SEP and the Impact of Portion Size on Daily Energy Intake

Sponsor
University of Liverpool (Other)
Overall Status
Recruiting
CT.gov ID
NCT05173376
Collaborator
European Research Council (Other)
60
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2
8.4
7.1

Study Details

Study Description

Brief Summary

Reducing food portion size is a potential strategy to reduce energy intake. There is some evidence to suggest that individuals with lower socioeconomic position (SEP) intend to eat more from larger portions, suggesting that the effect of portion size on food intake might vary by SEP. However, no study has tested this by measuring actual food intake. This study examines whether reductions to the portion size of components of a main meal will reduce daily energy intake, and whether and how socioeconomic position (higher vs lower) moderates the portion size effect.

In a crossover experiment, participants will be served all meals in the lab on two separate days, with the portion size of main meal components at lunch and dinner manipulated (i.e. smaller on one day vs larger on the other day). All other foods offered are identical. Food intake from the portion-manipulated lunch and dinner, as well as all other meal components (breakfast, dessert, seconds, snacks) will be measured, and any additional food consumed by the participant will be measured using self-report, giving total daily energy intake (kcal).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Portion size manipulation
N/A

Detailed Description

See attached protocol document.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Socioeconomic Position and the Effect of Portion Size Reduction: a 1-day Dietary Behaviour Experimental Study
Actual Study Start Date :
Oct 25, 2021
Anticipated Primary Completion Date :
May 8, 2022
Anticipated Study Completion Date :
Jul 8, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Larger portions

the main meal component (lunch/dinner) served to participants in the laboratory, reflecting 100% portion. All other foods are identical across conditions (e.g. sides, seconds, breakfast, dessert, snacks).

Behavioral: Portion size manipulation
The intervention was administered via changing portion sizes of foods served to participants.

Experimental: Smaller portions

the main meal component (lunch/dinner) served to participants in the laboratory, reflecting 66% portion (i.e. reduced portion size). All other foods are identical across conditions (e.g. sides, seconds, breakfast, dessert, snacks).

Behavioral: Portion size manipulation
The intervention was administered via changing portion sizes of foods served to participants.

Outcome Measures

Primary Outcome Measures

  1. Daily energy intake [24 hours after intervention administered]

    Total energy (kcal) consumed from breakfast, lunch, dinner, dessert, snackbox, and any self-reported additional foods.

Secondary Outcome Measures

  1. Appetite [24 hours after intervention administered]

    Hunger and fullness sensations before and after laboratory-based meals (self-reported on visual analogue scales anchored at 0 'Not at all' and 100 'Extremely')

  2. Moderate-vigorous physical activity [24 hours after intervention administered]

    Moderate-vigorous physical activity (recorded using wearable activity tracker), operationalised as active minutes/day (logged for activities with a metabolic equivalent of >/3)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Female

  • UK (United Kingdom) residents, aged 18 or over

  • Fluent in English

  • willing to consume the test foods

  • Self report liking of test foods

  • BMI between 22.5 - 32.5kg2

Exclusion Criteria:
  • taking medication which affects appetite

  • currently pregnant

  • history of eating disorders

  • currently on a diet to lose weight

  • food allergies, intolerances or specific dietary requirements (including being vegetarian or vegan)

  • participated in 2018 Mood Study

  • currently participating in another study where meals are provided

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Liverpool Liverpool United Kingdom L69 7ZA

Sponsors and Collaborators

  • University of Liverpool
  • European Research Council

Investigators

  • Principal Investigator: Eric Robinson, PhD, Study Principle Investigator

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Eric Robinson, Principal Investigator (Reader in Psychological Sciences), University of Liverpool
ClinicalTrials.gov Identifier:
NCT05173376
Other Study ID Numbers:
  • 803194
First Posted:
Dec 29, 2021
Last Update Posted:
Dec 29, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eric Robinson, Principal Investigator (Reader in Psychological Sciences), University of Liverpool

Study Results

No Results Posted as of Dec 29, 2021