key: cord-0863801-xcpn4hrz
authors: Mansour-Assi, Shadia J.; Golaszewski, Natalie M.; Costello, Victoria Lawhun; Wing, David; Persinger, Hailey; Coleman, Aaron; Lytle, Leslie; Larsen, Britta A.; Jain, Sonia; Weibel, Nadir; Rock, Cheryl L.; Patrick, Kevin; Hekler, Eric; Godino, Job G.
title: Social Mobile Approaches to Reducing Weight (SMART) 2.0: protocol of a randomized controlled trial among young adults in university settings
date: 2022-01-03
journal: Trials
DOI: 10.1186/s13063-021-05938-7
sha: 0d6e01b07883dfb35467c246df3dd96b38d84108
doc_id: 863801
cord_uid: xcpn4hrz

BACKGROUND: Excess weight gain in young adulthood is associated with future weight gain and increased risk of chronic disease. Although multimodal, technology-based weight-loss interventions have the potential to promote weight loss among young adults, many interventions have limited personalization, and few have been deployed and evaluated for longer than a year. We aim to assess the effects of a highly personalized, 2-year intervention that uses popular mobile and social technologies to promote weight loss among young adults. METHODS: The Social Mobile Approaches to Reducing Weight (SMART) 2.0 Study is a 24-month parallel-group randomized controlled trial that will include 642 overweight or obese participants, aged 18–35 years, from universities and community colleges in San Diego, CA. All participants receive a wearable activity tracker, connected scale, and corresponding app. Participants randomized to one intervention group receive evidence-based information about weight loss and behavior change techniques via personalized daily text messaging (i.e., SMS/MMS), posts on social media platforms, and online groups. Participants in a second intervention group receive the aforementioned elements in addition to brief, technology-mediated health coaching. Participants in the control group receive a wearable activity tracker, connected scale, and corresponding app alone. The primary outcome is objectively measured weight in kilograms over 24 months. Secondary outcomes include anthropometric measurements; physiological measures; physical activity, diet, sleep, and psychosocial measures; and engagement with intervention modalities. Outcomes are assessed at baseline and 6, 12, 18, and 24 months. Differences between the randomized groups will be analyzed using a mixed model of repeated measures and will be based on the intent-to-treat principle. DISCUSSION: We hypothesize that both SMART 2.0 intervention groups will significantly improve weight loss compared to the control group, and the group receiving health coaching will experience the greatest improvement. We further hypothesize that differences in secondary outcomes will favor the intervention groups. There is a critical need to advance understanding of the effectiveness of multimodal, technology-based weight-loss interventions that have the potential for long-term effects and widespread dissemination among young adults. Our findings should inform the implementation of low-cost and scalable interventions for weight loss and risk-reducing health behaviors. TRIAL REGISTRATION: ClinicalTrials.govNCT03907462. Registered on April 9, 2019

Overweight and obesity remain major public health concerns in the USA [1, 2] . Recent data from the Centers for Disease Control and Prevention indicate the extent of this problem is great even among young adults. Approximately 62.6% of those 20 to 34 years old are overweight or obese (defined as a body mass index [BMI] ≥ 25 kg/m 2 ) [3] . Excess weight gain occurs most rapidly in young adults and is associated with future weight gain [4, 5] and cardiovascular disease risk factors [6] .

More than half of young adults in the USA are enrolled in tertiary education [5] , and an estimated 40.7% of students are overweight or obese [7] . Engagement in tertiary education represents a period of time when young adults typically undergo the transition from adolescence to young adulthood and often adopt unhealthy weightrelated behaviors, such as decreased physical activity [8] [9] [10] , poor diet quality [8, 9, 11] , and poor sleep hygiene [8, 9] . Consequently, many young adults gain weight while in the university or college settings, suggesting a need for evidence-based weight loss interventions that target this population during this transition [12] .

One potential strategy is to deploy interventions designed to promote weight loss through healthy changes in physical activity, diet, and sleep [13] [14] [15] via mobile and social technologies that are highly pervasive in the USA. For example, approximately 96% of young adults own a smartphone, and 77% of them use it to get information about their health [16, 17] . Furthermore, 21% of adults in the USA regularly wear an activity tracker or smartwatch that monitors health-related outcomes, and device ownership is predicted to rise considerably in the coming years [18] . Social media use among young adults is also ubiquitous, with an estimated 88% using at least one platform regularly and no differences in use by sex, race, or ethnicity [19] . Facebook remains the most popular platform among all adults, and overall engagement is increasing. As many as 70% of adults between the ages of 18 and 29 years old use Facebook daily, and other platforms such as Instagram and Twitter are widely used [19] . Thus, instead of relying on in-person interactions as weight loss interventions have traditionally done [10, [20] [21] [22] [23] , interventions can utilize mobile-and social media-based modalities to meet young adults in the virtual spaces they frequently inhabit [24, 25] . The flexibility and scalability of this approach may be more acceptable than in-person approaches among this young adult population [26] .

Although digital behavior change interventions (DBCI) have shown promising results for weight loss, few studies target young adults and have limited personalization, duration, and modalities [27, 28] . A majority of DBCIs that target weight loss have been conducted exclusively among middle-aged and older adults [27, 28] . Additionally, a minority of interventions include a high level of personalization and multiple behavior change techniques, and few interventions have been implemented for longer than 18 months [27, 28] . The use of several modalities would allow for greater personalization and exposure to intervention content; however, one systematic review found that of the 139 DBCIs included in the review, 60.4% of interventions identified used only one modality, 33.8% two, 5.0% three, and only one used five [28] . Despite these shortcomings, two systematic reviews and meta-analyses have shown that on average, DBCIs can achieve moderate weight loss (− 2.77 kg, 95% CI − 3.54 to − 2.00 kg [27] ; − 2.70 95% CI − 3.33 and − 2.08 kg [28] ). Thus, there remains a need for long-term, multimodal DBCIs that target weight loss and have the potential for enhanced effect sizes and widespread dissemination among young adults.

The primary objective of the Social Mobile Approaches to Reducing Weight (SMART) 2.0 Study is to determine the effectiveness of our evidence-based, multimodal SMART 2.0 interventions to improve objectively measured weight loss in kilograms over 24 months (96 weeks) compared to a control group. The SMART 2.0 intervention approach is built upon previous DBCIs [29] [30] [31] , and the study is designed to evaluate the extent to which brief, technology-mediated health coaching might enhance the intervention effects. The secondary objectives are to evaluate the differences between the groups at 6, 12, 18, and 24 months in anthropometric and physiological outcomes, physical activity, diet, sleep, self-esteem, body image, anxiety, and depression. Additional analyses will examine the dose response (i.e., quantified engagement with technological modalities and behavior change techniques) of the intervention, the usability and acceptability of the intervention, potential mediators and moderators of the intervention effects (e.g., contamination), and patterns of change in physical activity, diet, and sleep.

The SMART 2.0 Study is a 24-month (96 weeks) parallel-group randomized controlled trial where 642 overweight and obese young adults, aged 18-35, in San Diego, CA, are randomized to one of three study groups. Participants in each group receive a consumer-level wearable activity tracker and connected scale from Fitbit, which includes access to the Fitbit smartphone and webbased application (app) ecosystem (https://www.fitbit. com/global/us/home). Participants assigned to the control group receive only these technology components. Participants assigned to intervention group 1 (IG1) also receive personalized daily text messages (i.e., SMS/ MMS) related to physical activity, diet, sleep, resilience, and weight loss, and access to information about weight loss through study social media pages and a study interventionist-moderated online group. Participants assigned to intervention group 2 (IG2) receive everything that IG1 receives in combination with brief, technologymediated health coaching. The sponsor and funder, the National Institute of Health, played no part in the study design. They have no role in the collection, management, analysis, and interpretation of the data. They played no part in the writing of the protocol and the decision to submit the protocol for publication. More details on the intervention components are provided below. The study used SPIRIT reporting guidelines [32] and the design and flow of participants are shown in Fig. 1 .

Young adults aged 18-35 years are recruited from 3 universities and 5 community colleges in San Diego, CA. The eligibility criteria include (1) overweight or obese (25 ≤ BMI < 40 kg/m 2 ); (2) available for a 24-month intervention; (3) affiliated with a San Diego University or college as a student, staff, or alumni; (4) willing and able to use social media, a smartphone, text messaging, and Fitbit devices and app; and (5) willing and able to engage in moderate to vigorous physical activity (MVPA). The exclusion criteria include (1) comorbidities of obesity that require a clinical referral or conditions that prohibit compliance with the study protocol, (2) a recent cardiovascular event, (3) currently being treated for malignancy and/or an eating disorder, (4) planning to have weight loss surgery or enroll in a weight loss program, (5) loss of more than 15 pounds within the past 3 months, and (6) pregnancy or planning pregnancy within 24 months.

Participants are recruited through digital advertisements on campus platforms, targeted social media advertisements, print and digital flyers, email listservs, and campus-wide events. Interested individuals are directed to an online link that includes a description of the study purpose, procedures, risks and benefits, and a secure online screening form. The eligibility criteria are confirmed through telephone screening with the study staff. Participants who meet the eligibility requirements are invited to schedule a baseline appointment at the Exercise and Physical Activity Resource Center at the University of California, San Diego. There, participants are rescreened for the inclusion and exclusion criteria, provided written informed consent, and completed the baseline measurement.

To increase enrollment and retention in the study, Fitbit devices and incentives in the form of cash payments and gift cards are provided to all participants. At baseline, each participant receives a wearable activity tracker and connected scale from Fitbit to use throughout the study and keep after study participation is completed. Incentive payments of $20, $25, $25, and $30 are provided at the 6-, 12-, 18-, and 24-month follow-up measurement visits, respectively. Additionally, participants are able to receive the incentive payment for any missed measurement visit(s) if they return for a subsequent visit. For example, if a participant missed their 12-month measurement visit, they are offered $50 ($25 + $25) as compensation for returning for the 18-month visit. Participants affiliated with non-UCSD campuses receive an additional $15 for each measurement visit to compensate for additional travel costs. The appointment scheduling strategy includes automated email reminders sent 3 months prior to each intended measurement visit; continued phone, email, and text message outreach; and flexible scheduling. Lastly, while UCSD in-person research was suspended (March 2020 to August 2020) and is limited (August 2020 to present) to mitigate the spread of COVID-19, remote follow-up measurement visits are offered to participants unable to return to campus. This includes completing self-report surveys online followed by a self-administered weigh-in using their connected scale.

After eligibility and consent are confirmed and baseline measurements are completed, participants are stratified by sex and university/college and then randomized within each stratum at a ratio of 1:1:1 to one of three groups: (1) SMART 2.0 with technology alone (IG1), (2) SMART 2.0 with technology and health coaching (IG2), or (3) a control group receiving only a Fitbit tracker and scale. Each university or college was organized into three strata depending on the nearness of their campus locations. These strata include the following: College, and MiraCosta Community College. An electronic randomization list was generated using the latest version of the statistical software platform R (version 3.3.2, http://www.r-project.org). The list was securely integrated into the Research Electronic Data Capture (REDCap) tool hosted at UCSD [33, 34] , and allocation is concealed from all investigators and staff until the study group is assigned. Only the study manager, health coaches, and research assistants involved in the delivery of the intervention are subsequently made aware of the allocation. All staff that measure participants and investigators that conduct the analyses will remain blinded to the allocation throughout the study.

The current study builds on our team of investigators' previous weight loss interventions [29] [30] [31] and addresses newer opportunities for intervention delivery that align with the current state of digital health technology. The ConTxt study, a 12-month personalized text messaging and health coaching intervention, aimed to improve weight among 298 overweight and obese adults, aged [29] . Adults in the intervention showed a weight loss equal to 3.6%, contrasted against those in the control group who lost 0.6% [29] . The SMART study was part of the Early Adult Reduction of weight through LifestYle (EARLY) trials, a consortium of weight loss studies among young adults [31] . SMART, a 24-month DBCI, used mobile and social technologies (i.e., mobile apps, text messaging, Facebook, emails, a website, and brief health coaching) to improve weight among 404 overweight or obese college students, aged 18-25, from three universities in San Diego, CA. Findings showed significant weight loss (− 1.33 kg) at 6 and 12 months; however, there were no differences at 18 or 24 months [29] . While these studies showed promising findings in improving weight loss, they are not without limitations. Both studies included limited modalities that were not fully integrated into the study design, and participants decreased engagement with technology over time [35] . Findings from exit interviews with 38 participants of the SMART study suggested that an intervention that incorporates popular consumer-level devices and apps, while capitalizing on existing and studyengineered social networks, may be highly engaging to young adults [35] [36] [37] . To improve upon its predecessors, the current study uses a fully integrated, highly-tailored system of modalities.

The delivery of theory-and evidence-based content in the SMART 2.0 intervention is flexible and lends itself well to complex and adaptive technology-based interventions that are responsive to an individual's behavioral progress and ever-changing context [38] [39] [40] [41] . We do not have a single overarching theoretical framework, rather the SMART 2.0 intervention content reflects numerous theoretical orientations (e.g., operant conditioning [42] , theories of social comparison [43] , theories of social support [44] , and ecological theory [45] ). The use of multiple theories to design the intervention represents a strength of our approach [38] [39] [40] [41] . Furthermore, the SMART 2.0 intervention content is mapped directly onto theory-based behavioral change techniques (BCTs). Specifically, the intervention is informed by Abraham and Michie's taxonomy of 93 distinct BCTs clustered into 16 domains [46] . A meta-analysis of 122 evaluations of interventions that targeted healthy changes in physical activity and diet revealed that the most effective BCTs were self-regulatory and included intention formation, goal setting, self-monitoring, feedback, and goal review [47] . Therefore, contents supporting these are delivered via all modalities, along with content supporting BCTs that target social network mechanisms of influence (e.g., social support, comparison of behavior, and restructuring the social environment). All BCTs included in the intervention were classified prior to delivery (Table 1 describes how these are delivered).

Intervention content is also derived from the strategies for weight management (SWMs), which comprise 35 of the most common evidence-based approaches to achieve weight loss (e.g., reduce portion sizes, avoid processed foods, eliminate sugar-sweetened beverages). The SWMs were successfully integrated into previous studies showing efficacy [48, 49] . Additional intervention content is drawn from comprehensive lifestyle interventions that teach stimulus control, problem solving, time management, and stress management [38, 49] .

Intervention SMART 2.0 is a multimodal DBCI. Participants in both treatment groups (IG1 and IG2) set a minimum overall weight loss goal of 5% of their baseline weight. Participants are then encouraged to lose 1-2 lb per week until they reach their overall weight loss goal [50] . If a participant reaches a BMI ≤ 25 kg/m 2 , the goal shifts to weight maintenance. Through the use of a dynamic text messaging system that is directly integrated with Fitbit data, participants are prescribed weekly physical activity, diet, and sleep goals that begin 1 week after the start of Fitbit data collection. Weekly physical activity goals increase incrementally by 20 min of MVPA building to 225 min (3.75 h) [51] . Weekly dietary goals include achieving a reduced energy intake of at least 500 kcal/day [52] , which is monitored through logging dietary consumption via the Fitbit app for 3 consecutive days per week for the first 4 weeks of the intervention, followed by 3 consecutive days per month for the remainder of the study. Weekly sleep goals increase incrementally by 10 min of average nightly sleep building to 420 min (7 h) [53] . Participants are directed to self-monitor their physical activity, diet, and sleep daily and their weight weekly via the Fitbit ecosystem.

The wearable activity tracker and connected scale from Fitbit allow for all participants to monitor physical activity, sleep, and diet. Participants receive either the Fitbit Charge 3 or Fitbit Charge 4 as activity trackers and either the Aria 2 scale or Aria Air scale, depending on which was the current consumer-available device at the time of enrollment. The Fitbit Charge 3 and 4 are wristworn devices that log objective measurements through its triaxial accelerometer, an optical heart rate monitor, and altimeter. The Aria 2 and Aria Air scales are digital, connected scales that measure weight and BMI. Behavioral and anthropometric trends can then be viewed by the participants in real-time via the Fitbit smartphone or web-based app. Data from the devices is passively and securely streamed to the Fitbit website. It is then retrieved using Fitabase (https://www.fitabase.com), a webbased app developed by Small Step Labs for the simultaneous collection of high-resolution Fitbit data from large numbers of participants and integration with a dynamic text messaging system.

Participants in both treatment groups (IG1 and IG2) receive personalized, tailored goals and feedback, and related behavioral change strategies through daily text messages. These tailored text messages require participants to use all five core self-regulation strategies (i.e., self-monitoring, feedback on performance, behavioral intention formation, goal setting, and goal review) and follow a 4-week format, detailed in Fig. 2 . One to two text messages are delivered at a consistent time each day via the Fitabase text message system. Text messages are based on data collected from a participant's use of the wearable activity tracker and connected scale from Fitbit. Goals and feedback are contingent on a participant's weight loss and progress in meeting previous weekly physical activity, diet, and sleep behavior goals. For example, after a participant completes their weekly weigh-in, a message will be sent praising the participant for losing 2 pounds and setting a new weekly weight loss goal of 1-2 lb. Additionally, after a participant reaches a BMI < 25 kg/m 2 , goals related to weight, energy intake, and physical activity are automatically adjusted to reflect weight maintenance. For example, if a participant records an average weekly energy intake that is equal to their average weekly energy expenditure, their diet feedback will praise the participant and suggest continued consistent energy intake to maintain their healthy weight.

After randomization, participants in both treatment groups (IG1 and IG2) are placed in groups of 6 to 10 total participants using Facebook messenger (https:// www.facebook.com). To do so, each participant connects with a study interventionist as a friend on Facebook, who then adds participants to their respective, private groups on Facebook Messenger. Informational content and resources are shared in the groups and are only Restructuring the social environment Social media, online groups -Social media and online groups are used to encourage participants to plan PA-and diet-related behaviors together.

Social media, online groups -Information about where to exercise, eat well, and seek mental health resources on campus sent via social media and online groups.

HC health coaching, PA physical activity accessible to the members of each group a study interventionist. A study interventionist posts content and facilitates group discussion that follows a behavioral weight loss curriculum organized as a series of 24-week (6-month) cycles. This includes knowledge check-ins, shared experiences, and goal setting. A study interventionist monitors all group interactions, responds to inquiries from the participants, and elicits interactions. A study interventionist also posts general content related to weight loss/management, physical activity, healthy eating, sleep, and resilience to the study's Facebook, Instagram, and Twitter pages. Participants are required to "like" the SMART 2.0 Facebook page and are encouraged to "follow" the study's Instagram and Twitter accounts. By "liking" and "following" these respective pages, SMART 2.0 content appears on their individual social media feeds where participants have the option to "like" and "comment" on each post, communicate with other participants through each post, and "save" any content.

Participants randomized to the IG2 intervention arm receive individual technology-mediated, real-time health coaching that is theory-and evidence-based [46, [54] [55] [56] . Health coaching sessions consist of motivational interviewing (MI) [57, 58] , participant-determined behavioral goal setting, accountability for health behaviors, health education, and BCTs appropriate for individual coaching [46, 59] . These BCTs include goal setting, action planning, problem solving, feedback on behavior, social support, and instruction on how to perform a behavior [46] . Sessions last approximately 10 min and take place over the phone and/or through Zoom (https://zoom.us), depending on the participant's preference. Following each session, the health coach sends a session recap via email that includes an outline of what was discussed, a summary of behavioral and weight loss goals, and the date/ time of the next session.

In total, participants in IG2 will receive 38 health coaching sessions across 2 years, as shown in Table 2 . During year 1 of the intervention, the health coaching curriculum follows the year-long CDC's Prevent T2 Lifestyle Change Program (DPP). The goals of the DPP include weight loss of 5-7% of participants' baseline weight in the first 6 months and continued weight loss until participants reach their goal weight [60] . The program emphasizes self-monitoring, self-efficacy, and problem solving and requires weigh-ins at each session and the self-monitoring of diet and physical activity. Health coaches receive this feedback digitally through Health coaches cover the DPP curricula during each session and provide participants with the respective DPP handout via email following each session. The DPP session topics have been tailored for the intervention (e.g., replacing in-person group-based activities with related discussion topics) and for the young adult population (e.g., discussing causes and ways to mitigate stress applicable to participants' lifestyles, such as during final examinations) and is outlined in Table 2 . During year 2 of the intervention, participants in IG2 will continue with monthly 10-min sessions with the health coach. Sessions are guided by the participant's unique behavioral and weight loss goals, rather than predetermined topics used in year 1. Each session also consists of effective health coaching components [54, 56] and BCTs [46] .

Outcome measures are collected at baseline and 6, 12, 18, and 24 months. The primary outcome, body weight, is objectively measured to the nearest 0.1 kg using a calibrated digital scale (Seca703, Seca GmbH & Co. KG., Hamberg, DE). Secondary outcome measures include anthropometric and physiological outcomes; physical activity, diet, and sleep behaviors; psychological measures; and engagement with intervention modalities. Anthropometric measurements follow standardized procedures and are implemented by trained staff. Height is measured to the nearest 0.1 cm using a stadiometer, BMI is calculated from the height and weight as kg/m 2 , waist and hip circumferences are measured to the nearest 0.1 cm using a stretch-resistant measuring tape, and blood pressure and heart rate are measured with a digital monitor (Critikon Dinamap 8100, GE Healthcare, Chalfont, UK). Body composition and bone density are measured with dual-energy X-ray absorptiometry (DXA). Cardiovascular fitness is assessed through the Tecumseh 3-min step test [61] . Grip strength is measured to the nearest kilogram using a calibrated hydraulic dynamometer (Model Bl55001, FEI, White Plains, NY) [62] . Lower limb and back flexibility are measured using a modified sit and reach test [63] . Physical activity and sleep are objectively measured for 7 days consecutively at the baseline and 12-and 24month measurement visits using the validated, waistworn ActiGraph Link (ActiGraph Inc., Pensacola, FL) [64] [65] [66] [67] and continuously through Fitbit Charge. Physical activity and sleep are also measured by self-report through the Global Physical Activity Questionnaire (GPAQ) [68] , Physical Activity Neighborhood Environment Scale (PANES) [69] , and the last 7-day Sedentary and Behavior Questionnaire (SIT-Q-7d) [70] . Social support for engagement in physical activity and sleep are measured using the Physical Activity and Social Support Scale (PASSS) [71] , and behavioral perceptions and intentions are measured using items that have been used in prior behavioral health research [72, 73] . Diet is measured using self-report in the Fitbit app and the Diet History Questionnaire III (DHQ-III) [74] . Social support for engagement in a healthy diet is measured using the Social Support for Diet Survey [75] , and behavioral perceptions and intentions are measured using items that have been used in prior behavioral health research [76, 77] . Engagement in behaviors typically used to achieve weight loss are measured using the strategies for weight management [48] .

Psychological measures include the Center for Epidemiological Studies -Depression (CES-D) scale [78] , Spielberger State Trait Anxiety Inventory (STAI) [79] , Rosenberg Self-Esteem Scale [80] , and Quality of Wellbeing Scale [81] . Among the intervention group participants, objective markers of engagement include usage of the Fitbit wearable activity tracker and connected scale, text messages received, interactions on social media pages and online groups (e.g., liking a post), and amount of health coaching sessions received. At 24 months, usability and acceptability of the intervention are assessed using a Likert scale that asks about the level of satisfaction with the program, each program modality, and overall progress. The enrollment, allocation, and measures are summarized in Table 3 .

The principal investigator will be responsible for monitoring data collection, data quality and timeliness, and monitoring participant recruitment, accrual, and retention. All measures are collected and managed using the secure, HIPAA-compliant web-based tool REDCap [33, 34] hosted at UCSD. REDCap provides an intuitive interface for data entry, audit trails for tracking data manipulation and export procedures, automated export procedures for seamless data downloads to common statistical packages, and procedures for importing data from external sources (e.g., all study anthropometric and physiological measures). Data collected will be kept strictly confidential, accessed only by members of the trial team, and stored on a secure database on REDCap. Each participant will be allocated an individual trial identification number. The study is not exceptionally large or long term, and no planned interim analyses for efficacy or futility will be conducted. Therefore, a Data Safety and Monitoring Board will not be appointed. However, adverse events and unanticipated problems involving risk to participants will be monitored weekly throughout the entirety of the randomized controlled trial and reported to the Human Research Protections Programs (HRPP) at UCSD within 10 days. Anticipated adverse events include muscle or bone injury during physical activity, physical discomfort wearing the Fitbit device, and falling, dizziness, nausea, and fatigue during cardiovascular fitness testing. There is no anticipated harm and compensation for trial participation and, thus, no provisions for post-trial care. Additionally, the investigators will protect the health and safety of participants and pursue the research objectives with scientific diligence by monitoring responses to social and behavioral measures, blood pressure, and changes in weight and will inform participants of information relevant to their continued participation. A fidelity of 5% of health coaching sessions will be evaluated by trained research staff using an adapted ASPIRE-VA health coaching fidelity checklist [82] . The trial team, including investigators and research staff, will meet weekly to review trial conduct, and the principal investigator will report to the Study Steering Committee at regular meetings. HRPP at UCSD will review the conduct annually throughout the trial period. The sponsor, funder, and HRPP will be notified of any potential future protocol amendments prior to implementation, and the protocol will be updated in the clinical trials registry. All protocol deviations will be fully documented using a protocol deviation form. Within 6 months after the completion of study analyses, or upon publication of findings, whichever comes first, data will be made available to the scientific research community via a public website and/or data repository. Any data required to support the protocol can be supplied upon request.

Analyses will be conducted using the latest version of the statistical software platform R and will be based on the intention-to-treat principle. All tests of significance will be two-sided and a p-value of 0.05 will be considered statistically significant. Summary statistics (e.g., mean, standard deviations, proportions) will be calculated for all variables of interest. Outliers will be assessed, and variables whose distributions depart significantly from normality will be transformed. Appropriate non-parametric alternatives will be considered if parametric assumptions fail.

The primary outcome of the study is the change in objectively measured weight in kilograms, and the SMART 2.0 intervention groups will be compared to the control group using a mixed model of repeated measures (MMRM) [83] . The model will include the change in weight from baseline at each post-baseline visit (i.e., 6, 12, 18 , and 24 months) as the dependent variable. Fixed effects will include study group, visit, study group-byvisit interaction, weight at baseline, and any variables determined to be confounders. Visit will be treated as a categorical variable, and an unstructured variancecovariance structure will be used. The results will be reported as point estimates (mean differences between the groups) and interval estimates (95% confidence intervals). An intervention effect will be concluded if the pvalue for the study group-by-visit interaction contrast in the model at 24 months is statistically significant. Holm's method will be used to adjust the two p-values for multiple comparisons [84] . This approach uses all available data and is robust to data missing at random (MAR) [85, 86] . However, two additional approaches may be employed to examine the influence of missing data on the primary outcome analysis (which takes a likelihoodbased approach to estimation but does not directly impute data). First, we will model the probability of missingness as a function of baseline covariates and previous outcomes (using logistic regression). The inverse of the resulting probabilities will serve as propensity scores that will be included in the model of the primary outcome. If data are MAR or the probability of missingness can be fully explained by observable data, this approach produces asymptotically unbiased estimates. Second, in order to allow for the possibility that the MAR assumption may not hold (an assumption that is not empirically testable), we will use pattern mixture models in which the distribution of the primary outcome is assumed to follow a mixture of two distributions: one for those who complete follow-up and another for those who do not. These approaches will allow us to quantify the robustness of the study findings to missing data assumptions. Secondary outcomes will be analyzed using the MMRM approach outlined above to compare the differences between the SMART 2.0 intervention groups and the control group at 6, 12, 18, and 24 months in anthropometric and physiological outcomes, physical activity, diet, sleep, body image, anxiety, depression, and the frequency and composition of participant's online communication about weight-related behaviors (all of these measures are continuous). The dose response (i.e., engagement with intervention modalities) of the SMART 2.0 interventions on outcomes at 6, 12, 18, and 24 months will be examined by including engagement variables as independent variables in multiple regression models with the study outcomes as the dependent variable adjusting for covariates. Factors that may mediate or moderate the effect of the SMART 2.0 interventions on study outcomes will be examined. Mediators (e.g., physical activity, diet, social support) will inform how the intervention may have worked to change the outcome, while moderators (e.g., sex, age, social network connectivity, contamination) will illuminate for whom and under what conditions the intervention may have been efficacious. Mediation will be tested via path analysis with regression paths from randomized group to change in the mediator and from change in the mediator to change in the outcome, along with a direct path from the intervention to change in the outcome. Adding interaction terms to the models assessing the intervention effects will test moderation. For all secondary analyses of interest, no adjustments for multiple comparisons will be made and a p-value of 0.05 will be considered statistically significant.

In order to ensure that the trial has adequate power to determine the effectiveness of the SMART 2.0 intervention to improve weight loss in kiloograms, we calculated the sample size based on a two-sided, two-sample t-test with 80% power at a significance level of 2.5% (a Bonferroni correction to account for two tests). In the SMART study, the standard deviation (SD) of change in weight at 6 and 12 months ranged from 3.87 to 5.97 kg, and we have assumed that the corresponding SD in SMART 2.0 will fall within this range [30] . Furthermore, the smallest statistically significant mean difference in change in weight between the two groups occurred at 12 months and was approximately − 1.33 kg [30] . If we assume an SD of 4.92 and a modest increase in the between-group difference (− 1.60 kg), then we will need 182 subjects per group in order to detect a minimal standardized effect size of 0.33. Thus, we will randomize 642 participants (214 per group accounting for a 15% attrition rate).

There is a need to advance our understanding of the effectiveness of multimodal, technology-based weight-loss interventions that have the potential for long-term effects and widespread dissemination among young adults. By relying on existing mobile and social technology platforms, we are able to meet young adults in the virtual spaces they frequently occupy and deliver evidencebased information about weight loss and behavior change techniques. We hypothesize that both SMART 2.0 intervention groups will significantly improve weight compared to the control group, and the group receiving health coaching will experience the greatest improvement. We further hypothesize that differences in secondary outcomes will favor the intervention groups, with the greatest improvements in the group receiving health coaching. Findings from the SMART 2.0 study will add to the growing evidence on the effectiveness of DBCIs for weight loss among young adults, and the impact of a long-term intervention that utilizes multiple fully integrated modalities. Importantly, the study will provide insights into the impact of different features of DBCIs, including the potential benefit of technology-mediated health coaching. It will also provide a robust examination of changes in anthropometric and physiological outcomes, weight-loss-related behaviors, and psychosocial outcomes over 2 years. We are also able to explore ways in which different modalities provide opportunities for engagement, usability, and acceptability of intervention content, and potential mediators and moderators of the intervention effects. These findings will inform approaches to promoting regular engagement in physical activity, a healthy diet, and adequate quality sleep. Overall, the findings from this study should inform the implementation of low-cost and scalable interventions for weight loss and risk-reducing health behaviors.

This study is approved by the Human Research Protections Programs at UCSD (protocol #181862, version 1). Recruitment began in April 2019 and was completed in November 2021. 

National Institutes of Health (US). The surgeon general's call to action to prevent and decrease overweight and obesity. US: Office of the Surgeon General

Accelerating progress in obesity prevention: solving the weight of the nation

Table 26

Who changes body mass between adolescence and adulthood? Factors predicting change in BMI between 16 year and 30 years in the 1970 British Birth Cohort

College enrollment and work activity of recent high school and college graduates summary

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Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations

We are grateful to the staff of the Exercise and Physical Activity Resource Center at UC San Diego for their contributions to the data collection, and we are also grateful to Marla Sklover for her contributions to the operations and finance.

Authors' contributions JG is the principal investigator; he conceived the study and led the proposal and protocol development. LL, SJ, NW, CR, and KP all contributed to the study design and development of the proposal. SMA, NG, VLC, and EH are involved in the protocol development, study implementation, and dissemination of the findings. HP and AC contributed to the protocol development and delivery of the study. All authors read and approved the final manuscript.

The study is supported by a grant from the National Institute of Health's National Heart Lung and Blood Institute: R01HL136769. Natalie M.Golaszewski is supported by a grant from the National Institute of Health's National Institute on Aging: T32AG058529. The use of REDCap is supported by a grant to the Altman Clinical and Translational Research Institute (UL1TR001442). The funders have no role in the study design, data collection, and analysis; decision to publish; or preparation of the manuscript.

The datasets analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate This study is approved by the Human Research Protections Programs at UCSD (protocol #181862). Written, informed consent to participate is obtained from all participants.

Not applicable.

The authors declare that they have no competing interests.

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