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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05888779
Other study ID # GFHNRC156
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 23, 2023
Est. completion date September 2024

Study information

Verified date January 2024
Source USDA Grand Forks Human Nutrition Research Center
Contact Julie Hess, PhD
Phone 701.795.8146
Email julie.hess@usda.gov
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to conduct novel research on the relationship between blood sugar and cognition.


Description:

This study is an acute parallel study design with one intervention visit needed per participant. There are 2 groups and 80 participants will be randomized into each group. Following the consent process, participants in each group will be seated individually in quiet rooms, with written instructions, several magazines, and a mini-fridge with beverages containing 110-120 kcals/8 fl oz. Participants will be provided instructions for the study, stating, "The study we are conducting explores the relationship between blood glucose and cognitive abilities. After consuming food or drink, your body regulates your blood glucose. Physical exertion can also affect blood glucose. Therefore, we ask that you relax in this space for 10-15 minutes. You can read the provided magazines during this time. Drinking a beverage will bring your body's blood glucose into the right phase for our questionnaires. In the fridge are some beverages, and we ask that you drink something." After 10-15 minutes, participants will be given a cognitive test (a questionnaire on paper) and asked to complete as much of it as they can within 5 minutes. Then, moving to a separate area, weight and height measurements will be taken.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Healthy weight to overweight (BMI 18.5-29.9 kg/m2) - No food allergies or food intolerances - Healthy (no chronic disease) as determined by online questionnaire - Non-pregnant and non-lactating - Not currently dieting or planning to follow a special diet - Minimal restricted eating practices Exclusion Criteria: - Obesity (BMI = 30 kg/m2) - Pregnant or lactating - Currently dieting or planning to follow a special diet

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Beverage One (Milk)
Participant will consume beverage one (milk) and complete novel cognitive assessment questionnaire on paper.
Beverage Two (Juice)
Participant will consume beverage two (fruit drink) and complete novel cognitive assessment questionnaire on paper.

Locations

Country Name City State
United States USDA Grand Forks Human Nutrition Research Center Grand Forks North Dakota

Sponsors (1)

Lead Sponsor Collaborator
USDA Grand Forks Human Nutrition Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Written cognitive task results from novel cognitive assessment questionnaire. Results of cognitive task after consuming a study beverage (milk or fruit-flavored drink). More questions answered correctly results in a higher score. The assessment has a total of 10 questions, and participants will be asked to complete as much of this assessment as they can within a 5 minute timeframe. 10 minutes post beverage ingestion
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