Multi-level Supermarket Discount Study

NCT ID: NCT04178824

Last Updated: 2024-10-02

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

167 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-09-01

Study Completion Date

2022-11-15

Brief Summary

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The study team's objective is to test the effect of supermarket discount levels on fruit and vegetable (F\&V) and non-caloric beverage purchasing and consumption, as well as health outcomes. The study team will implement this economic intervention in a local supermarket chain to assess the effects of a 32-week intervention of fruit and vegetable (F\&V) and non-caloric beverage discounts of 30%, 15%, and 0% (control group) on purchasing, dietary intake, and health outcomes, including body weight and composition, blood pressure, and biochemical markers of cardiovascular disease risk. The 32-week intervention will be preceded by an 8-week baseline and will have a follow-up period of 16 weeks. There will be no discounts in effect during the baseline and follow-up periods.

Detailed Description

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The objective is to test the effect of supermarket discount levels on fruit and vegetable (F\&V) and non-caloric beverage purchasing and consumption, as well as health outcomes. The study team will implement this economic intervention in a local supermarket chain to assess the effects of a 32-week intervention of fruit and vegetable (F\&V) and non-caloric beverage discounts of 30%, 15%, and 0% (control group) on purchasing, dietary intake, and health outcomes, including body weight and composition, blood pressure, and biochemical markers of cardiovascular disease risk. The prediction is that the impact will increase with the level of discount. The 32-week intervention will be preceded by an 8-week baseline and will have a follow-up period of 16 weeks. There will be no discounts in effect during the baseline and follow-up periods. The prediction is that some of the interventional effects will carry over to the follow-up period.

Conditions

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Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Experimental 15% discount intervention

15% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets

Group Type EXPERIMENTAL

Discount Intervention

Intervention Type BEHAVIORAL

15% or 30% discount on fruits and vegetables

Experimental 30% discount intervention

30% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets

Group Type EXPERIMENTAL

Discount Intervention

Intervention Type BEHAVIORAL

15% or 30% discount on fruits and vegetables

No intervention control group

0% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Discount Intervention

15% or 30% discount on fruits and vegetables

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* BMI: 24.5 - 50
* Weight Stable (±5% body weight in last 3 mo)
* Accessible by telephone
* Living in NYC and not planning move
* Primary household food shopper
* ≥50% of food shopping at Foodtown/Brooklyn Harvest and agrees to 100% shopping at store during study
* Consumption of \>50% of food shopping
* Eat out or take out ≤5 times weekly

Exclusion Criteria

* Pregnant or contemplating pregnancy
* Enrolled in related studies
* Active weight loss program
* Presence of serious medical (e.g. cancer, diabetes) or psychiatric disease (e.g. bipolar)
* Changes in medications or smoking in past 3 mo
* Excessive alcohol use (≥4 drinks/day) or illicit drug use
* Planning a vacation ≥ 4 consecutive weeks or 6 total weeks during study
* Receiving SNAP benefits
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role collaborator

Icahn School of Medicine at Mount Sinai

OTHER

Sponsor Role lead

Responsible Party

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Allan Geliebter

Professor, Department of Psychiatry

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Allan Geliebter, PhD

Role: PRINCIPAL_INVESTIGATOR

Icahn School of Medicine at Mount Sinai

Locations

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Mount Sinai St. Luke's

New York, New York, United States

Site Status

Countries

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United States

References

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Nzesi A, Roychowdhury L, De Jesus ML, Brown A, Geliebter A. Body weight, dietary intake, and health risk factors pre-COVID and during the COVID-19 pandemic. Appetite. 2022 Nov 1;178:106182. doi: 10.1016/j.appet.2022.106182. Epub 2022 Aug 6.

Reference Type RESULT
PMID: 35940334 (View on PubMed)

Poskute AS, Nzesi A, Geliebter A. Changes in food intake during the COVID-19 pandemic in New York City. Appetite. 2021 Aug 1;163:105191. doi: 10.1016/j.appet.2021.105191. Epub 2021 Mar 3.

Reference Type RESULT
PMID: 33667497 (View on PubMed)

Nzesi A, Owusu B, Barry J, Sandhu M, Geliebter A. Impact of a randomized controlled trial of discounts on fruits, vegetables, and noncaloric beverages in NYC supermarkets on food intake and health risk factors. PLoS One. 2023 Nov 22;18(11):e0291770. doi: 10.1371/journal.pone.0291770. eCollection 2023.

Reference Type RESULT
PMID: 37992046 (View on PubMed)

Poskute AS, Ang IYH, Rahman N, Geliebter A. Effects of discounting fruits, vegetables, and noncaloric beverages in New York City supermarkets on purchasing, intake, and weight. Obesity (Silver Spring). 2024 Jul;32(7):1290-1301. doi: 10.1002/oby.24058.

Reference Type RESULT
PMID: 38932711 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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R01DK105440

Identifier Type: NIH

Identifier Source: secondary_id

View Link

GCO 16-1050

Identifier Type: -

Identifier Source: org_study_id

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