I. Research Objective: This study aims to evaluate the GI of Saskatoon berry powder and whole fruit in healthy individuals.
II. Methodology:
Study Design
* Type: Randomized, open-label study.
* Duration: Approximately 4 weeks for each participant.
* Setting: Clinical nutrition laboratory.
Participant Recruitment:
Following approval from the University of Manitoba Research Ethics Board, we will distribute recruitment materials across the university campus. Interested individuals may contact the research coordinator to express interest in participation.
Target enrollment: 10-20 participants
Eligibility Requirements:
* Individuals in good health (males and females)
* Between 18 and 74 years of age
* Body Mass Index (BMI) within the range of 18.5-29.9 kg/m²
* Free from diabetes, hyperlipidemia, and hypertension
* Must not be taking medications for diabetes, cholesterol, or blood pressure management.
Required Resources
* Saskatoon berry powder (Prairie Berry Inc.)
* Whole Saskatoon berries (Prairie Berry Inc.)
* Control substance: 25g glucose drink
* Glucose monitoring instruments
* Water (250ml) for powder administration Protocol Overview Visit #1: Initial Session: Research consent The research coordinator will conduct informed consent procedures at an agreed-upon location.
* Initial Assessment:
* Blood pressure measurement
* Heart rate monitoring
* Anthropometric measurements Visit #2: Primary Testing Session
* Preparation Guidelines:
* Fasting period: 10-14 hours overnight
* Session start: 9:00 AM
* Testing Protocol:
The participant will receive either Saskatoon berry powder (25g carbohydrate equivalent) with 250ml of water (consumption within 10 minutes), or whole Saskatoon berries (25g carbohydrate equivalent, consumption within 20 minutes) or glucose drink (25 g carbohydrate, consumption with in 10 min).
Blood glucose monitoring schedule:
Initial reading (0 min) 15 minutes post-consumption 30 minutes post-consumption 45 minutes post-consumption 60 minutes post-consumption 90 minutes post-consumption 120 minutes post-consumption Visit #3: Reference Food Assessment Participants will undergo an identical protocol with oral glucose drink (25g carbohydrate equivalent) 2-7 days following the initial assessment.
Important: A minimum 48-hour washout period is required between each test (control or berry preparation).
Analytical Methods The glycemic index will be determined through analysis of blood glucose area under curve (AUC), following established protocols (Brouns et al., 2005).
* GI will be calculated as the ratio of the incremental AUC (iAUC) for SB to the iAUC for glucose drink, multiplied by 100.
* Data will be presented as mean ± standard deviation.
* Paired t-tests or equivalent non-parametric tests will be used to compare iAUC between SB and glucose drink.
* A p-value \< 0.05 will be considered statistically significant.
