The Relationship Between Blood Glucose and Satiety Ratings

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-01

Study Completion Date

2020-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Participants will be given a drink (and no drink for one of the treatments) prior to a pizza dinner. Ratings on satiety, appetite and desire to eat will be asked with the use of a questionnaire. Blood glucose will also be measured. One hour after the drink, participants will be given a pizza and can eat as much as they want. The pizza remaining will be weighed.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Solutions for Hunger and Regulating Eating

NCT05004883

Overweight and Obesity

ACTIVE_NOT_RECRUITING NA

Hunger, Satiety, and Metabolic Responses to High-fat Meals of Varying Fatty Acid Composition

NCT02966444

Body Weight Changes

UNKNOWN NA

Does Meal Replacement With a Carbohydrates and Protein Supplement Induce Weight Loss in Overweight and/or Obese Adults?

NCT04458493

Weight Loss

UNKNOWN NA

Integral Physiological Adaptations to Carbohydrate Periodization

NCT05464342

Sleepiness Fatigue Feeding Patterns +1 more

COMPLETED NA

Neural Mechanisms for Appetitive Responses to High Reward Foods

NCT02945475

Appetitive Behavior Obesity

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Each participant will receive all three treatments on separate occasions in random order (separated by a week). The three treatments include control (no supplement), carbohydrates - protein (Generation UCAN supplement, 250ml, 10% solution) and carbohydrates alone (Mirexus PhytoSpherix, 250ml, 10% solution). Participants will report to the lab between 4-5 pm and 4 hours after their last meal on day they have not exercised. Participants will record food intake the day of the first experiment and will be asked to replicate both type and quantity for subsequent visits. Upon arrival at the lab, baseline measures (blood glucose as well as rating of satiety ratings, appetite and desire to eat (10-point visual analogue scale). Then the treatment will be given and all the aforementioned variables will be remeasured at 15, 30, 45 and 60 minutes post drink. At 65 minutes, participants will be provided with an ad libitum pizza meal. Participants will be told to eat until they are "comfortably full" (Bellissimo et al., 2008). The pizza provided will be weighed initially and once the participant is done eating and has left the lab, the remaining pizza will be weighed and recorded. The pizza will be a cheese only pizza to minimize any difference in energy intake due to the location of additional items placed on the pizza.

Participants will not be told the true purpose of this experiment, instead they will be told that the pizza meal is a reward for participating in the study. Later, at the conclusion of the study all will be debriefed.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Satiety Appetite

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

control

no supplement will be provided on the day of the experiment

Group Type EXPERIMENTAL

satiety ratings

Intervention Type BEHAVIORAL

questionnaire on satiety ratings will be provided to participants 15, 30, 45 and 60 min after the drink (or no drink)

Generation UCAN

carbohydrates - protein (Generation UCAN supplement, 250ml, 10% solution)

Group Type EXPERIMENTAL

Generation UCAN supplementation

Intervention Type DIETARY_SUPPLEMENT

carbohydrates - protein (Generation UCAN supplement, 250ml, 10% solution)

satiety ratings

Intervention Type BEHAVIORAL

questionnaire on satiety ratings will be provided to participants 15, 30, 45 and 60 min after the drink (or no drink)

Mirexus PhytoSpherix

carbohydrates alone (Mirexus PhytoSpherix, 250ml, 10% solution)

Group Type EXPERIMENTAL

Mirexus PhytoSpherix supplementation

Intervention Type DIETARY_SUPPLEMENT

carbohydrates alone (Mirexus PhytoSpherix, 250ml, 10% solution)

satiety ratings

Intervention Type BEHAVIORAL

questionnaire on satiety ratings will be provided to participants 15, 30, 45 and 60 min after the drink (or no drink)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Generation UCAN supplementation

carbohydrates - protein (Generation UCAN supplement, 250ml, 10% solution)

Intervention Type DIETARY_SUPPLEMENT

Mirexus PhytoSpherix supplementation

carbohydrates alone (Mirexus PhytoSpherix, 250ml, 10% solution)

Intervention Type DIETARY_SUPPLEMENT

satiety ratings

questionnaire on satiety ratings will be provided to participants 15, 30, 45 and 60 min after the drink (or no drink)

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Healthy males and females at the age of 18-40
* sedentary individuals

Exclusion Criteria

* exercise more than twice per week
* does not like pizza
* do not eat three meals a day
* medications that affect eating patterns
* have metabolic and gastrointestinal diseases

Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes