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NCT07227701 · ClinicalTrials.gov registry record · NA
A Comparison of Satiety Effects Two Commercially Available Snack Bars
A NA study of Satiety, sponsored by Indiana University.
- Active
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT07227701: Active NA study of Satiety, sponsored by Indiana University.
NCT07227701 is a NA study of Satiety that is active but no longer recruiting, run by Indiana University. The registered enrollment target is 150 participants, above the 65-participant average among 7 other Satiety trials with a reported enrollment target (131% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07227701, a NA study of Satiety, is active but no longer recruiting, sponsored by Indiana University.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
The researchers are investigating the satiety effects of two commercially available snack bars. Qualified participants are age 18-65 with a body mass index of 18.5 to 29.9 kilograms of body weight per meter squared in height who are in good metabolic health. Participants will engage in two study visits conducted at the Indiana University--Bloomington Innovation Center. Study visits are separated by a 1-14 day washout period. Prior to each study visit, participants are asked to engage in normal activity and to refrain from strenuous exercise. Furthermore, subjects are asked to consume a typical diet the day prior to the study visit with one caveat; they are to consume standard frozen dinners (evening meal) of their choosing between 7-8 PM and to remain fasted afterward except for water and non-caloric beverages until the study visit the following day. The amount of food provided for the evening meal is estimated using a standard calorie calculator based on the Mifflin-St. Jeor equation and an estimate of their activity level. Subjects are instructed to consume only as much of the provided food as needed to become comfortably full as they would ordinarily. Subjects record their diet for the day. Upon arrival at the Innovation Center between 8-8:40 AM, compliance with the prior day protocol is verified through interview, and the diet record is reviewed. Participants consume 300 kcal of snack bars and complete visual analogue scales to assess hunger, fullness, desire to eat, and satisfaction at fasting and at 30 minute intervals from the fasting measurement for 2 hours. Immediately after consuming the snack bars, subjects complete a sensory evaluation of the snack bars. Fifteen to thirty minutes after completion of the final visual analogue scale, subjects will be presented with an individual buffet which they consume ad libitum until comfortably full. A second study visit that mirrors the first but with different bars is conducted after the washout period (1-14 days
Primary Outcome
An individual buffet is provided in which participants consume as much food as they like until comfortably full. Buffet items include hamburgers, grilled chicken, buns, tomatoes, cheese, condiments (mayonnaise, mustard and ketchup), potato chips, mixed nuts, cookes, and a fruit tray of cantaloupe, watermelon, blueberries, strawberries, and pineapple with whipped cream offered as a condiment. Food are weighed before and after consumption of the buffet and macronutrient content is assessed from th
Conditions Studied
Interventions
- OTHER High carbohydrate snack bar
- OTHER High protein snack bar
Study Locations (1)
Indiana
- Indiana University--Bloomington School of Public Health - Bloomington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2025-02-27 |
| Est. Completion | 2026-03-31 |
| Phase | NA |
What the registry record for NCT07227701 still lists
NCT07227701 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, above the 65-participant average among 7 other Satiety trials with a reported enrollment target (131% higher).
The record links to 1 condition, with Satiety appearing as the primary indexed condition, and to 2 interventions - of which High carbohydrate snack bar is the first listed.
NCT07227701 reports a single indexed study location in Indiana.
Frequently Asked Questions
What is clinical trial NCT07227701 about?
NCT07227701 is a clinical study titled "A Comparison of Satiety Effects Two Commercially Available Snack Bars". The researchers are investigating the satiety effects of two commercially available snack bars. Qualified participants are age 18-65 with a body mass index of 18.5 to 29.9 kilograms of body weight per meter squared in height who are in good metabolic health. Participants will engage in two study vis...
What is the current status of trial NCT07227701?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2025-02-27. Estimated completion is 2026-03-31.
What conditions does trial NCT07227701 study?
This clinical trial studies the following conditions: Satiety.
What interventions are being tested in trial NCT07227701?
The interventions under investigation include: High carbohydrate snack bar (OTHER), High protein snack bar (OTHER).
Who is sponsoring clinical trial NCT07227701?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07227701 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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