"Make It Fresh, For Less" Supermarket Pilot Study

November 8, 2017 updated by: Eric B. Rimm, Harvard School of Public Health (HSPH)
The purpose of this study is to examine the impact of environmental modifications (choice architecture and a marketing campaign) in combination with weekly text messages on purchases of foods made by parents shopping in a large supermarket.

Study Overview

Detailed Description

The "Make It Fresh, For Less" Supermarket Pilot Study is a supermarket-based intervention developed by the Harvard T.H. Chan School of Public Health in collaboration with the nonprofit organization ChopChop Magazine (chopchopmagazine.org) and a large Northeastern supermarket chain. A promotional campaign advertising low-cost, kid-friendly meals was piloted in one store selected by the supermarket partner, with promotions rotating every 4 weeks during a 16-week intervention period. Parent shoppers were recruited (n=401) at the store and given a study loyalty card to track their transactions. At the start of the intervention, half of the participants were additionally randomized to receive weekly behavioral messages via text message or email. Supermarket purchases were assessed at baseline, during the 16-week intervention, and up to 6-weeks post-intervention.

Primary Aim 1: to examine the impact of a choice architecture intervention in combination with a promotional campaign on food purchases of parents shopping in a large supermarket. It is hypothesized that there will be an increase in selection of foods targeted by the promotional campaign when physical modifications are made.

Primary Aim 2: to examine the impact of weekly behavioral messages in combination with an environmental change intervention on food purchases of parents shopping in a large supermarket. It is hypothesized that there will be a greater increase in selection of foods targeted by the promotional campaign among participants receiving the messages compared to participants exposed to the environmental change intervention alone.

Study Type

Interventional

Enrollment (Actual)

401

Phase

  • Not Applicable

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18 years of age or older
  • English-speaking
  • Live with a child 18 years of age or younger
  • Do more than 50% of shopping at the study store
  • Primary shopper in the household

Exclusion Criteria:

  • None

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: environmental change
Shoppers were exposed to modifications to the supermarket environment to encourage selection of low-cost, kid-friendly meals
  1. Offer kid-friendly, low-cost recipes in a prominent, high-traffic location.
  2. Offer healthy default ingredients (bundled ingredients promoted with recipes).
  3. Promote recipe ingredients with prominently displayed signage and images.
  4. Promote recipes in multiple locations throughout the store.
Other Names:
  • choice architecture
  • promotional campaign
Experimental: environmental change and messaging
Shoppers were exposed to modifications to the supermarket environment and weekly messages via text or email to encourage selection of low-cost, kid-friendly meals
  1. Offer kid-friendly, low-cost recipes in a prominent, high-traffic location.
  2. Offer healthy default ingredients (bundled ingredients promoted with recipes).
  3. Promote recipe ingredients with prominently displayed signage and images.
  4. Promote recipes in multiple locations throughout the store.
Other Names:
  • choice architecture
  • promotional campaign
Short, behavioral messages sent to participants via text message or email each week to promote the in-store environmental changes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in weekly purchases of recipe components (Selection of items bundled with each recipe) during four, 4-week promotional campaigns
Time Frame: Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Purchase of recipe ingredients
Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in weekly purchases of other food categories (substitution of recipe ingredients for other foods)
Time Frame: Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Substitution of recipe ingredients for other foods
Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Differential change in weekly purchases of recipe components by SNAP-eligibility
Time Frame: Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Stratification by SNAP-eligibility, recipe components
Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Differential change in weekly purchases of other food groups (substitution) by SNAP-eligibility
Time Frame: Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Stratification by SNAP-eligibility, other food groups
Baseline, during intervention (4 weeks each) and up to 6 weeks post-intervention
Acceptability of intervention (self-reported survey measures)
Time Frame: Up to 6 weeks post-intervention
Shopper responses to survey questions asking participants to rate the acceptability of each recipe (taste, cost, difficulty, perceptions of children's preferences) on a Likert scale from 1-5.
Up to 6 weeks post-intervention
Recall of intervention (self-reported survey measures)
Time Frame: Up to 6 weeks post-intervention
Shopper responses to survey questions regarding aided and unaided recall. Unaided recall asks shoppers to choose the best description of what they saw in the store and aided recall asks shoppers whether they remember seeing various elements of the display in the store (yes, no, not sure). These measures will be combined to report the proportion of shoppers who recalled each component of the intervention either through aided or unaided means.
Up to 6 weeks post-intervention
Adoption of intervention (self-reported survey measures)
Time Frame: Up to 6 weeks post-intervention
Shopper responses to survey questions asking whether the shopper made each recipe in the display.
Up to 6 weeks post-intervention
Reach of intervention (direct observation measures)
Time Frame: During intervention (4 weeks each)
Observation of shopper interactions with promotional campaign (count of number of shoppers who passed the display, looked at the display, and took an item from the display).
During intervention (4 weeks each)
Fidelity to intended intervention (direct observation measures)
Time Frame: During intervention (4 weeks each)
Monthly random site visits to assess presence or absence of each element of the display (placards, poster, recipe cards, intended ingredients, store banners).
During intervention (4 weeks each)

Collaborators and Investigators

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

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)

October 8, 2015

Primary Completion (Actual)

January 1, 2017

Study Completion (Actual)

January 1, 2017

Study Registration Dates

First Submitted

February 8, 2017

First Submitted That Met QC Criteria

November 8, 2017

First Posted (Actual)

November 13, 2017

Study Record Updates

Last Update Posted (Actual)

November 13, 2017

Last Update Submitted That Met QC Criteria

November 8, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • BECR-111191

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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