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Multi-level Supermarket Discount Study

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Mount Sinai Health System

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Discount Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04178824
GCO 16-1050
R01DK105440 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full description

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.

Enrollment

167 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

167 participants in 3 patient groups

Experimental 15% discount intervention
Experimental group
Description:
15% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets
Treatment:
Behavioral: Discount Intervention
Experimental 30% discount intervention
Experimental group
Description:
30% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets
Treatment:
Behavioral: Discount Intervention
No intervention control group
No Intervention group
Description:
0% discount on fruits, vegetables and non-caloric beverages at the designated supermarkets

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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