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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02365363
Other study ID # B2014:114-6
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date December 19, 2017

Study information

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

Clinical Trial Summary

The objectives are to test the acute effects of different bagels containing pulse ingredients on: 1) aerobic endurance and substrate oxidation during exercise 2) response of blood glucose, insulin and appetite to an aerobic exercise session, and 3) food intake two hours following the exercise session. We hypothesize that consumption of bagels containing pulse ingredients 60 minutes before exercise will increase aerobic endurance (lower oxygen consumption), decrease carbohydrate oxidation (greater respiratory quotient), and a reduction in lactate production during compared to the same exercise session following the ingestion of a non-pulse food. We also hypothesize that consumption of bagels containing pulse ingredients will lead to lower blood glucose, insulin, appetite and food intake, suggesting lower calorie compensation, following a 60-minute aerobic exercise session compared to the same exercise session following the ingestion of a non-pulse food.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 19, 2017
Est. primary completion date December 19, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility - Normoglycemic (<5.6 mmol/L) and normotensive (systolic blood pressure <140 mm Hg and diastolic blood pressure below < 90 mm Hg) - BMI of 18.5-29.9 kg/m2 Exclusion Criteria: - Restrained eaters - Regularly skip breakfast - Smokers - Those who are active (organized activities or athletic training at a high intensity; = 150 min per week of moderate to vigorous physical activity) - Those on medications that may influence study outcomes or have experienced any gastrointestinal related health conditions/surgeries over the past year - Those unable to walk for an hour continuously

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Control
Non pulse ingredient bagel
Pea flour
Pulse ingredient bagel
Pea fibre
Pulse ingredient bagel
Pea flour and pea fibre
Pulse ingredient bagel
Pea flour and pea protein
Pulse ingredient bagel
Pea flour + pea fibre + pea protein
Pulse ingredient bagel

Locations

Country Name City State
Canada Richardson Centre for Functional Foods and Nutraceuticals, University of Manitoba Winnipeg Manitoba

Sponsors (3)

Lead Sponsor Collaborator
University of Manitoba Alberta Pulse Growers, Saskatchewan Pulse Growers

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma Glucose and Insulin Concentrations Measured in blood using intravenous catheter. Glucose will be determined by automated methods using Abbot Spectrum CCX Analyzer, and Insulin will be measured by commercially available RIA kits 0-240
Primary Food Intake Ad-libitum meal 120 min
Primary Subjective Appetite Motivation-to-eat VAS questionnaire 0-240 min
Primary Exercise intensity Oxygen consumption measured during exercise at 3 time points 60-120 min
Secondary Palatability Measured by VAS questionnaire 5 and 260 min
Secondary Physical comfort Measured by VAS questionnaire 0-240 min
Secondary Energy/fatigue Measured by VAS questionnaire 0 - 240 min
Secondary Heart rate To monitor exercise intensity and give a measure of fatigue (cardiovascular drift) 60-120 min
Secondary Lactate concentration Measured before, during, and exercise exercise at 3 time points 60-120 min
Secondary Substrate Oxidation Respiratory quotient measured during exercise at 3 time points 60-120 min
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