Collaborating Investigators:
Dr. David Wetter, University of Utah
Funding Status:
NIH/NCI
7/1/15 – 6/30/21
Associated with:
SMARTLife Utah is a three-phase Sequential Multiple Assignment Randomized Trial (SMART) designed to increase the reach and engagement of digital evidence-based interventions (EBIs) for obesity in populations disproportionately affected by limited healthcare access and economic barriers, served by 38 community health center clinics. Obesity, a major risk factor for multiple cancers, exceedingly impacts these populations and contributes to cancer inequities. Despite proven effectiveness, EBIs remain underutilized due to barriers in access and engagement. SMARTLife Utah uses multilevel implementation strategies, including enhanced health information technology (HIT) at the clinic level and telehealth-supported patient navigation, to overcome these barriers. The mDOT Center contributes by integrating its mobile health technology, real-time behavioral monitoring, and AI-driven personalized intervention capabilities to optimize patient engagement and intervention delivery. This partnership advances precision public health by leveraging scalable, technology-enabled solutions embedded within real-world clinical settings to reduce obesity-related disparities and improve cancer prevention.
TR&D1 supports SMARTLife Utah by deploying wearable sensors and smartphone-based assessments to capture real-time data on physical activity, diet, and intervention adherence. Using its expertise in AI-driven digital phenotyping and multimodal data fusion, the Center develops personalized behavioral micromarkers to monitor engagement and response to digital EBIs. It implements real-time monitoring and feedback to identify low adherence or risk behaviors and deliver tailored prompts. The Center also integrates its data platforms with existing health IT systems in community health centers to streamline clinical workflows. Additionally, the mDOT Center provides data analytics, visualization tools, and technical training to support implementation and maximize intervention reach among marginalized populations.
ACM on Interactive, Mobile, Wearable, and Ubiquitous Technologies (IMWUT)
September 7, 2022
behavioral intervention, human-centered computing, risk prediction, smoking cessation, ubiquitous and mobile computing design and evaluation methods, wearable sensors
Passive detection of risk factors (that may influence unhealthy or adverse behaviors) via wearable and mobile sensors has created new opportunities to improve the effectiveness of behavioral interventions. A key goal is to find opportune moments for intervention by passively detecting rising risk of an imminent adverse behavior. But, it has been difficult due to substantial noise in the data collected by sensors in the natural environment and a lack of reliable label assignment of low- and high-risk states to the continuous stream of sensor data. In this paper, we propose an event-based encoding of sensor data to reduce the effect of noises and then present an approach to efficiently model the historical influence of recent and past sensor-derived contexts on the likelihood of an adverse behavior. Next, to circumvent the lack of any confirmed negative labels (i.e., time periods with no high-risk moment), and only a few positive labels (i.e., detected adverse behavior), we propose a new loss function. We use 1,012 days of sensor and self-report data collected from 92 participants in a smoking cessation field study to train deep learning models to produce a continuous risk estimate for the likelihood of an impending smoking lapse. The risk dynamics produced by the model show that risk peaks an average of 44 minutes before a lapse. Simulations on field study data show that using our model can create intervention opportunities for 85% of lapses with 5.5 interventions per day.
We present a model for identifying ideal moments for intervention by passively detecting risk of an imminent adverse behavior.
Sy-Miin Chow, Inbal Nahum-Shani, Justin Baker, Donna Spruijt-Metz, Nicholas Allen, Randy Auerbach, Genevieve Dunton, Naomi Friedman, Stephen Intille, Predrag Klasnja, Benjamin Marlin, Matthew Nock, Scott Rauch, Misha Pavel, Scott Vrieze, David Wetter, Evan Kleiman, Timothy Brick, Heather Perry, Dana Wolff-Hughes
Translational Behavioral Medicine, Volume 13, Issue 1, January 2023, Pages 7–16
November 23, 2022
EMA, health behavior changes, ILHBN, location, sensor
The ILHBN is funded by the National Institutes of Health to collaboratively study the interactive dynamics of behavior, health, and the environment using Intensive Longitudinal Data (ILD) to (a) understand and intervene on behavior and health and (b) develop new analytic methods to innovate behavioral theories and interventions. The heterogenous study designs, populations, and measurement protocols adopted by the seven studies within the ILHBN created practical challenges, but also unprecedented opportunities to capitalize on data harmonization to provide comparable views of data from different studies, enhance the quality and utility of expensive and hard-won ILD, and amplify scientific yield. The purpose of this article is to provide a brief report of the challenges, opportunities, and solutions from some of the ILHBN’s cross-study data harmonization efforts. We review the process through which harmonization challenges and opportunities motivated the development of tools and collection of metadata within the ILHBN. A variety of strategies have been adopted within the ILHBN to facilitate harmonization of ecological momentary assessment, location, accelerometer, and participant engagement data while preserving theory-driven heterogeneity and data privacy considerations. Several tools have been developed by the ILHBN to resolve challenges in integrating ILD across multiple data streams and time scales both within and across studies. Harmonization of distinct longitudinal measures, measurement tools, and sampling rates across studies is challenging, but also opens up new opportunities to address cross-cutting scientific themes of interest.
The article shares insights, challenges, opportunities, and solutions from harmonizing intensive longitudinal data within the ILHBN, providing tools and recommendations for future data harmonization efforts.
Addictive Behaviors, Volume 136, p.107467
January 2023
just-in-time adaptive intervention, micro-randomized trial, mindfulness; smoking cessation; mHealth
Smoking cessation treatments that are easily accessible and deliver intervention content at vulnerable moments (e.g., high negative affect) have great potential to impact tobacco abstinence. The current study examined the feasibility and acceptability of a multi-component Just-In-Time Adaptive Intervention (JITAI) for smoking cessation. Daily smokers interested in quitting were consented to participate in a 6-week cessation study. Visit 1 occurred 4 days pre-quit, Visit 2 was on the quit day, Visit 3 occurred 3 days post-quit, Visit 4 was 10 days post-quit, and Visit 5 was 28 days post-quit. During the first 2 weeks (Visits 1-4), the JITAI delivered brief mindfulness/motivational strategies via smartphone in real-time based on negative affect or smoking behavior detected by wearable sensors. Participants also attended 5 in-person visits, where brief cessation counseling (Visits 1-4) and nicotine replacement therapy (Visits 2-5) were provided. Outcomes were feasibility and acceptability; biochemically-confirmed abstinence was also measured. Participants (N = 43) were 58.1 % female (AgeMean = 49.1, mean cigarettes per day = 15.4). Retention through follow-up was high (83.7 %). For participants with available data (n = 38), 24 (63 %) met the benchmark for sensor wearing, among whom 16 (67 %) completed at least 60 % of strategies. Perceived ease of wearing sensors (Mean = 5.1 out of 6) and treatment satisfaction (Mean = 3.6 out of 4) were high. Biochemically-confirmed abstinence was 34 % at Visit 4 and 21 % at Visit 5. Overall, the feasibility of this novel multi-component intervention for smoking cessation was mixed but acceptability was high. Future studies with improved technology will decrease participant burden and better detect key intervention moments.
The study assessed the feasibility and acceptability of a multi-component Just-In-Time Adaptive Intervention (JITAI) for smoking cessation, utilizing smartphone-delivered mindfulness/motivational strategies based on real-time negative affect or smoking behavior detected by wearable sensors. Participants showed high retention (83.7%) and reported high satisfaction with the intervention, but the feasibility was mixed.
Proceedings of the ACM on Interactive, Mobile, Wearable and Ubiquitous Technologies
mobile health, context, smoking cessation, intervention, GPS traces
March 2020
Context plays a key role in impulsive adverse behaviors such as fights, suicide attempts, binge-drinking, and smoking lapse. Several contexts dissuade such behaviors, but some may trigger adverse impulsive behaviors. We define these latter contexts as ‘opportunity’ contexts, as their passive detection from sensors can be used to deliver context-sensitive interventions. In this paper, we define the general concept of ‘opportunity’ contexts and apply it to the case of smoking cessation. We operationalize the smoking ‘opportunity’ context, using self-reported smoking allowance and cigarette availability. We show its clinical utility by establishing its association with smoking occurrences using Granger causality. Next, we mine several informative features from GPS traces, including the novel location context of smoking spots, to develop the SmokingOpp model for automatically detecting the smoking ‘opportunity’ context. Finally, we train and evaluate the SmokingOpp model using 15 million GPS points and 3,432 self-reports from 90 newly abstinent smokers in a smoking cessation study.
In this paper, we define the general concept of ‘opportunity’ contexts and apply it to the case of smoking cessation. We mine several informative features from GPS traces, including the novel location context of smoking spots, to develop the SmokingOpp model for automatically detecting the smoking ‘opportunity’ context.
Contemporary Clinical Trials
engagement, Micro-randomized trial (MRT), mobile health (mHealth), self-regulatory strategies, smoking cessation
November 2021
Smoking is the leading preventable cause of death and disability in the U.S. Empirical evidence suggests that engaging in evidence-based self-regulatory strategies (e.g., behavioral substitution, mindful attention) can improve smokers’ ability to resist craving and build self-regulatory skills. However, poor engagement represents a major barrier to maximizing the impact of self-regulatory strategies. This paper describes the protocol for Mobile Assistance for Regulating Smoking (MARS) – a research study designed to inform the development of a mobile health (mHealth) intervention for promoting real-time, real-world engagement in evidence-based self-regulatory strategies. The study will employ a 10-day Micro-Randomized Trial (MRT) enrolling 112 smokers attempting to quit. Utilizing a mobile smoking cessation app, the MRT will randomize each individual multiple times per day to either: (a) no intervention prompt; (b) a prompt recommending brief (low effort) cognitive and/or behavioral self-regulatory strategies; or (c) a prompt recommending more effortful cognitive or mindfulness-based strategies. Prompts will be delivered via push notifications from the MARS mobile app. The goal is to investigate whether, what type of, and under what conditions prompting the individual to engage in self-regulatory strategies increases engagement. The results will build the empirical foundation necessary to develop a mHealth intervention that effectively utilizes intensive longitudinal self-report and sensor-based assessments of emotions, context and other factors to engage an individual in the type of self-regulatory activity that would be most beneficial given their real-time, real-world circumstances. This type of mHealth intervention holds enormous potential to expand the reach and impact of smoking cessation treatments.
This paper describes the protocol for Mobile Assistance for Regulating Smoking (MARS) – a research study designed to inform the development of a mobile health (mHealth) intervention for promoting real-time, real-world engagement in evidence-based self-regulatory strategies.
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