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Effect of 100% Orange Juice on Food Intake and Glycemic Response in Adults

Effect of 100% Orange Juice Intake on Subjective Appetite, Food Intake, Glycemic Response and Subjective Mood in Healthy Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05012046
Enrollment
36
Registered
2021-08-19
Start date
2021-10-01
Completion date
2022-12-22
Last updated
2023-03-06

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

Conditions

Adult, Appetite, Glycemic Response, Healthy

Keywords

Food intake, Appetite, Blood glucose, Glycemic response, Orange juice, Adults

Brief summary

The purpose of this study is to determine the effects of 100% orange juice on short-term food intake (FI), satiety, post-prandial glycemia and mood in healthy adults. We hypothesize that the consumption of 100% orange juice in the pre-meal environment will improve satiety signals and mood, and suppress FI through its effect on post-prandial glycemia.

Detailed description

A randomized within-subjects repeated measures design will be employed. Study visits will take place in the morning, separated one-week apart. At each session, participants will consume one of three treatments: 1) 100% orange juice; 2) orange flavoured drink; or 3) water. Glycemic response will be measured for 60 minutes (baseline (0 minutes), 15 minutes, 30 minutes, 45 minutes and 60 minutes) post-treatment via finger prick. Blood glucose measures will also be provided over 24 hours via a Dexcom G6 continuous glucose monitoring (CGM) device. Subjective appetite, emotions and mood will be measured for 90 minutes min (baseline (0 minutes), 15 minutes, 30 minutes, 45 minutes, 60 minutes and 90 minutes) post-treatment. At 60 minutes, participants will consume an ad libitum pizza lunch to evaluate food intake. After lunch, participants will be sent home with a rest-of-the-day food intake sheet to record their snacks, meals, and beverages, as well as a physical activity log to record their physical activity for the rest of the day following test session completion.

Interventions

OTHEROrange juice

Matched for volume (240 mL/ 8 oz) of other test beverages. 100% orange juice.

OTHEROrange flavoured drink

Matched for volume (240 mL/ 8 oz) of other test beverages. Orange flavoured drink

OTHERWater

Matched for volume (240 mL/ 8 oz) of other test beverages. Water control

Sponsors

Toronto Metropolitan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* aged 18-45 years; * within the healthy body mass index (BMI) range for adults of 18.5-24.9 kg/m2.

Exclusion criteria

* individuals who are dieting; * restrained eaters; * breakfast skippers; * those who dislike breakfast or lunch treatment foods; * those taking medication; * individuals with any metabolic disorders or significant weight fluctuations.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline glycemic response (acute phase)Collected at baseline (0 minutes), 15 minutes, 30 minutes, 45 minutes, and 60 minutes post-treatment consumptionBlood glucose (mmol/L). Three drops of blood from the finger will be collected at each time point using a single-use, auto-disabling lancet device and sodium fluoride/potassium oxalate capillary blood collection tubes. Blood glucose will be measured using a YSI 2900D Biochemistry Analyzer (YSI Inc., Yellow Springs, OH).
Rest-of-day blood glucose concentrationsContinuous measurements for 24 hours post-treatment consumptionBlood glucose (mmol/L). Rest-of-day blood glucose concentrations will be determined using a Dexcom G6 CGM system.
Ad libitum food intakeAt 60 minutes post-treatment consumptionLunch pizza meal. Food intake will be determined by weighing the meal before and after serving. The net weight of the test meal will be converted to calories.

Secondary

MeasureTime frameDescription
Change from baseline subjective appetiteCollected at baseline (0 minutes), 15 minutes, 30 minutes, 45 minutes, and 60 minutes post-treatment consumptionMeasured using visual analogue scales (VAS). Each VAS is a 100 mm line where they will place a pencil mark to describe their feelings. Questions will include desire to eat, fullness, hunger, and prospective food consumption. Individual questions will be used to form a composite score.
Rest-of-the-day physical activityFor the rest of the day following test session completion (1 day)Participants will be sent home with a rest-of-the-day physical activity recall sheet to record any activities performed. Physical activity questionnaire
Change from baseline subjective emotions and moodCollected at baseline (0 minutes), 15 minutes, 30 minutes, 45 minutes, and 60 minutes post-treatment consumptionMeasured using visual analogue scales. Each VAS is a 100 mm line where they will place a pencil mark to describe their feelings. Questions will measure aggression, anger, excitement, disappointment, frustration, alertness, sadness, tension, effort, happiness, weariness, calmness, sleepiness, and wellness. Individual questions will be used to form a composite score.
Rest-of-the-day food intakeFor the rest of the day following test session completion (1 day)Participants will be sent home with a rest-of-the-day food intake recall sheet to record their snacks, meals, and beverages. Rest of day food log

Countries

Canada

Outcome results

None listed

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