Targeted Food Incentives to Improve Diet Quality and Health Among Adults (Smartcart)

September 30, 2021 updated by: University of Rhode Island

Individually-targeted Incentives, Diet Quality, and Health Outcomes Among Adults

The purpose of this study is to test whether individual-level targeted price incentives for healthier foods can improve the diet quality of grocery purchases made by adults in comparison to a "one size fits all" approach. To test this, the investigators plan to implement a 8-month randomized controlled cross-over trial. The intervention group will receive a small discount for using their loyalty card and weekly coupons for healthier foods (e.g. fruits, vegetables, whole grains, lean meats and seafood, low-fat dairy) that are selected based on the individual's past purchase history, dietary preferences, their baseline diet quality, and their estimated likelihood of using the coupon. Individualized coupons will be automatically sent to customers' loyalty cards each week, and separate emails with appropriate nutrition education and information about the coupons will be sent to participants weekly. The control group will receive a small discount for using their loyalty cards during the first phase of the study (3-months), occasional untargeted coupons, and weekly emails with untargeted nutrition education. Following phase1, there will be a 2-month washout period, and then the intervention and control groups will cross over for the remaining 3-months of the study. The investigators will collect purchase data from all participants as well as food frequency questionnaires and other self-reported behavioral and health questions at baseline, after phase 1 completion, and after phase 2 completion. The investigators hypothesize that participants in the intervention group will meaningfully improve the overall quality of their food purchases (measured using the Grocery Purchase Quality Index-2016) as well as their overall diet quality (measured using the Healthy Eating Index 2010.

Study Overview

Detailed Description

A detailed description of Eligibility and outcome measures is entered elsewhere

Study Type

Interventional

Enrollment (Actual)

224

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Rhode Island
      • Kingston, Rhode Island, United States, 02881
        • University of Rhode Island

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18 years or older
  • Speaks English
  • Non-store employee
  • Primary shopper in the household
  • Purchases at least half of weekly groceries at supermarket
  • Not pregnant or planning on becoming pregnant before April 2019

Exclusion Criteria:

  • Younger than 18 years of age
  • Does not speak English
  • Employee at supermarket
  • Pregnant or planning to become pregnant before April 2019
  • Not primary shopper for household
  • Purchases less than half of weekly groceries at supermarket

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Targeted incentives arm
The interventions received by the experimental group include: 1) weekly emails with targeted coupons for healthier products, 2) weekly emails with targeted nutrition education, and 3) and a nominal discount on grocery purchases for using their loyalty card
Participants receiving individually-targeted incentives will receive weekly coupons for healthier foods that are informed by their purchase history, responses to behavioral and health questions, food preferences, and need for improvement in different categories
All participants will receive a nominal discount on all groceries for using their loyalty card and nutrition education through weekly emails.
ACTIVE_COMPARATOR: Usual care arm
The interventions included under "usual care" include 1) untargeted nutrition education, 2) occasional untargeted coupons for healthier products, and 3) a nominal discount on their grocery purchases for using their loyalty card. These interventions are only received by participants randomized to the usual care arm (rather than the entire population of shoppers), and will allow for testing whether targeting discounts and nutrition education improves the diet quality of purchases in comparison to untargeted approaches.
All participants will receive a nominal discount on all groceries for using their loyalty card and nutrition education through weekly emails.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Likelihood of purchasing targeted products
Time Frame: 3- 6- and 9-month changes within and between the intervention and control groups
Within produce, whole grain cereals & breads, lean meats, low-fat dairy, and beverages, will look at the proportion of expenditures (i.e. percent of dollars) in those categories before and after the intervention between treatment and control group.
3- 6- and 9-month changes within and between the intervention and control groups
Grocery Purchase Quality Index (GPQI) 2016
Time Frame: 3, 6- and 9-month changes in the GPQI-16 and its components within and between the intervention and control groups

The GPQI is a validated measure for scoring the quality of household grocery purchases by comparing the percent spent within different food categories with recommended spending.

https://utah.pure.elsevier.com/en/publications/the-grocery-purchase-quality-index-2016-an-innovative-approach-to

3, 6- and 9-month changes in the GPQI-16 and its components within and between the intervention and control groups

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Healthy Eating Index (HEI) -2010 for the primary shopper
Time Frame: 3, 6- and 9-month changes in the HEI-10 and its components within and between the intervention and control groups

The HEI-10 is a validated measure of individual-level diet quality that measures compliance with US Dietary recommendations.

https://www.ncbi.nlm.nih.gov/pubmed/24453128

3, 6- and 9-month changes in the HEI-10 and its components within and between the intervention and control groups
Percent expenditures within targeted categories
Time Frame: 3, 6- and 9-month changes in percent spending in targeted categories within and between the intervention and control groups
The investigators will compute the percent of shopping dollars people spend in fruits, vegetables, whole grains, dairy, lean meat, and seafood.
3, 6- and 9-month changes in percent spending in targeted categories within and between the intervention and control groups
Self-reported height and weight used to compute body mass index (BMI)
Time Frame: 3, 6- and 9-month changes in BMI
The investigators will compute body mass index from self-reported weight in pounds and height in inches (weight (lbs) * 703/height (in)/height (in)
3, 6- and 9-month changes in BMI

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported food neophobia as an effect modifier on the primary and secondary outcomes
Time Frame: Baseline and 9-months
The investigators will examine whether food neophobia modifies the effect of the intervention on the primary and secondary outcomes. Food neophobia was measured via 8 self-reported questions with a 5-point Likert scale ranging from completely disagree to completely agree. Responses will be summed, and higher scores reflect greater variety-seeking in eating experiences (i.e. less neophobia). We will test for an interaction between this continuous measure and the intervention on specified primary and secondary outcomes
Baseline and 9-months
Self-reported food literacy as an effect modifier on the primary and secondary outcomes
Time Frame: Baseline
The investigators will examine whether food literacy modifies the effect of the intervention on the primary and secondary outcomes. Food literacy was measured using a 12-item questionnaire, with 4- and 5-point Likert type scales, with higher scores indicating greater food literacy.
Baseline
Coupon proneness as an effect modifier on the primary and secondary outcomes
Time Frame: Baseline and 9-months
The investigators will examine whether coupon proneness modifies the effect of the intervention on the primary and secondary outcomes. Coupon proneness was measured via a 22-item self-reported questionnaire with 7-point Likert scales. Higher scores indicate greater likelihood of using coupons.
Baseline and 9-months
Nutritional self-efficacy as a modifier on the primary and secondary outcomes
Time Frame: Baseline
The investigators will examine whether nutritional self-efficacy modifies the effect of the intervention on the primary and secondary outcomes. Nutrition self-efficacy was measured via self-report using a 5-item scale with Likert responses (range 0-3) with higher scores indicating greater self-efficacy in nutritional domains.
Baseline
Food security as a modifier on the primary and secondary outcomes
Time Frame: Baseline and 9-months
The investigators will examine whether food security modifies the effect of the intervention on the primary and secondary outcomes. Household food security was assessed via a 6-item short form, with higher scores indicating greater food insecurity.
Baseline and 9-months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Maya Vadiveloo, University of Rhode Island

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

September 10, 2018

Primary Completion (ACTUAL)

May 1, 2019

Study Completion (ACTUAL)

May 1, 2019

Study Registration Dates

First Submitted

July 18, 2018

First Submitted That Met QC Criteria

November 16, 2018

First Posted (ACTUAL)

November 20, 2018

Study Record Updates

Last Update Posted (ACTUAL)

October 1, 2021

Last Update Submitted That Met QC Criteria

September 30, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 1240194-3
  • AWD05956 , Project 0006418 (OTHER_GRANT: Foundation for Food and Agricultural Research)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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