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Increasing Availability of Lower Energy Meals on Food Choice and Intake

Socioeconomic Position and the Impact of Increasing the Proportion of Lower Energy Foods Available on Supermarket Meal Choices and Consumption

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04893213
Enrollment
80
Registered
2021-05-19
Start date
2021-04-13
Completion date
2021-07-05
Last updated
2022-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diet, Healthy, Eating Behavior, Food Selection, Obesity

Keywords

availability, socio-economic position, food choice, eating behaviour

Brief summary

This study will examine the effectiveness of a structural intervention (baseline proportion of lower energy ready meals vs increased proportion of lower energy ready meals) on calories (kcal) ordered and consumed. The study will use a within-subjects design, meaning all participants will be exposed to both conditions (baseline vs increased lower energy meal menus). The procedure will involve participants placing orders for supermarket ready meals, which are then delivered to their homes for their consumption. This study will also investigate whether the effectiveness of the intervention varies, depending on socioeconomic position (SEP). The primary hypothesis is that increasing proportion of lower energy options will decrease total kcal ordered and consumed, and that there will be no difference between higher and lower SEP. To address the limited evidence on longer term impacts of dietary interventions on daily energy intake, the present study will also examine post-meal energy consumption up to midnight on the following day. Finally, this study will explore the psychological processes that might underlie the effectiveness of the intervention among individuals with higher and lower SEP; namely, food choice motives, satiety responsiveness, plate clearing tendencies, and food waste concerns.

Detailed description

See attached protocol documents.

Interventions

OTHERManipulation of availability of lower energy meal options

Menus provided differ in % of menu options that are higher vs. lower in energy

Sponsors

University of Liverpool
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* UK (United Kingdom) residents, aged 18 or over * Fluent in English * Have access to a phone/tablet/computer device which has access to Internet and a functioning camera * Willing to consume two supermarket ready meals * Have access to a functioning microwave and oven for the preparation of the ready meals

Exclusion criteria

* Taking part more than once * Another member of the same household has participated in the study (Multiple members of the same household will not be allowed to take part) * Current or historic diagnosed eating disorders * Currently on any medication which affects appetite * Any of the following dietary restrictions, intolerances, or allergies (Vegetarian, vegan, gluten-free, sugar-free, dairy/lactose-free, food allergy - such as milk, eggs, nut, wheat, fish, etc) * History of severe childhood allergies, anaphylaxis or anaphylactic shock

Design outcomes

Primary

MeasureTime frameDescription
Total meal energy (kcal) ordered20 minutes (the time frame denotes time taken to complete the initial study questionnaire and make the food choices)Calculated as the sum of the kcal content of the main and side ordered
Total meal energy (kcal) consumedOnce the food has been delivered, the time frame is up to 72 hoursCalculated as the sum of the kcals consumed from the main and side combined

Secondary

MeasureTime frameDescription
Post-meal intake (kcal)Measured 24-30 hours after study meal is consumedCalculated as total energy (kcal) consumed after the study meal until midnight on the following day (dietary recall).

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026