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Clinical Trials in the USA / NCT07382804
Enrolling by invitation Not applicable

Mobile Behavioral Activation Program With Wearable Sensors and Secure Activity Verification

NCT07382804 · tracked via the Priya Life Science USA tracker
Sponsor
Truway Health, Inc.
Phase
Not applicable
Started
2026-01-25
Last updated
2026-02-03

Condition(s) studied

Health BehaviorBehavioral ActivationSedentary Behavior

Investigational drug(s) / intervention(s)

Behavioral: Mobile Behavioral Activation AppMobile App + Wearable Activity SensorMobile App + Wearable Sensor + Secure Activity Verification Layer

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

Mobile App + Wearable Activity Sensor: 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 Layer: Participants receive behavioral activation tasks, sensor-based feedback, and secure verification of activity logs through a tamper-resistant verification layer.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Truway Health, Inc. New York New York

More Truway Health, Inc. trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07382804 on ClinicalTrials.gov ↗ ← All trials in the USA