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Healthy Online Grocery Defaults for Obesity Prevention (FGS Trial)
N/A
Recruiting
Led By Stephanie Anzman-Frasca, PhD
Research Sponsored by State University of New York at Buffalo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (weeks 1 and 2) and intervention (weeks 3 and 4)
Awards & highlights
Summary
This trial aims to help prevent childhood obesity by using pre-filled online grocery carts to help families shop more healthily.
Who is the study for?
This trial is for families with a child aged 2-5, where the parent/guardian is obese (BMI >30) and shops online at Tops/Aldi stores most of the time. The parent must be over 18 and speak English. It aims to help these families make healthier grocery choices.
What is being tested?
The study tests if using pre-filled, healthier default options in online grocery shopping carts can encourage better food choices among families with young children at risk of obesity, potentially improving their home diet.
What are the potential side effects?
Since this intervention involves changing shopping habits rather than medical or drug treatments, there are no direct side effects like those associated with medications. However, changes in diet may affect individual family members differently.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (weeks 1 and 2) and intervention (weeks 3 and 4)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (weeks 1 and 2) and intervention (weeks 3 and 4)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Cost of Groceries
Change in Energy Purchased
Change in Nutritional Quality of Purchases
+6 moreSecondary study objectives
Meals and Meal Intake of Child
Meals and Meal Intake of Parent
Nutritional Quality of Child's Intake
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Group 2 - DefaultExperimental Treatment1 Intervention
Participants will receive healthy recipes (3 main meal + 1 snack/breakfast/lunch recipe per week of the two-week intervention). In addition, in this group, participants' online grocery shopping carts will be pre-filled with ingredients corresponding to the provided recipes. They will be told that their cart has been filled with items that can be used to make recipes from the provided recipe cards, and that they can modify it as they like.
Group II: Group 1 - RecipesActive Control1 Intervention
Participants will receive healthy recipes (3 main meal + 1 snack/breakfast/lunch recipe per week of the two-week intervention).
Find a Location
Who is running the clinical trial?
State University of New York at BuffaloLead Sponsor
264 Previous Clinical Trials
52,030 Total Patients Enrolled
18 Trials studying Obesity
9,877 Patients Enrolled for Obesity
Stephanie Anzman-Frasca, PhDPrincipal InvestigatorUniversity at Buffalo
3 Previous Clinical Trials
1,013 Total Patients Enrolled
1 Trials studying Obesity
50 Patients Enrolled for Obesity
Mackenzie J Ferrante, PhDPrincipal InvestigatorUniversity at Buffalo
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not primarily shop online at Tops or Aldi.I am a parent/guardian over 18 participating in the trial.I have a child aged between 2 to 5 years.My parent or guardian is younger than 18.One of my parents is obese (BMI over 30).
Research Study Groups:
This trial has the following groups:- Group 1: Group 1 - Recipes
- Group 2: Group 2 - Default
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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