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

NCT ID: NCT06758869

Last Updated: 2025-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

204 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-31

Study Completion Date

2029-12-31

Brief Summary

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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.

Detailed Description

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The overall objective is to determine the impact of daily consumption of processed pulse-based food products on metabolic health, specifically the physiological responses related to energy metabolism. The primary hypothesis is that consuming a serving of pulses daily for 12 weeks will improve metabolic responses related to energy metabolism, particularly fat oxidation and molecular adaptations related to fat and glucose metabolism, compared to current Dietary Guidelines for Americans (DGA) recommendations. Furthermore, we hypothesize that the degree of processing will influence these metabolic adaptations such that the daily consumption of 100% pulse flour food products will result in the greatest effect on fat oxidation and molecular adaptations related to fat and glucose metabolism followed by the pulse purée which will have a greater effect than the whole cooked pulse (100% pulse flour \> purée \> whole).

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Control

Base DGA diet with a standardized non-pulse product snack

Group Type EXPERIMENTAL

Control

Intervention Type OTHER

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

Whole Chickpeas

Adjusted DGA diet with standardized whole chickpea snack

Group Type EXPERIMENTAL

Whole Chickpeas

Intervention Type OTHER

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

Puréed Chickpeas

Adjusted DGA diet with standardized puréed chickpea snack

Group Type EXPERIMENTAL

Puréed Chickpeas

Intervention Type OTHER

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

100% Chickpea Flour Product

Adjusted DGA diet with standardized 100% chickpea flour product snack

Group Type EXPERIMENTAL

100% Chickpea Flour Product

Intervention Type OTHER

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

Interventions

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Control

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

Intervention Type OTHER

Whole Chickpeas

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

Intervention Type OTHER

Puréed Chickpeas

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

Intervention Type OTHER

100% Chickpea Flour Product

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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)
* non-smoking or do not use other tobacco products, including e-cigarettes
* not taking steroid-based medications
* not planning to or currently attempting to gain or lose weight
* not allergic to study foods
* willing to comply with study demands

Exclusion Criteria

* 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
* pregnancy or actively trying to get pregnant
* lactation
* uncontrolled hypertension (systolic \>160 mmHg or diastolic \>100 mmHg)
* diagnosed cardiovascular, pulmonary, skeletal and metabolic diseases
* HbA1c ≥ 5.7%
* complete blood count (CBC) outside of the normal range for a healthy adult
* history of gastrointestinal (GI) disorders (including Celiac's or Crohn's disease, irritable bowel syndrome, acid reflux, ulcerative colitis, chronic constipation or diarrhea, and lactose intolerance)
* using medications known to affect appetite, blood lipids, body composition, body weight, or food intake (appetite control drugs, steroids)
* cannot read or understand English
Minimum Eligible Age

19 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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USDA Grand Forks Human Nutrition Research Center

FED

Sponsor Role lead

Responsible Party

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Shanon Casperson

Research Biologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Shanon Casperson

Role: PRINCIPAL_INVESTIGATOR

USDA Grand Forks Human Nutrition Research Center

Locations

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USDA Grand Forks Human Nutrition Research Center

Grand Forks, North Dakota, United States

Site Status

Countries

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United States

Central Contacts

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Shanon Casperson, PhD

Role: CONTACT

701-795-8497

Facility Contacts

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Angela Scheett

Role: primary

701-795-8386

Related Links

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https://www.ars.usda.gov/plains-area/gfnd/gfhnrc/docs/nutrition-studies/nutrition-studies/

Grand Forks Human Nutrition Research Center Current Nutrition Studies

Other Identifiers

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GFHNRC514

Identifier Type: -

Identifier Source: org_study_id

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