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How healthy adults determine food portion sizes

The effects of food cue manipulations on pre-meal planning and actual food intake in healthy adults

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613001019796
Enrollment
35
Registered
2013-09-12
Start date
2013-10-31
Completion date
2014-08-11
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study will provide useful data on the importance of three sensory characteristics possibly used by humans in meal planning. Knowledge in this area will then be incorporated as part of the overweight and obesity treatment, or in the prevention of weight gain. We hypothesize that visual, olfactory, and food form cues are important determinants of expected satiation and food portion size selection.

Interventions

Study design: Randomized, controlled, crossover design Test foods: 1. Visual manipulations a. Visible fat – energy-matched butter on toasted French bread b. Visible sugar – energy-matched jam on toasted French bread c. Visible protein – energy-matched ham on toasted French bread d. Visible protein – energy-matched cream cheese on toasted French bread 2. Olfactory manipulations a. Natural odour – plain mashed potato with Italian herbs b. “Fat” odour – herbs + butter or bacon essence added to m

Study design: Randomized, controlled, crossover design Test foods: 1. Visual manipulations a. Visible fat – energy-matched butter on toasted French bread b. Visible sugar – energy-matched jam on toasted French bread c. Visible protein – energy-matched ham on toasted French bread d. Visible protein – energy-matched cream cheese on toasted French bread 2. Olfactory manipulations a. Natural odour – plain mashed potato with Italian herbs b. “Fat” odour – herbs + butter or bacon essence added to mashed potato 3. Food form manipulations a. Solid – apple b. Liquid – apple juice Participants will be screened at baseline to confirm eligibility and baseline measurements will be obtained. If qualified, participants will attend eight 45-minute sessions to undergo all study conditions in a random order. Participants will be asked to avoid vigorous activity and drinking alcohol on the previous day, and fast for 10 – 12 hours prior to each session. Participants will arrive at the laboratory between 8am and 9am, and overnight fasting will be verbally confirmed by the researcher. Upon arrival, participants will be asked to drink 200ml of plain water (as a control for thirst and baseline hunger), and baseline appetite ratings will be assessed using validated visual analog scales (VAS) (Flint 2000) 5 minutes after water consumption. Test foods will be presented in large portion sizes (to avoid portion bias and to prevent plate-cleaning), and participants will be asked to take a portion of the test food that is expected to help them achieve a fullness level of 8 out of 10. Participants will also be asked to rate the appearance and intensity of smell of foods. Following that, the portioned food will be removed, and an identical plate of food will be presented to participants again. They will be given 30 minutes to consume the same food until a fullness level of 8 is achieved. After 30 minutes, participants will be asked to rate the palatability of the test foods, how often they will consume the same food again, and VAS again before leaving the lab. Participants will return until all conditions are completed. The washout period between study visits will be at least 24 hours.

Sponsors

University of South Australia
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Males and females * Age 18-60 years * BMI 18.5 – 35 kgm-2 * Not taking medications that affect metabolism or appetite * Non-smokers * Are familiar with test foods * Willing to comply to study protocol

Exclusion criteria

* Presence of disease(s) * Food allergies or intolerance

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026