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PTSD - Post Traumatic Stress DisorderNCT06993012

An Integrative, Digital Health Approach to Veteran-Centered PTSD Care

A study testing Mobile Health Stress Self Management System and Intensive Cycling Activity in people with PTSD - Post Traumatic Stress Disorder and Depression/Anxiety, run by Texas A&M University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this study is to test the effectiveness of a stress self-management mobile health system (smartphone app + wearable sensor) alongside an intense physical cycling intervention to reduce symptoms of stress in a veteran population. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Mobile Health Stress Self Management System and Intensive Cycling Activity
Could I receive a placebo?
No, everyone receives an active treatment
How many people
37 participants
Where
1 siteUnited States
Study dates
21 Apr 2025to 1 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

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 aged 18 and older
  • Self-identifies as Veteran
  • Participant has reliable internet access for their phone (Either WIFI or mobile data plan)
  • Own an iPhone (IOS 13 or newer)
  • score >10 on the PCL-5 test
  • Additionally, participants to be assigned to either intervention group must have registered for a Project Hero Ride 2 Recovery event.

Who cannot join

  • people unable to consent
  • pregnant women where the activities of the research may affect the pregnancy or the fetus
  • minors under 18 years of age
  • prisoners

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Texas A&M University

    College Station, Texas, 77843

Other trials in United States

About this study

The goal of this study is to test the effectiveness of a stress self-management mobile health system (smartphone app + wearable sensor) alongside an intense physical cycling intervention to reduce symptoms of stress in a veteran population. The main questions this study aims to answer are:

Does a mobile stress self-management system alongside intensive physical activity reduce the amount of physiologically detected, via machine-learning algorithm, stressful moments or PTSD hyperarousals?

Read more

Can a mobile stress self-management system alongside intensive physical activity reduce symptoms of stress, anxiety, and depression on self-assessments like PCL-5, GAD-7, and PHQ-8?

Participants will:

Use a stress self-management system called First Watch Device (FWD) and confirm/deny detected stress moments on the app for a 2 month period.

Use FWD self-management features as coping stragies for mental health and stressors for a 2 month period.

Participate in the Project Hero 1-week Ride 2 Recovery Challenge events in the middle of the study.

Read the detailed description

Setting of the study: Data will be collected from participants recruited from bike riding events hosted by collaborator Project Hero. Their rides include participants from across the U.S., but specific riding challenges will take place in major areas such as Texas, California, the Great Lakes region, and Nevada in the year 2025 onward. The same study procedure will occur at each location. The participants will also participate in the study from their home locations.

Study design: The investigators propose a single-blind three-group randomized controlled trial comparing: (1) a digital health self-management intervention combined with an intensive group-based physical activity intervention, (2) an intensive group-based physical activity intervention without the digital health component (active comparator), and (3) a no-intervention control group. Mental health symptomatology will be measured across three time intervals to assess within-subject effects over a two-month period: pre-intervention (one month), during the intervention (one week), and post- intervention (one month). Participants in the experimental groups will be recruited from veteran registrants of the Project Hero Ride 2 Recovery 7-day Texas challenge (and 7-day California challenge or 10-day Europe challenge, based on registration numbers), while the participants for the control group will be selected from the broader Project Hero veteran community not registered for the Ride 2 Recovery events. Participants in the two intervention groups will be randomly placed into their groups using an RStudio randomization script. Participants in the control group will be selected from members of the veteran community that are not participating in the Ride 2 Recovery events of their own volition.

All participants will wear an Apple Watch and download the FWD app for the duration of the study to measure stress moments (via machine learning model with heart rate and accelerometer data as inputs) and take psychological assessment surveys (GAD-7, PHQ-9, and PCL-5). Participants in the control group will not have access to the app features aside from tracking heart rate, stress moments, and psychological assessments. Participants in the control group and physical intervention group without digital intervention will still be asked to perform weekly self-assessments of mental health conditions as well as self-report stress moments and respond to app-detected stress moments to validate the ML algorithm. Participants in the digital intervention group will have full access to the First Watch Device app (FWD), which includes a wide suite of self-management material such as relaxation techniques, links to outside resources, educational material, emergency SOS messages to contacts, and monitoring of symptoms. One on one interviews may be performed with the participants at the start of each phase of the study: pre-intervention, during intervention, and post-intervention as well as a follow up at the end of the post-intervention period where they will be asked about their experience with the interventions, managing their symptoms, and the usability of the FWD app. At the end of the study, both versions of the FWD app (control and digital intervention) will be made available to participants at their request until app usage expires.

This study combines Project Hero's Ride 2 Recovery, an intensive group-based cycling intervention, with a digital health self-management tool to enhance PTSD symptom monitoring and support. Each Ride 2 Recovery event is performed in a different location. The events of interest for this study are the 1 week long rides that take place in Texas (in Spring) and California (in Fall) once a year. Participants in the ride generally ride for most of the day (6-8 hours) across a predetermined route within the state. Eligible participants are veterans and first responders. The digital intervention leverages Apple smartwatches to (1) Continuously monitor key physiological indicators (e.g., HRV, skin temperature, electrodermal activity) for early distress detection; and (2) Deliver real-time, personalized interventions via the Mental Health Evaluation and Lookout Program (mHELP) bundle, offering symptom tracking, self-management tools, and access to counseling. Access to counseling is provided through the "Link" navigation screen on the app, which provides several contacts for veteran crisis lines, hotlines, call centers, and the Veterans Health Administration. Using advanced ML algorithms, the system will identify and examine physiological data to trigger timely alerts and tailored recommendations. For example, when FWD detects a hyperarousal event, akin to a panic attack, the app will prompt the user to open the app and perform relaxation mechanisms like breathing and also allow the user to send an SOS message to their emergency contacts by tapping on their watch. Additionally, user notifications are programmed into the app to remind users to review educational material as well as complete psychological surveys. A suite of self-management tools is provided for on-demand and recommended access, including breathing and focusing exercises, relaxing media, multimodal educational material, journaling tools, trends and visualizations of mental health status, mental health self-assessment, and more. The tool will also enable self-reports of hyperarousal events (double tapping on the watch interface or using an accessible feature on the mobile app). The integration of smartwatch technology with physical activity aims to provide scalable, accessible, and personalized support for veterans, enhancing their mental health and overall resilience.

Data Collection: To assess the impact of the interventions on mental health symptoms, both subjective and objective data will be collected via Apple Watch and smartphone. Subjective measures will be gathered at four time points-one month before the Texas Challenge event (or at any number of recurring Challenge events thereafter depending on award date and registrant numbers), pre-event, post-event, and one month after the event-to evaluate participants' perceived mental health status and track changes over time. Psychological well-being will be assessed using validated self-report instruments, including: (i) the PTSD Checklist for DSM-5 (PCL-5) to measure PTSD symptom severity (Aim 1); (ii) the Patient Health Questionnaire (PHQ-9) to assess depression symptom severity (Aim 2); and (iii) the Generalized Anxiety Disorder 7-item (GAD-7) scale to evaluate symptom severity of generalized anxiety (Aim 2). These surveys will be programmed within the FWD app, which will act as a central hub for these participants during the course of the study. Notifications from the app will be sent to the participants on their phones to complete these if not done on a timely manner. These measures will provide valuable insights into the differential effects of the interventions on participants' mental health. As objective measures, physiological data, which include heart rate measured in beats per minute and accelerometer data, will be collected one month before, during, and one month after the Texas Challenge event via Apple Watch (Aim 3). The event will provide a dynamic environment to observe fluctuations in physiological measures under real-world conditions. Participants will wear an Apple Watch throughout the study to continuously monitor heart rate (BPM), accelerometer data, and subjective stress ratings. This timeline will allow for a comprehensive analysis of physiological changes over time, with a focus on responses to potential PTSD triggers during high-intensity activities such as long-distance cycling.

Data analytics: The data will be analyzed using Generalized Linear Mixed Modeling (GLMM) to evaluate the impact of interventions on mental health symptomatology over time (pre-during-and-post event phases). GLMM is appropriate for this study as it accommodates the hierarchical structure of repeated measurements nested within individuals and individuals nested within groups. This approach allows for the inclusion of both fixed effects (e.g., intervention type, time points) and random effects (e.g., individual variability), providing a flexible framework for modeling complex data. GLMM is particularly advantageous for a longitudinal design as it handles repeated measures data, accounts for correlations among observations, and allows for non-normal outcome distributions. GLMM can also incorporate random intercepts and slopes to capture individual variability, tolerate missing data, and model interaction effects. This analysis will focus on the fixed effects of intervention type and time, as well as their interaction, to determine the efficacy of the digital health intervention, with simple slope and pairwise contrast analyses to examine time and group differences.

Being tested
Mobile Health Stress Self Management System, Intensive Cycling Activity
Keywords
mobile health, veterans, ptsd, wearable sensor, machine-learning, stress self-management
Medical subject headings
Combat Disorders, Depression, Anxiety Disorders, Stress Disorders, Post-Traumatic

What participants receive

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

  • Mobile Health Stress Self Management SystemBehavioural

    FWD has been developed using proprietary machine-learning algorithms to detect physiological markers of stress/PTSD hyperarousal in veterans using a wearable smart watch sensor. Additionally, FWD includes a suite of self-management and monitoring tools through the smartphone app designed through several rounds of human factors design

  • Intensive Cycling ActivityBehavioural

    The Project Hero Ride 2 Recovery is a unique event hosted by Project Hero where veterans participate in a week long cycling challenge where they cycle across the continental US about 50-70 miles per day for a total of over 350 miles within a group of peers.

Study groups in NCT06993012
Study groupRoleWhat they receive
Digital intevention + physical interventionExperimentalThis group will receive full access to FWD and participate in the 1-week intensive cycling intervention.
Receives: Behavioral: Mobile Health Stress Self Management System; Behavioral: Intensive Cycling Activity
Physical intervention onlyActive comparatorThis group will have a control version of FWD and participate in the intensive cycling intervention.
Receives: Behavioral: Intensive Cycling Activity
No interventionNo interventionThis group will have a control version of FWD and not participate in the intensive cycling intervention.

What is being measured

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

  1. ML-detected Stress Moments

    Stress Moments is a conceptual real-time measure derived from a combination of physiological heart rate (heartbeats per minute - bpm) measurements and subjective self-reports, both collected through the FWD application on the Apple Watch. Continuous HR data were recorded using either the Apple Watch Series 4 or 5, measuring bpm at a frequency of 1 Hz, enabling high-resolution monitoring for precise identification of physiological stress indicators. Stress events were detected using an integrated algorithm analyzing HR fluctuations, and these were automatically logged in the dataset under a designated "stress detection" column.

    Measured: From enrollment through completion of the study, an average of 10 weeks

Secondary outcomes (3)
  1. PCL-5 Score

    Self-reported validated measure for stress/PTSD on the PCL-5 scale.

    Measured: Weekly through study completion, an average of 10 weeks

  2. GAD-7 Score

    Self-reported validated measure for anxiety on the GAD-7 scale.

    Measured: Weekly through study completion, an average of 10 weeks

  3. PHQ-8 Score

    Self-reported validated measure for depression on the PHQ-8 scale.

    Measured: Weekly through study completion, an average of 10 weeks

Timeline

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

  1. First posted28 May 2025
  2. Study start21 Apr 2025
  3. Primary completion6 Jun 2026
  4. Study completion1 Jul 2026

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
One group will receive full access to FWD and participate in the 1-week intensive cycling intervention. One group will have a control version of FWD and participate in the intensive cycling intervention. One group will have a control version of FWD and not participate in the intensive cycling intervention.
Masking
None (open label)
Enrolment
37 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06993012
Sponsor's protocol ID
STUDY2025-0124
Status last verified
Aug 2026
First submitted
13 May 2025
Last updated
27 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD will not be shared in this study as we plan to keep the personalized data private within the research personnel on the approved protocol. Rather, aggregate data will be published via journal article.

Questions about this trial

What is this clinical trial studying?

A study testing Mobile Health Stress Self Management System and Intensive Cycling Activity in people with PTSD - Post Traumatic Stress Disorder and Depression/Anxiety, run by Texas A&M University 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 4 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: finished, as of the sponsor's last update on 27 Aug 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

ML-detected Stress Moments (time frame: From enrollment through completion of the study, an average of 10 weeks). 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 27 Aug 2026.

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