, sensor-based feedback, and secure verification of activity logs through a tamper-resistant verification layer.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Truway Health, Inc.
New York, New York, 10016, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gavin Solomon, CEO
Truway Health, Inc.
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 25, 2026
First Posted
February 3, 2026
Study Start
January 25, 2026
Primary Completion (Estimated)
January 25, 2099
Study Completion (Estimated)
January 25, 2099
Last Updated
February 3, 2026
Record last verified: 2026-01