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Avoid and Resist Strategies for Weight Management

Primary Purpose

Obesity, Overweight

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Home food environment and grocery delivery (AVOID)
Inhibitory control training (RESIST)
WW
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria (Main participants):

  • Age 18 years or older
  • BMI between 25-40 kg/m2
  • Read, write, and speak English with acceptable visual acuity

Inclusion Criteria (Household participants):

  • 14-years-old
  • Parent consent for children <18-years-old
  • Willingness to complete assessments / measurements

Exclusion Criteria (Main participants):

  • Currently enrolled in weight loss interventions or undergoing bariatric surgery
  • Pregnant women
  • Individuals for whom weight loss may be contraindicated (e.g., unstable coronary artery disease, end-stage disease, active cancer treatment, uncontrolled insulin-dependent diabetes, portal hypertension, drug/alcohol abuse)
  • Individuals with severe cognitive delays or visual/hearing impairment
  • Individuals who are unable or unwilling to complete the study assessments / measurements

Exclusion Criteria (Household participants):

  • ≤ 14-years-old
  • Individuals who are unable or unwilling to complete the study assessments / measurements

Sites / Locations

  • Cedars-Sinai Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

WW Only

WW + Home modification and grocery delivery (AVOID)

WW + Inhibitory control training (RESIST)

WW + Home food modification and grocery delivery (AVOID) + Inhibitory control training (RESIST)

Arm Description

WW is commercially-available weight management program focusing on diet, physical activity and mindset skills.

WW + modification of home food environment + online grocery shopping and delivery

WW + daily gamified inhibitory control training

WW + modification of home food environment + online grocery shopping and delivery + daily gamified inhibitory control training

Outcomes

Primary Outcome Measures

Change in BMI from baseline to 12 months.
BMI will be calculated by aggregating participants' self-reported height in meters and weight in kilograms at baseline, 6- and 12-months.

Secondary Outcome Measures

Diet quality assessed by 24h-dietary recall
Gold standard interviewer-administered, multi-pass 24h-recalls (2 weekdays, 1 weekend day) will be used to measure diet quality. The Nutrition Data System for Research software (Nutrition Coordinating Center, University of Minnesota) is used to analyze the data. Investigators will use the 24h-recalls to assess changes in participants and household members' overall diet quality, based on adherence to the dietary guidelines for fruits and vegetables, servings of whole grains, red/processed meat, alcoholic beverages and food/beverages with added sugars.

Full Information

First Posted
November 10, 2021
Last Updated
May 22, 2023
Sponsor
Cedars-Sinai Medical Center
Collaborators
University of California, Riverside, Weight Watchers International, The University of Tennessee, Knoxville, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT05143931
Brief Title
Avoid and Resist Strategies for Weight Management
Official Title
Evaluating Environmental Control (AVOID) and Inhibitory Control (RESIST) Strategies to Improve Weight Management Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 6, 2022 (Actual)
Primary Completion Date
December 1, 2026 (Anticipated)
Study Completion Date
February 9, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cedars-Sinai Medical Center
Collaborators
University of California, Riverside, Weight Watchers International, The University of Tennessee, Knoxville, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

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

5. Study Description

Brief Summary
The proposed randomized controlled trial tests two self-regulatory approaches to improve intentional weight loss and diet quality in individuals with overweight or obesity: (1) an environmental control strategy (AVOID) and (2) an impulse control training strategy (RESIST).
Detailed Description
Evidence-based weight management programs are effective when individuals are able to consistently adhere to recommendations. However, a large proportion of treatment-seeking individuals do not experience clinically significant weight loss. Innovative strategies are needed to optimize behavior change in weight management interventions. The proposed randomized controlled trial tests two self-regulatory approaches to improve intentional weight loss and diet quality in individuals with overweight or obesity: (1) an environmental control strategy (AVOID) and (2) an impulse control training strategy (RESIST). Specifically, 500 women and men (BMI between 25-40 kg/m2) will be recruited from the Cedars-Sinai Medical Center network of hospitals and clinics. All participants will be enrolled in a 12-month weight-management program (WW, formerly Weight Watchers©) focusing on diet, physical activity and mindset skills, and randomized to one of four study arms: (1) WW only, (2) WW + modification of home food environment and online grocery delivery (AVOID), (3) WW + gamified inhibitory control training (RESIST), (4) WW + AVOID + RESIST. Baseline, 6- and 12-month assessments will be completed by experienced, English and Spanish speaking study staff. Aim 1 (Outcomes). (a) Tests how AVOID and RESIST affect weight loss and waist circumference (primary) and diet quality (secondary). H1a: AVOID and/or RESIST (arms 2, 3, 4) will result in greater weight loss at 6-month and 12-month timepoints compared to WW alone. (b) Tests potential ripple effects of AVOID and RESIST on available household members' diet quality (primary) and weight (secondary). H1b: The investigators predict that AVOID (arms 2 and 4) will produce greater dietary changes in household members than WW alone and RESIST (arms 1 and 3). Aim 2 (Mechanisms). Tests the mechanistic pathways of AVOID and RESIST by (a) comparing longitudinal changes in inhibitory control and home food environment across study arms; and (b) whether inhibitory control and the home food environment mediate the relationships between study arms and anthropometric and dietary outcomes. H2: AVOID will produce changes in the home food environment and RESIST will operate on inhibitory control. Aim 3 (Moderators). Examines how (a) individual characteristics (age, sex, ethnicity, socioeconomic status, household composition, physical activity, baseline BMI and executive functioning), and (b) process data (frequency of grocery delivery, dining out and take out, impulse control training and WW app use) moderate the relationship between study arms and anthropometric and dietary outcomes. These considerations are important to help explain heterogeneity in intervention outcomes and to understand who benefits from AVOID and/or RESIST.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Overweight

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
single-site, prospective, four-parallel-arm, randomized controlled trial
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
WW Only
Arm Type
Active Comparator
Arm Description
WW is commercially-available weight management program focusing on diet, physical activity and mindset skills.
Arm Title
WW + Home modification and grocery delivery (AVOID)
Arm Type
Experimental
Arm Description
WW + modification of home food environment + online grocery shopping and delivery
Arm Title
WW + Inhibitory control training (RESIST)
Arm Type
Experimental
Arm Description
WW + daily gamified inhibitory control training
Arm Title
WW + Home food modification and grocery delivery (AVOID) + Inhibitory control training (RESIST)
Arm Type
Experimental
Arm Description
WW + modification of home food environment + online grocery shopping and delivery + daily gamified inhibitory control training
Intervention Type
Behavioral
Intervention Name(s)
Home food environment and grocery delivery (AVOID)
Intervention Description
Participants (Arms 2 & 4) will receive 6 months of coaching (Zoom and/or email/text) to modify their home food environment and alter cues to promote healthy food choices
Intervention Type
Behavioral
Intervention Name(s)
Inhibitory control training (RESIST)
Intervention Description
Participants assigned to RESIST (Arms 3 & 4) will receive 6 months of coaching (Zoom and/or email/text) and gamified inhibitory control training.
Intervention Type
Behavioral
Intervention Name(s)
WW
Intervention Description
Participants assigned to all arms will receive 6 months of coaching (Zoom and/or email/text) and commercially-available weight management program focusing on diet, physical activity and mindset skills.
Primary Outcome Measure Information:
Title
Change in BMI from baseline to 12 months.
Description
BMI will be calculated by aggregating participants' self-reported height in meters and weight in kilograms at baseline, 6- and 12-months.
Time Frame
Baseline, 6-month, 12-month
Secondary Outcome Measure Information:
Title
Diet quality assessed by 24h-dietary recall
Description
Gold standard interviewer-administered, multi-pass 24h-recalls (2 weekdays, 1 weekend day) will be used to measure diet quality. The Nutrition Data System for Research software (Nutrition Coordinating Center, University of Minnesota) is used to analyze the data. Investigators will use the 24h-recalls to assess changes in participants and household members' overall diet quality, based on adherence to the dietary guidelines for fruits and vegetables, servings of whole grains, red/processed meat, alcoholic beverages and food/beverages with added sugars.
Time Frame
Baseline, 6-month, 12-month
Other Pre-specified Outcome Measures:
Title
Home availability of healthy and unhealthy foods and beverages
Description
Participants will self-report the availability of fruits and vegetables, servings of whole grains, red/processed meat, alcoholic beverages and food/beverages with added sugars in participants' homes. Responses will be scored as availability of healthy foods and beverages (e.g., fruits and vegetables), and availability of less healthy foods and beverages (e.g., processed meat, food/beverages with added sugars).
Time Frame
Baseline, 6-month, 12-month
Title
Flanker task
Description
Participants have 1000ms to identify which direction a central arrow is pointing. Participants complete 64 congruent and incongruent randomly mixed trials. In congruent trials flanking stimuli points in the same direction as the central stimulus while in incongruent trials flanking stimuli points in the opposite direction.
Time Frame
Baseline, 6-month, 12-month
Title
Continuous Performance Task Go/No-Go
Description
Participants respond to a target shape (e.g. a white five-pointed star) and withhold a response from non-target shapes. In 20% of presented trials an inhibitory response will be required.
Time Frame
Baseline, 6-month, 12-month
Title
Set-Shifting
Description
Participants categorize colored shapes by color or shape in three blocks. In the first two blocks, participants categorize shapes for 20 trials. In the third block, the categorization rules are randomly interleaved, and participants switch between rules. Participants have 1500ms to identify the stimulus and complete 96 trials with a 25% chance of rule-switching.
Time Frame
Baseline, 6-month, 12-month
Title
Demographics
Description
Participants will complete a questionnaire surveying: date of birth, sex, socioeconomic status (education level, household income, marital status, employment status), household composition (multigenerational, single, married, cohabitating, children) and race/ethnicity.
Time Frame
Baseline only
Title
Executive Functioning
Description
The Behavior Rating Inventory of Executive Function®- Adult Version (BRIEF-A) is a standardized measure of executive functions or self-regulation in everyday environment. The BRIEF-A assesses nine non-overlapping theoretically and empirically derived clinical scales: Inhibit, Self-Monitor, Plan/Organize, Shift, Initiate, Task Monitor, Emotional Control, Working Memory, and Organization of Materials. BRIEF-A is available in English and Spanish and can be computer-administered. Baseline score on the BRIEF will be tested as moderator of the relationships between study arms and outcomes.
Time Frame
Baseline, 6-month, 12-month
Title
WW Process Data
Description
Interactions such as tracked food, weight and activity in WW app will be passively recorded to operationalize engagement. A higher score indicates greater engagement.
Time Frame
monthly between baseline and 12-month
Title
Grocery Delivery Process data
Description
Frequency of grocery delivery and dining out/take out will be recorded through participants' self-report of grocery delivery. Higher frequencies of grocery delivery indicates greater engagement.
Time Frame
monthly between baseline and 12-month
Title
PolyRules! Process data
Description
Frequency/duration of gamified cognitive training will be passively recorded by the PolyRules! app. Greater frequency and duration indicate greater engagement.
Time Frame
monthly between baseline and 12-month
Title
Physical activity
Description
The International Physical Activity Questionnaire (IPAQ) will be used to assess activity in 5 domains: job-related; transportation; housework, house maintenance, and caring for family; recreation, sport, and leisure-time physical activity; and time spent sitting. Data conferred by the WW program will also be leveraged, as participants track their activity (type, duration and intensity) via the WW mobile app or online website. Investigators will examine how engagement in exercise and daily activities moderate the relationships between study arms and outcomes.
Time Frame
Baseline, 6-month, 12-month
Title
Eating attitudes
Description
The Dutch Eating Behavior Questionnaire (DEBQ) will be used to assess participants' approach to food and eating along three dimensions: emotional, external and restricted eating. There is a high degree of stability for each of these three eating behavior scales. Items on the DEBQ range from 1 (never) to 5 (very often), with higher scores indicating greater endorsement of the eating behavior.
Time Frame
Baseline, 6-month, 12-month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria (Main participants): Age 18 years or older BMI between 25-40 kg/m2 Read, write, and speak English with acceptable visual acuity Inclusion Criteria (Household participants): 14-years-old Parent consent for children <18-years-old Willingness to complete assessments / measurements Exclusion Criteria (Main participants): Currently enrolled in weight loss interventions or undergoing bariatric surgery Pregnant women Individuals for whom weight loss may be contraindicated (e.g., unstable coronary artery disease, end-stage disease, active cancer treatment, uncontrolled insulin-dependent diabetes, portal hypertension, drug/alcohol abuse) Individuals with severe cognitive delays or visual/hearing impairment Individuals who are unable or unwilling to complete the study assessments / measurements Exclusion Criteria (Household participants): ≤ 14-years-old Individuals who are unable or unwilling to complete the study assessments / measurements
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nenette Caceres, PhD
Phone
3104232062
Email
nenette.caceres@cshs.org
First Name & Middle Initial & Last Name or Official Title & Degree
Julissa Ruiz
Phone
3104232034
Email
julissa.ruiz@cshs.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah-Jeanne Salvy, PhD
Organizational Affiliation
Cedars-Sinai Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cedars-Sinai Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90069
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nenette Caceres, PhD
Email
nenette.caceres@cshs.org
First Name & Middle Initial & Last Name & Degree
Sarah J Salvy, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35798248
Citation
Caceres NA, Yu Q, Capaldi J, Diniz MA, Raynor H, Foster GD, Seitz AR, Salvy SJ. Evaluating environmental and inhibitory control strategies to improve outcomes in a widely available weight loss program. Contemp Clin Trials. 2022 Aug;119:106844. doi: 10.1016/j.cct.2022.106844. Epub 2022 Jul 5.
Results Reference
derived

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Avoid and Resist Strategies for Weight Management

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