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SMART 2.0: Social Mobile Approaches to Reducing weighT in Young Adults (SMART 2)

Primary Purpose

Overweight and Obesity

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SMART 2.0
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight and Obesity focused on measuring young adult, overweight, obesity, college, university, technology, social media, text message, health coach, intervention, weight loss, wellness, physical activity, diet, sleep, resilience, wearable, mobile application, behavior mechanism, behavior

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 18 to 35 years
  • Intending to be available for a 24 month intervention
  • Affiliated with either University of California, San Diego (UCSD), San Diego State University (SDSU), or California State University, San Marcos (CSUSM) as a student, faculty, or staff
  • Willing and able to use social media
  • Willing and able to use a smartphone and text messaging
  • Willing and able to use the wearable, scale, and corresponding app
  • Willing and able to attend measurement visits over the 2 year intervention
  • Willing and able to engage in moderate to vigorous physical activity
  • Overweight or obese, but not severely obese (25 >= BMI < 40 kg/m2)

Exclusion Criteria:

  • Any comorbidities of obesity that require a clinical referral including eating disorders, pseudotumor cerebri, sleep apnea or hypoventilation syndrome, orthopedic problems, and meeting American Diabetes Association criteria for diabetes
  • Psychiatric or medical conditions that prohibit compliance with the study protocol
  • Had a cardiovascular event (heart attack, stroke, episode of heart failure, or revascularization procedure) within the last 6 months
  • Currently being treated for a malignancy (other than non-melanoma skin cancer)
  • Currently being treated and/or have an eating disorder
  • Planning to have a weight loss surgery in the next 24 months (e.g., liposuction, lap band, gastric bypass)
  • Pregnant, gave birth within the last 6 months, currently lactating or breastfeeding within the last 3 months, or actively planning pregnancy within the next 24 months
  • Prescribed physical activity and/or dietary changes
  • Prescribed medications that alter weight
  • Enrolled in or planning to enroll in a weight loss program during the study period
  • Lost more than 15 pounds within the past 3 months

Sites / Locations

  • University of California, San Diego

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Treatment One

Treatment Two

Control

Arm Description

Participants assigned to the SMART 2.0 with technology and personal health coaching treatment group (i.e., treatment one) will receive the following: 1) consumer-level wearable and scale with a corresponding app, 2) daily text messages related to physical activity, diet, sleep and weight loss/maintenance, 3) access to SMART 2.0 social media pages and content through an online group with 6 to 12 participants total, and 4) technology-mediated, real-time individual health coaching. Participants will receive 1 to 2 text messages on a daily basis; be asked to use their wearable on a daily basis and self-weigh using the scale at least once per week; be asked to interact with their online group via social media as frequently as possible; and speak with their health coach at a predetermined session schedule.

Participants assigned to the SMART 2.0 technology alone treatment group (i.e., treatment two) will receive the following: 1) consumer-level wearable and scale with a corresponding app, 2) daily text messages related to physical activity, diet, sleep and weight loss/maintenance, and 3) access to SMART 2.0 social media pages and content through an online group with 6 to 12 participants total. Participants will receive 1 to 2 text messages on a daily basis; be asked to use their wearable on a daily basis and self-weigh using the scale at least once per week; and be asked to interact with their online group via social media as frequently as possible.

Participants assigned to the control group will receive a consumer-level wearable and scale with a corresponding app to use at their discretion.

Outcomes

Primary Outcome Measures

Change in weight
Objectively measured weight in kilograms.

Secondary Outcome Measures

Change in Body Mass Index
Weight and height will be combined to report BMI in kg/m^2.
Percent weight change
Percent change in weight from baseline.
Percentage of participants who lost at least 3% of their weight from baseline
Percentage of participants who lost at least 3% of their weight from baseline.
Percentage of participants who lost at least 5% of their weight from baseline
Percentage of participants who lost at least 5% of their weight from baseline.
Change in waist circumference
Objectively measured in centimeters.
Change in waist-to-hip ratio
Waist and hip circumference will be combined to report waist-to-hip ratio in cm/cm.
Change in body composition
Total body and regional (arms, legs, trunk, and abdomen) body composition (fat mass, including an estimate of visceral adipose tissue, and lean mass) measured with Dual-energy X-ray Absorptiometry (DXA).
Change in bone mineral density
Bone mineral density of anterior-posterior spine (L1 - L4), hip, forearm, and total body measured with Dual-energy X-ray Absorptiometry (DXA).
Change in systolic blood pressure
Systolic blood pressure in mmHg.
Change in diastolic blood pressure
Diastolic blood pressure in mmHg.
Change in cardiorespiratory fitness
Three-minute step test.
Change in flexibility
Sit and reach test.
Change in grip strength
Grip strength of the right and left hands in kilograms with a dynamometer.
Physical activity
Measured using Fitbit.
Physical activity
Measured using a waist-worn tri-axial accelerometer.
Change in physical activity
Assessed through self-report using the Global Physical Activity Questionnaire. The questionnaire is comprised of 16 questions related to physical activity in three settings that include activity at work, travel to and from places, and recreational activities, in addition to sedentary behavior. Metabolic Equivalent (MET) values are assigned to time variables according to intensity of activity, moderate or vigorous, reported in each of the settings. MET values are then used to calculate total physical activity.
Sleep
Measured using Fitbit.
Change in sleep
Assessed through self-report using an 8 item self-report questionnaire. Participants respond to questions related to sleep duration and how often they have difficulty falling asleep and staying awake, do not get enough rest.
Resting heart rate
Measured using Fitbit.
Change in resting heart rate
Measured by research assistant.
Sedentary Behavior
Measured using Fitbit.
Sedentary Behavior
Measured using a waist-worn tri-axial accelerometer.
Change in sedentary Behavior
Assessed through self-report using 5 items from the Canadian Fitness Survey and 10 items from the Past-day Adults' Sedentary Time Questionnaire. Participants respond to items from the Canadian Fitness Survey related to how much time participants spend doing sedentary activities on a 5-point response scale ranging from "Almost all of the time" to "Almost none of the time". Participants respond to items from the Past-day Adults' Sedentary Time Questionnaire related to how much time spent sitting while doing activities including working, transportation, etc. using 2 digit entry for hours and minutes. For all items, less time reported doing sedentary activities or sitting represents less sedentary behavior.
Diet History Questionnaire III
The Diet History Questionnaire III contains 135 food and beverage items and 26 dietary supplement items to assess diet consumption for past month. The questionnaire includes additional embedded questions for some items to assess frequency and portion size.
Weight Management Practices
Assessed through self-report using a 3-item questionnaire. Participants respond to items related to which behaviors they have engaged in in the past 30 days to lose weight, how often they weigh themselves using a 6 point response scale ranging from "Never" to "More than once a day", and whether they have access to a scale at home.
Strategies for Weight Management Questionnaire
Strategies for Weight Management Questionnaire consists of 35 items that assess how often participants use of behavioral strategies for reducing energy intake and increasing energy expenditure on a 5-point response scale ranging from "Never or hardly ever" to "Always or almost always". Values which indicate a higher frequency of strategies, "Much of the time" and "Always or almost always", show improved weight management.
Assessment of Eating Behaviors
Assessment of Eating Behaviors survey consists of 8 items that assess sugar sweetened beverage consumption and frequency of eating away from home on a 9-point response scale ranging from "Never or rarely" to "3 or more times per day".
Daily Meal Patterns
Assessed through self-report using a 7-item questionnaire. Participants respond to items related to how often they eat meals and snacks in a typical week using a 5-point response scale ranging from "0 times" to "7 times".
Healthy Eating: Change Strategies
Healthy Eating: Change Strategies survey consists of 15-items that assess how often participants engage in strategies that help them change their dietary habits in the past month using a 5-point response scale ranging from "Never" to "Many times".
Physical Activity: Change Strategies
Physical Activity: Change Strategies survey consists of 15-items that assess how often participants engage in strategies that help them change their physical activity in the past month using a 5-point response scale ranging from "Never" to "Many times".
Physical Activity Neighborhood Environment
Physical Activity Neighborhood Environment survey consists of 17-items that assess the environmental factors for walking and bicycling in various neighborhoods. Higher values from the scale indicate greater environmental support for physical activity.
Social Support for Healthy Eating Habits
Social Support for Diet survey consists of 10-items that assess perceived social support specific to health-related eating behaviors from family and friends, respectively. Each item uses a 8-point response scale that includes "does not apply" and ranges from "none" to "very often".
Social Support for Physical Activity
Assessed using the Physical Activity and Social Support Scale which consists of 20-items scale based in five forms of social support - companionship, emotional, instrumental, informational, and validation for physical activity. Participants respond to items on a 7-point Likert scale ranging from "never" to "always", or "not applicable".
Depression
Assessed using the Center for Epidemiologic Studies depression scale which consists of 10-items. Participants respond to items related to how they feel and behave on a 5-point response scale ranging from "Rarely or none of the time" to "All of the time". A score equal to or above 10 is considered depressed.
Anxiety
Assessed using the short-form of the state scale of the Spielberger State Trait Anxiety Inventory which consists of 6 items. Participants respond to items related to how they feel on a 4-point response scale ranging from "Not at all" to "Very much".
Self-esteem
Assessed using the Rosenberg Self-esteem Scale which consists of 10-items. Participants respond to items related to items related to global self-worth on a 4-point Likert scale ranging from "strongly agree" to "strongly disagree". Higher scores indicate higher self-esteem.
Quality of Well-being
Assessed using the Quality of Well-being survey, self-administered version which consists of 71 items. Participants respond to items related to health status and overall well-being over the previous 3 days. Scores are translated to quality-adjusted life years.
Body Image
Assessed using the Eating Disorder Inventory, Body Dissatisfaction sub scale which consists of 9-items. Participants respond to items related to their body image on a 6-point response scale ranging from "Never" to "Always".

Full Information

First Posted
March 27, 2019
Last Updated
March 13, 2023
Sponsor
University of California, San Diego
Collaborators
National Institutes of Health (NIH), Small Steps Labs, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03907462
Brief Title
SMART 2.0: Social Mobile Approaches to Reducing weighT in Young Adults
Acronym
SMART 2
Official Title
SMART 2.0: Social Mobile Approaches to Reducing weighT in Young Adults
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
February 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
National Institutes of Health (NIH), Small Steps Labs, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The SMART 2.0 study is a 24-month trial designed to evaluate the impact of the intervention with technology and personal health coaching or with technology alone on objectively measured weight among overweight young adults in a university setting over 24 months compared to a control group. The investigators hypothesize that both interventions will significantly improve weight compared to the control group, and the group receiving personal health coaching will experience the greatest improvement.
Detailed Description
Weight gain is an important issue for young adults. Throughout the transition from adolescence to early adulthood, young adults encounter multiple stressors and influences that can contribute to weight gain. In turn, weight gain leads to increased risk of cardiovascular disease, diabetes, and other health issues. Thus, there is a critical need to advance our understanding of how to develop and deploy multimodal, technology-based weight-loss interventions that have the potential for long-term effects and widespread dissemination among young adults. The SMART 2.0 study is a 24-month (96 week) parallel-group randomized control trial designed to evaluate the impact of the interventions on objectively measured weight in kg over 24 months compared to a control group. The study will recruit 642 overweight/obese young adults aged 18-35 at universities in San Diego, CA. Participants will be randomly assigned to one of three groups for a 24-month study period. The three groups include: 1) SMART 2.0 with a consumer-level wearable and scale, text messaging, social media, and technology-based health coaching; 2) SMART 2.0 with a consumer-level wearable and scale, text messaging, and social media; and 3) a control group with a consumer-level wearable and scale alone. Theory- and evidence-based content will be framed around a minimum goal of 5-10% weight loss through increased energy expenditure, decreased energy intake, and adequate sleep. Additionally, participants will be encouraged to lose 1 to 2 pounds per week until they reach a body mass index (BMI) below 25 kg/m2. Once a participant reaches a BMI less than 25 kg/m2 the goal will be to maintain their weight loss. SMART 2.0 uses a fully integrated system of modalities that includes: 1) a popular consumer-level wearable (e.g., Fitbit Charge 3), wireless scale (e.g., Aria Scale), and corresponding app (e.g., the Fitbit app); 2) a highly tailored and interactive text messaging system; 3) multiple social media streams (e.g., Facebook, Facebook Messenger, Instagram, and Twitter); and 4) social network mechanisms of influence. The consumer-level devices and app will be used to self-monitor behavior, and their data will be passively acquired in real-time. Algorithms will be used to automatically deliver text messages to support individually tailored goal setting, performance feedback, and goal review in a highly dynamic style that reflects participants' behavioral progress towards achieving a minimum goal of 5% weight loss. Participants will be encouraged to share their data and behavioral progress with others via social networking tools. Social network mechanisms of influence will be used both within the study-space, to elicit participant-to-participant and health coach-to-participant support, as well as outside the study-space, to invoke social support and accountability from strong ties known to be important for long-term behavior change. Additionally, one group will receive monthly technology-mediated and real-time personal health coaching that is theory- and evidence-based.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity
Keywords
young adult, overweight, obesity, college, university, technology, social media, text message, health coach, intervention, weight loss, wellness, physical activity, diet, sleep, resilience, wearable, mobile application, behavior mechanism, behavior

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is a 24-month parallel-group randomized controlled trial.
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
638 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment One
Arm Type
Experimental
Arm Description
Participants assigned to the SMART 2.0 with technology and personal health coaching treatment group (i.e., treatment one) will receive the following: 1) consumer-level wearable and scale with a corresponding app, 2) daily text messages related to physical activity, diet, sleep and weight loss/maintenance, 3) access to SMART 2.0 social media pages and content through an online group with 6 to 12 participants total, and 4) technology-mediated, real-time individual health coaching. Participants will receive 1 to 2 text messages on a daily basis; be asked to use their wearable on a daily basis and self-weigh using the scale at least once per week; be asked to interact with their online group via social media as frequently as possible; and speak with their health coach at a predetermined session schedule.
Arm Title
Treatment Two
Arm Type
Experimental
Arm Description
Participants assigned to the SMART 2.0 technology alone treatment group (i.e., treatment two) will receive the following: 1) consumer-level wearable and scale with a corresponding app, 2) daily text messages related to physical activity, diet, sleep and weight loss/maintenance, and 3) access to SMART 2.0 social media pages and content through an online group with 6 to 12 participants total. Participants will receive 1 to 2 text messages on a daily basis; be asked to use their wearable on a daily basis and self-weigh using the scale at least once per week; and be asked to interact with their online group via social media as frequently as possible.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants assigned to the control group will receive a consumer-level wearable and scale with a corresponding app to use at their discretion.
Intervention Type
Behavioral
Intervention Name(s)
SMART 2.0
Intervention Description
SMART 2.0 uses a fully integrated system of modalities that includes: 1) a popular consumer-level wearable, wireless scale, and corresponding app; 2) a highly tailored and interactive text messaging system; 3) multiple social media streams; 4) social network mechanisms of influence; and 5) technology-mediated health coaching.
Primary Outcome Measure Information:
Title
Change in weight
Description
Objectively measured weight in kilograms.
Time Frame
Baseline, 24 months
Secondary Outcome Measure Information:
Title
Change in Body Mass Index
Description
Weight and height will be combined to report BMI in kg/m^2.
Time Frame
Baseline, 24 months
Title
Percent weight change
Description
Percent change in weight from baseline.
Time Frame
Baseline, 24 months
Title
Percentage of participants who lost at least 3% of their weight from baseline
Description
Percentage of participants who lost at least 3% of their weight from baseline.
Time Frame
Baseline, 24 months
Title
Percentage of participants who lost at least 5% of their weight from baseline
Description
Percentage of participants who lost at least 5% of their weight from baseline.
Time Frame
Baseline, 24 months
Title
Change in waist circumference
Description
Objectively measured in centimeters.
Time Frame
Baseline, 24 months
Title
Change in waist-to-hip ratio
Description
Waist and hip circumference will be combined to report waist-to-hip ratio in cm/cm.
Time Frame
Baseline, 24 months
Title
Change in body composition
Description
Total body and regional (arms, legs, trunk, and abdomen) body composition (fat mass, including an estimate of visceral adipose tissue, and lean mass) measured with Dual-energy X-ray Absorptiometry (DXA).
Time Frame
Baseline, 24 months
Title
Change in bone mineral density
Description
Bone mineral density of anterior-posterior spine (L1 - L4), hip, forearm, and total body measured with Dual-energy X-ray Absorptiometry (DXA).
Time Frame
Baseline, 24 months
Title
Change in systolic blood pressure
Description
Systolic blood pressure in mmHg.
Time Frame
Baseline, 24 months
Title
Change in diastolic blood pressure
Description
Diastolic blood pressure in mmHg.
Time Frame
Baseline, 24 months
Title
Change in cardiorespiratory fitness
Description
Three-minute step test.
Time Frame
Baseline, 24 months
Title
Change in flexibility
Description
Sit and reach test.
Time Frame
Baseline, 24 months
Title
Change in grip strength
Description
Grip strength of the right and left hands in kilograms with a dynamometer.
Time Frame
Baseline, 24 months
Title
Physical activity
Description
Measured using Fitbit.
Time Frame
Through study completion, up to 24 months
Title
Physical activity
Description
Measured using a waist-worn tri-axial accelerometer.
Time Frame
For 7 days, at 24 months
Title
Change in physical activity
Description
Assessed through self-report using the Global Physical Activity Questionnaire. The questionnaire is comprised of 16 questions related to physical activity in three settings that include activity at work, travel to and from places, and recreational activities, in addition to sedentary behavior. Metabolic Equivalent (MET) values are assigned to time variables according to intensity of activity, moderate or vigorous, reported in each of the settings. MET values are then used to calculate total physical activity.
Time Frame
Baseline, 24 months
Title
Sleep
Description
Measured using Fitbit.
Time Frame
Through study completion, up to 24 months
Title
Change in sleep
Description
Assessed through self-report using an 8 item self-report questionnaire. Participants respond to questions related to sleep duration and how often they have difficulty falling asleep and staying awake, do not get enough rest.
Time Frame
Baseline, 24 months
Title
Resting heart rate
Description
Measured using Fitbit.
Time Frame
Through study completion, up to 24 months
Title
Change in resting heart rate
Description
Measured by research assistant.
Time Frame
Baseline, 24 months
Title
Sedentary Behavior
Description
Measured using Fitbit.
Time Frame
Through study completion, up to 24 months
Title
Sedentary Behavior
Description
Measured using a waist-worn tri-axial accelerometer.
Time Frame
For 7 days, at 24 months
Title
Change in sedentary Behavior
Description
Assessed through self-report using 5 items from the Canadian Fitness Survey and 10 items from the Past-day Adults' Sedentary Time Questionnaire. Participants respond to items from the Canadian Fitness Survey related to how much time participants spend doing sedentary activities on a 5-point response scale ranging from "Almost all of the time" to "Almost none of the time". Participants respond to items from the Past-day Adults' Sedentary Time Questionnaire related to how much time spent sitting while doing activities including working, transportation, etc. using 2 digit entry for hours and minutes. For all items, less time reported doing sedentary activities or sitting represents less sedentary behavior.
Time Frame
Baseline, 24 months
Title
Diet History Questionnaire III
Description
The Diet History Questionnaire III contains 135 food and beverage items and 26 dietary supplement items to assess diet consumption for past month. The questionnaire includes additional embedded questions for some items to assess frequency and portion size.
Time Frame
Baseline, 24 months
Title
Weight Management Practices
Description
Assessed through self-report using a 3-item questionnaire. Participants respond to items related to which behaviors they have engaged in in the past 30 days to lose weight, how often they weigh themselves using a 6 point response scale ranging from "Never" to "More than once a day", and whether they have access to a scale at home.
Time Frame
Baseline, 24 months
Title
Strategies for Weight Management Questionnaire
Description
Strategies for Weight Management Questionnaire consists of 35 items that assess how often participants use of behavioral strategies for reducing energy intake and increasing energy expenditure on a 5-point response scale ranging from "Never or hardly ever" to "Always or almost always". Values which indicate a higher frequency of strategies, "Much of the time" and "Always or almost always", show improved weight management.
Time Frame
Baseline, 24 months
Title
Assessment of Eating Behaviors
Description
Assessment of Eating Behaviors survey consists of 8 items that assess sugar sweetened beverage consumption and frequency of eating away from home on a 9-point response scale ranging from "Never or rarely" to "3 or more times per day".
Time Frame
Baseline, 24 months
Title
Daily Meal Patterns
Description
Assessed through self-report using a 7-item questionnaire. Participants respond to items related to how often they eat meals and snacks in a typical week using a 5-point response scale ranging from "0 times" to "7 times".
Time Frame
Baseline, 24 months
Title
Healthy Eating: Change Strategies
Description
Healthy Eating: Change Strategies survey consists of 15-items that assess how often participants engage in strategies that help them change their dietary habits in the past month using a 5-point response scale ranging from "Never" to "Many times".
Time Frame
Baseline, 24 months
Title
Physical Activity: Change Strategies
Description
Physical Activity: Change Strategies survey consists of 15-items that assess how often participants engage in strategies that help them change their physical activity in the past month using a 5-point response scale ranging from "Never" to "Many times".
Time Frame
Baseline, 24 months
Title
Physical Activity Neighborhood Environment
Description
Physical Activity Neighborhood Environment survey consists of 17-items that assess the environmental factors for walking and bicycling in various neighborhoods. Higher values from the scale indicate greater environmental support for physical activity.
Time Frame
Baseline, 24 months
Title
Social Support for Healthy Eating Habits
Description
Social Support for Diet survey consists of 10-items that assess perceived social support specific to health-related eating behaviors from family and friends, respectively. Each item uses a 8-point response scale that includes "does not apply" and ranges from "none" to "very often".
Time Frame
Baseline, 24 months
Title
Social Support for Physical Activity
Description
Assessed using the Physical Activity and Social Support Scale which consists of 20-items scale based in five forms of social support - companionship, emotional, instrumental, informational, and validation for physical activity. Participants respond to items on a 7-point Likert scale ranging from "never" to "always", or "not applicable".
Time Frame
Baseline, 24 months
Title
Depression
Description
Assessed using the Center for Epidemiologic Studies depression scale which consists of 10-items. Participants respond to items related to how they feel and behave on a 5-point response scale ranging from "Rarely or none of the time" to "All of the time". A score equal to or above 10 is considered depressed.
Time Frame
Baseline, 24 months
Title
Anxiety
Description
Assessed using the short-form of the state scale of the Spielberger State Trait Anxiety Inventory which consists of 6 items. Participants respond to items related to how they feel on a 4-point response scale ranging from "Not at all" to "Very much".
Time Frame
Baseline, 24 months
Title
Self-esteem
Description
Assessed using the Rosenberg Self-esteem Scale which consists of 10-items. Participants respond to items related to items related to global self-worth on a 4-point Likert scale ranging from "strongly agree" to "strongly disagree". Higher scores indicate higher self-esteem.
Time Frame
Baseline, 24 months
Title
Quality of Well-being
Description
Assessed using the Quality of Well-being survey, self-administered version which consists of 71 items. Participants respond to items related to health status and overall well-being over the previous 3 days. Scores are translated to quality-adjusted life years.
Time Frame
Baseline, 24 months
Title
Body Image
Description
Assessed using the Eating Disorder Inventory, Body Dissatisfaction sub scale which consists of 9-items. Participants respond to items related to their body image on a 6-point response scale ranging from "Never" to "Always".
Time Frame
Baseline, 24 months
Other Pre-specified Outcome Measures:
Title
Smoking & Marijuana Use
Description
Assessed using modified items from the Customary Drinking and Drug Use Record. Participants will respond to 26 items related to their smoking and marijuana use over the past 6 months.
Time Frame
Baseline, 24 months
Title
Alcohol Use
Description
Assessed using modified items from the Customary Drinking and Drug Use Record. Participants will respond to 10 items related to their alcohol use over the past 6 months.
Time Frame
Baseline, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 to 35 years Intending to be available for a 24 month intervention Affiliated with either University of California, San Diego (UCSD), San Diego State University (SDSU), or California State University, San Marcos (CSUSM) as a student, faculty, or staff Willing and able to use social media Willing and able to use a smartphone and text messaging Willing and able to use the wearable, scale, and corresponding app Willing and able to attend measurement visits over the 2 year intervention Willing and able to engage in moderate to vigorous physical activity Overweight or obese, but not severely obese (25 >= BMI < 40 kg/m2) Exclusion Criteria: Any comorbidities of obesity that require a clinical referral including eating disorders, pseudotumor cerebri, sleep apnea or hypoventilation syndrome, orthopedic problems, and meeting American Diabetes Association criteria for diabetes Psychiatric or medical conditions that prohibit compliance with the study protocol Had a cardiovascular event (heart attack, stroke, episode of heart failure, or revascularization procedure) within the last 6 months Currently being treated for a malignancy (other than non-melanoma skin cancer) Currently being treated and/or have an eating disorder Planning to have a weight loss surgery in the next 24 months (e.g., liposuction, lap band, gastric bypass) Pregnant, gave birth within the last 6 months, currently lactating or breastfeeding within the last 3 months, or actively planning pregnancy within the next 24 months Prescribed physical activity and/or dietary changes Prescribed medications that alter weight Enrolled in or planning to enroll in a weight loss program during the study period Lost more than 15 pounds within the past 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Job G Godino, PhD
Organizational Affiliation
University of California, San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Diego
City
La Jolla
State/Province
California
ZIP/Postal Code
92093
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27426247
Citation
Godino JG, Merchant G, Norman GJ, Donohue MC, Marshall SJ, Fowler JH, Calfas KJ, Huang JS, Rock CL, Griswold WG, Gupta A, Raab F, Fogg BJ, Robinson TN, Patrick K. Using social and mobile tools for weight loss in overweight and obese young adults (Project SMART): a 2 year, parallel-group, randomised, controlled trial. Lancet Diabetes Endocrinol. 2016 Sep;4(9):747-755. doi: 10.1016/S2213-8587(16)30105-X. Epub 2016 Jul 14.
Results Reference
background
PubMed Identifier
34980208
Citation
Mansour-Assi SJ, Golaszewski NM, Costello VL, Wing D, Persinger H, Coleman A, Lytle L, Larsen BA, Jain S, Weibel N, Rock CL, Patrick K, Hekler E, Godino JG. Social Mobile Approaches to Reducing Weight (SMART) 2.0: protocol of a randomized controlled trial among young adults in university settings. Trials. 2022 Jan 3;23(1):7. doi: 10.1186/s13063-021-05938-7.
Results Reference
derived

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SMART 2.0: Social Mobile Approaches to Reducing weighT in Young Adults

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