Pulse Revolution: Enhancing Metabolic Health Through the Power of Processed Chickpeas
NCT ID: NCT06758869
Last Updated: 2025-11-28
Study Results
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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NOT_YET_RECRUITING
NA
204 participants
INTERVENTIONAL
2026-01-31
2029-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Control
Base DGA diet with a standardized non-pulse product snack
Control
Participants will consume the Base DGA diet with a standardized non-pulse product snack.
Whole Chickpeas
Adjusted DGA diet with standardized whole chickpea snack
Whole Chickpeas
Participants will consume an adjusted DGA diet with a standardized whole chickpea snack.
Puréed Chickpeas
Adjusted DGA diet with standardized puréed chickpea snack
Puréed Chickpeas
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
100% Chickpea Flour Product
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.
Whole Chickpeas
Participants will consume an adjusted DGA diet with a standardized whole chickpea snack.
Puréed Chickpeas
Participants will consume an adjusted DGA diet with a standardized puréed chickpea snack.
100% Chickpea Flour Product
Participants will consume an adjusted DGA diet with a standardized 100% chickpea flour product snack.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
19 Years
60 Years
ALL
Yes
Sponsors
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USDA Grand Forks Human Nutrition Research Center
FED
Responsible Party
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Shanon Casperson
Research Biologist
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
Countries
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Central Contacts
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Facility Contacts
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Related Links
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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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