Pulse Revolution: Enhancing Metabolic Health Through the Power of Processed Chickpeas

ConditionHealthy
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-60
SponsorUSDA Grand Forks Human Nutrition Research Center

About this trial

The purpose of this research is to test how processing can affect how one's body uses the nutrients in that food. For this study the researchers are examining how making different food products out of chickpeas, such as hummus or pasta, changes how one's body uses those foods for energy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

apparently healthy adults

BMI >18.5 or <35 kg/m2 (healthy body weight - class I obesity)

ability to understand and sign the consent form

availability of transportation (i.e., participants must provide their own transportation to the Center)

Disqualifiers

usual pulse consumption greater than DGA recommendation

inability or unwillingness to consume any of the provided foods

more than a 10% change in body weight within the past 2 months

actively trying to lose weight

Trial design

Design model

Parallel

Treatments tested in this trial

  • Control

    Other intervention

    Participants will consume the Base DGA diet with a standardized non-pulse product snack.

  • Whole Chickpeas

    Other intervention

    Participants will consume an adjusted DGA diet with a standardized whole chickpea snack.

  • Puréed Chickpeas

    Other intervention

    Participants will consume an adjusted DGA diet with a standardized puréed chickpea snack.

  • 100% Chickpea Flour Product

    Other intervention

    Participants will consume an adjusted DGA diet with a standardized 100% chickpea flour product snack.

Treatment groups

204 Participants
are divided into 4 treatment groups
Group A: ControlExperimental treatment 1 intervention
Group B: Whole ChickpeasExperimental treatment 1 intervention
Group C: Puréed ChickpeasExperimental treatment 1 intervention
Group D: 100% Chickpea Flour ProductExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Differences in substrate oxidation in response to eating differentially processed pulse-based food products

Using whole-room calorimetry, measure differences in fat, carbohydrate, and protein oxidation in response to daily consumption of whole chickpeas, pureed chickpeas, or chickpea-flour pasta compared to a control diet.

Time frame
12 weels
2

Change from Baseline in substrate oxidation after consuming differentially processed pulse-based food products for 12 weeks

Measure changes in fat, carbohydrate, and protein oxidation in response to consuming whole chickpeas, pureed chickpeas, or chickpea-flour pasta using whole room calorimetry

Time frame
12 weeks
3

Determine participant consumption practices and attitudes towards pulse consumption using a validated questionnaire

The questionnaire is designed to assess enjoyment (two items), sensory properties (eight items), perceived cooking abilities (ten items), perceived practical aspects (six items), perceived healthiness (two items), upbringing (two items), social influences (four items), and quality issues (six items) of pulse consumption.

Time frame
Baseline

Secondary outcomes

1

Changes in the colonic microbiota in response to consuming differentially processed pulse-based food products

Fecal samples will be collected at Baseline and then again at weeks 4, 8, and 12 to identify how the predominant colon bacteria phyla are effected by consuming whole chickpeas, pureed chickpeas, or chickpea-flour pasta for 12 weeks.

Time frame
12 weeks
2

Changes in me metabolic gene expression and metabolites in response to consuming differentially processed pulse-based food products.

Blood samples will be collected before and after consuming whole chickpeas, pureed chickpeas, or chickpeas-flour pasta for 12 weeks to identify how consuming these foods effect the expression genes involved with fat metabolism. This will be accomplished by combining the different snapshots provided from pre/post intervention metabolomic, transcriptomic, and proteomic analysis.

Time frame
12 weeks

Other outcomes

Sponsors and contacts

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