Assessment of Glycemic Index for Dried Saskatoon Berries and Powder in Healthy Subjects
NCT ID: NCT06928688
Last Updated: 2026-01-08
Study Results
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Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2025-03-01
2025-11-20
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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SB powder
Volunteers drink 25 g of SB powder (25g carbohydrate equivalent) with 250ml water (consumption within 10 minutes)
Saskatoon berry powder
After oral intake of SB powder, dried whole SB fruit or glucose drink, finger tip blood glucose will be measured 15, 30, 45, 60, 90 and 120 minutes after the consumption.
Dried whole SB fruit
Volunteers intake Dried whole SB fruit (25g carbohydrate equivalent) within 20 minutes. Participants have option to choose intake one or both SB products. One week interval is required between the interventions.
Saskatoon berry powder
After oral intake of SB powder, dried whole SB fruit or glucose drink, finger tip blood glucose will be measured 15, 30, 45, 60, 90 and 120 minutes after the consumption.
Interventions
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Saskatoon berry powder
After oral intake of SB powder, dried whole SB fruit or glucose drink, finger tip blood glucose will be measured 15, 30, 45, 60, 90 and 120 minutes after the consumption.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Between 18 and 74 years of age
* Signed informed consent
Exclusion Criteria
* Diabetes, hyperlipidemia, and hypertension
* Taking medications for diabetes, cholesterol, or blood pressure
18 Years
74 Years
ALL
No
Sponsors
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University of Manitoba
OTHER
Responsible Party
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Locations
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University of Manitoba
Winnipeg, Manitoba, Canada
Countries
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References
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Brouns F, Bjorck I, Frayn KN, Gibbs AL, Lang V, Slama G, Wolever TM. Glycaemic index methodology. Nutr Res Rev. 2005 Jun;18(1):145-71. doi: 10.1079/NRR2005100.
Zhao R, Khafipour E, Sepehri S, Huang F, Beta T, Shen GX. Impact of Saskatoon berry powder on insulin resistance and relationship with intestinal microbiota in high fat-high sucrose diet-induced obese mice. J Nutr Biochem. 2019 Jul;69:130-138. doi: 10.1016/j.jnutbio.2019.03.023. Epub 2019 Apr 9.
Other Identifiers
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HS26810 (B2025:012)
Identifier Type: -
Identifier Source: org_study_id
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