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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03941704
Other study ID # 609
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2019
Est. completion date June 30, 2021

Study information

Verified date October 2021
Source University of Saskatchewan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The hypothesis is that consumption of pulse-based foods (i.e. containing chickpeas, lentils, and split peas) during the workday will improve insulin sensitivity, glucose tolerance, blood lipids, body composition, and blood pressure in sedentary office workers.One-hundred office workers from a university campus will participate in a cross-over study where they will be randomized (i.e. assigned by chance) to receive pre-packaged pulse-based lunches and snacks to replace their usual lunches/snacks during the work day OR to continue consuming their usual diets for two months. After the first dietary intervention, they will undergo a 1-month "wash-out" and then participate in two months of the opposite dietary intervention. The main outcome to be assessed is change in glucose and insulin (i.e. blood sugar control) determined during an oral glucose tolerance test. Secondary outcomes include changes in body composition, lipids, and blood pressure. During the pulse-based diet phases, participants will be supplied with a ready-to-eat lunch and two snacks to eat during each workday. These will contain a total of 150g/d dry weight (250g/d wet weight) pulses


Description:

Sedentary behaviour has been deemed the "new smoking" based on multiple and potent negative impacts on health. Moreover, sedentary behaviour is a strong predictor of type 2 diabetes risk and cardiovascular disease. Previous studies have show that pulse-based meals derived from lentils, beans, chickpeas, and peas are effective for alleviating risk factors associated with diabetes and cardiovascular disease in clinical populations including older adults, overweight and obese individuals, and women with polycystic ovary syndrome; however, to date, there have been no nutrition-based interventions for alleviating risk factors for diabetes specifically targeting office workers exposed to long periods of sitting. Although people are aware of the health benefits of pulses, a major barrier to increased consumption continues to be a lack of knowledge on how to prepare pulse-based meals. This proposed study is designed to overcome this barrier. The main goal of this research study is to determine whether improvements in cardio-metabolic health can be realized by giving people pulse-based lunches and snacks to replace their regular workplace lunches and snacks. In this randomized controlled trial, 100 office workers from the University of Saskatchewan will participate in a cross-over study where they will be randomized into one of two diets for 2 months: Receive pre-packaged pulse-based lunches and snacks to replace their usual lunches/snacks during the work day OR to continue consuming their usual diets for two months. After a one-month washout, they will cross-over to the other condition. The primary outcome measure, Matsuda Index (determined by blood glucose and insulin responses to an oral glucose tolerance test), will be assessed before each diet phase and at the end (i.e. two months) of each diet phase. Secondary outcome measures (body composition, waist girth, lipids, blood pressure will also be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date June 30, 2021
Est. primary completion date May 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Men and Women - 18y or older - Engaged in >5 hours per day sitting Exclusion Criteria: - Diagnosed with diabetes - taking glucose or lipid-lowering medication - Regular consumers of pulses (1.5 cups (250g) or greater of pulses per week) - Engaged in 60 minutes or greater of physical activity per day

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Pulse-based diet
Low Glycemic Index
Regular diet
Moderate Glycemic Index

Locations

Country Name City State
Canada College of Kinesiology, University of Saskatchewan Saskatoon Saskatchewan

Sponsors (1)

Lead Sponsor Collaborator
University of Saskatchewan

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Insulin sensitivity Matsuda Index determined by glucose and insulin response to oral glucose tolerance test Change from baseline to 8 weeks
Secondary Glucose area under the curve Glucose area under the curve from a 2-hour oral glucose tolerance test Change from baseline to 8 weeks
Secondary Insulin area under the curve Insulin area under the curve from a 2-hour oral glucose tolerance test Change from baseline to 8 weeks
Secondary Fasting glucose Fasting glucose Change from baseline to 8 weeks
Secondary Fasting insulin Fasting insulin Change from baseline to 8 weeks
Secondary Low-density lipoprotein cholesterol LDL-C from fasting blood samples Change from baseline to 8 weeks
Secondary High-density lipoprotein cholesterol HDL-C from fasting blood samples Change from baseline to 8 weeks
Secondary Total cholesterol Total cholesterol from fasting blood samples Change from baseline to 8 weeks.
Secondary Triglycerides Triglycerides from fasting blood samples Change from baseline to 8 weeks
Secondary Waist Girth Waist Girth Change from baseline to 8 weeks
Secondary Fat mass Fat mass from DXA measurements Change from baseline to 8 weeks
Secondary Lean tissue mass Lean tissue mass from DXA measurements Change from baseline to 8 weeks
Secondary Systolic blood pressure Systolic blood pressure measured at rest Change from baseline to 8 weeks
Secondary Diastolic blood pressure Diastolic blood pressure measured at rest Change from baseline to 8 weeks
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