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PERFECT Project - Part 2 - Study 2

Pulse EnRiched Food and Exercise Clinical Trials (PERFECT Project): Part 2 - Acute Effects of Pulse Ingredients in Food Products on Aerobic Endurance and Substrate Oxidation During Exercise, as Well as, the Blood Glucose, Insulin, Lactate and Food Intake Response Following an Endurance Exercise Session in Adults - Study 2

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02370927
Enrollment
30
Registered
2015-02-25
Start date
2016-05-31
Completion date
2017-12-31
Last updated
2023-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Prevention, Obesity Prevention

Brief summary

The objectives are to test the acute effects of different cereals 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. The investigators hypothesize that consumption of cereals 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. The investigators also hypothesize that consumption of cereals 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.

Interventions

OTHERControl

Non pulse extruded cereal

Pulse extruded cereal

Pulse extruded cereal

Pulse extruded cereal

Pulse extruded cereal

Pulse extruded cereal

Sponsors

Saskatchewan Pulse Growers
CollaboratorOTHER
Alberta Pulse Growers
CollaboratorOTHER
University of Manitoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Normoglycemic (\<5.6 mmol/L) and normotensive (systolic blood pressure \<140 mm Hg and diastolic blood pressure below \< 90 mm Hg) * Body Mass Index of 18.5-29.9 kg/m2

Exclusion criteria

* Restrained eaters * Regularly skip breakfast * Smokers * Those on medications that may influence study outcomes or have experienced any gastrointestinal related health conditions/surgeries over the past year * Those who are active (organized activities or athletic training at a high intensity; ≥ 150 minutes per week of moderate to vigorous physical activity) * Those unable to walk for an hour continuously

Design outcomes

Primary

MeasureTime frameDescription
Plasma Glucose Concentrations0-240 minutesMeasured in blood using intravenous catheter. Glucose will be determined by automated methods using Abbot Spectrum Clinical Chemistry-X Analyzer,
Food Intakeat 240 minutesAd-libitum meal
Subjective Appetite0-240 minutesMotivation-to-eat Visual Analog Scale questionnaire
Exercise intensity60-120 minutesOxygen consumption measured during exercise at 3 time points
Insulin concentrations0-240 minutesMeasured in blood using intravenous catheter. and Insulin will be measured by commercially available radioimmunoassay (RIA) kits

Secondary

MeasureTime frameDescription
Physical comfort measured by Visual Analog Scale questionnaire0-240 minutesContributions from energy intake
Palatability measured by Visual Analog Scale questionnaire5 and 260 minutesFood tasting
Energy/fatigue measured by Visual Analog Scale questionnaire0 - 240 minutesEstimate of energy expenditure
Heart rate60-120 minutesTo monitor exercise intensity and give a measure of fatigue (cardiovascular drift)
Substrate Oxidation60-120 minutesRespiratory quotient measured during exercise at 3 time points
Lactate concentration60-120 minutesMeasured before, during, and after exercise exercise at 3 time points

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026