Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 2:08 AM
Ignite Modification Date:
2025-12-25 @ 2:08 AM
NCT ID:
NCT04034160
Brief Summary:
The purpose of this graduate student research study is to compare the rise of serum lipids, glucose, and hs-CRP levels after consumption of a beef burger versus a vegetarian burger in healthy adults between the ages of 21 and 55
Detailed Description:
Visit 1
* Sign an informed consent.
* Complete a brief questionnaire about demographics (age, gender, and race), eating habits, physical activity level, and medical history (known allergies, and history of dyslipidemia, diabetes mellitus, or arthritis)
* Will be directed to fast for 8 hours prior to Visit 2. Visit 2
* Be randomized into either Group 1 or Group 2. One group will eat the beef burger first and the other group will eat the vegetarian burger first.
* Fill out a questionnaire on number of hours slept and current stress level.
* Take a finger prick test (tiny drop of blood) to determine baseline measurements for serum lipids, glucose, and hs-CRP levels.
* Consume either a beef burger or vegetarian burger.
* Afterwards, remain in Nichol Hall, Room A112, for 2 hours (may study, watch a movie, etc.).
* May not consume anything except for water.
* After 30 min, 60 min, 120 min, finger prick tests will be used to measure post-consumption serum lipids, glucose, and hs-CRP levels.
* Will be asked to try and identify burger consumed and rate the taste of the burger.
* Will be directed to fast for 8 hours prior to Visit 3. Visit 3
* Repeat the same procedure as Visit 2. However, this time the burgers will be switched.
Study:
NCT04034160
Study Brief:
Protocol Section:
NCT04034160